BIOMIMETIC ICE-INHIBITING MATERIAL AND CRYOPRESERVATION SOLUTION COMPRISING SAME
20220192179 · 2022-06-23
Inventors
- Jianjun WANG (US)
- Shenglin JIN (US)
- Jianyong LV (US)
- Jie YAN (US)
- Jie QIAO (US)
- Liying YAN (US)
- Rong LI (US)
Cpc classification
G01N2015/0222
PHYSICS
A01N1/0221
HUMAN NECESSITIES
G16C60/00
PHYSICS
International classification
Abstract
A biomimetic ice growth inhibition material is prepared. by constructing a library for structures of compound molecules, with the compound molecules comprising a hydrophilic group and an ice-philic group, by evaluating the spreading performance of each compound molecule at an ice-water interface by adopting molecular dynamics simulation (MD simulation), and by screening the compound molecules with the desired affinities for ice and water. The present invention firstly provides the mechanism of the affinities of the ice growth inhibition material for ice and water, introduces MD simulation into the molecular structure design of the ice growth inhibition material, evaluates the affinities of the designed ice growth inhibition material for ice and water through MD simulation, predicts the ice growth inhibition performance of the ice growth inhibition material, and can realize the optimization of the structure.
Claims
1. A molecular design method for an ice growth inhibition material, comprising the following steps: (1) constructing a library for structures of compound molecules, wherein the compound molecules comprise a hydrophilic group and an ice-philic group; (2) simulating and evaluating the spreading performance of each of the compound molecules at an ice-water interface by adopting molecular dynamics (MD) simulation; and (3) screening the compound molecules with desired affinities for ice and water.
2. The molecular design method according to claim 1, wherein the MD simulation of the step (2) is performed by GROMACS, AMBER, CHARMM, NAMD, or LAMMPS; preferably, in the MD simulation of the step (2), a model of a water molecule is selected from models of TIP3P, TIP4P, TIP4P/2005, SPC, TiP3P, TIP5P and SPC/E, preferably TIP4P/2005 model of a water molecule; preferably, in the MD simulation of the step (2), a force field parameter is provided by one of GROMOS, ESFF, MM force field, AMBER, CHARMM, COMPASS, UFF, CVFF and other force fields.
3. The molecular design method according to claim 1, wherein in the MD simulation of the step (2), simulation and calculation are performed on interactions between the compound molecules, interactions between the compound molecules and the water molecules, and interactions between the compound molecules and ice-water molecules; for example, the interactions include the formation of a hydrogen bond, a Van der Waals interaction, an electrostatic interaction, a hydrophobic interaction, a π-π interaction and the like.
4. The molecular design method according to claim 1, wherein in the MD simulation of the step (2), a temperature and pressure are adjusted when the simulation and calculation are performed on the interactions between the molecules; preferably, the temperature and the pressure are adjusted by using a V-rescale temperature regulator and a pressure regulator; preferably, in the MD simulation of the step (2), a molecular configuration of the compound molecules is maintained by selecting a potential energy parameter; preferably, in the step (2), periodic boundary conditions are adopted for x-direction, y-direction and z-direction when an aqueous solution system is simulated; periodic boundary conditions are adopted for x-direction and y-direction when an ice-water mixed system is simulated; preferably, in the MD simulation of the step (2), a cubic or octahedral box of water is selected, and a cubic box of water with dimensions of 3.9×3.6×1.0 nm.sup.3 is preferred.
5. The molecular design method according to claim 1 4, wherein a main chain of the compound molecules is a carbon chain or peptide chain structure.
6. The molecular design method according to claim 1, wherein the hydrophilic group is a functional group capable of forming a non-covalent interaction with a water molecule, for example, forming a hydrogen bond, a Van der Waals interaction, an electrostatic interaction, a hydrophobic interaction or a π-π interaction with water; for example, the hydrophilic group may be selected from at least one of hydroxyl (—OH), amino (—NH.sub.2), carboxyl (—COOH) and amino (—CONH.sub.2), or, for example, from a compound molecule, such as a hydrophilic amino acid such as proline (L-Pro), arginine (L-Arg) and lysine (L-Lys), glucono delta-lactone (GDL) and a saccharide, and a molecular fragment thereof; the ice-philic group is a functional group capable of forming a non-covalent interaction with ice, for example, forming a hydrogen bond, a Van der Waals interaction, an electrostatic interaction, a hydrophobic interaction or a π-π interaction with ice; illustratively, the ice-philic group may be selected from hydroxyl (—OH), amino (—NH.sub.2), phenyl (—C.sub.6H.sub.5), pyrrolidinyl (—C.sub.4H.sub.8N) and the like, or, for example, from a compound molecule, such as an ice-philic amino acid such as glutamine threonine (L-Thr) and aspartic acid (L-Asn), a benzene ring (C.sub.6H.sub.6) and pyrrolidine (C.sub.4H.sub.9N), and a molecular fragment thereof.
7. The molecular design method according to claim 1, wherein the ice growth inhibition material is formed by covalently bonding a block comprising a hydrophilic group to a block comprising an ice-philic group, or is formed by ionically bonding a molecule comprising a hydrophilic group to a molecule comprising an ice-philic group.
8. The molecular design method according to claim 1, further comprising a step of synthesizing the compound molecules, for example polymerization, dehydration condensation, or biological fermentation of genetically engineered bacteria.
9. An ice growth inhibition material obtained by the molecular design method according to claim 1.
10. The ice growth inhibition material according to claim 9, wherein the ice growth inhibition material is a PVA with a diad syndiotacticity r of 45%-60% and a molecular weight of 10-500 kDa; preferably, the PVA has a diad syndiotacticity r of 50%-55% and a molecular weight of 10-30 kDa.
11. A method for screening an ice growth inhibition material, comprising: (1) determining the affinity of the ice growth inhibition material for water; and (2) determining the spreading performance of the ice growth inhibition material at an ice-water interface.
12. The method for screening an ice growth inhibition material according to claim 11, wherein the step (1) is achieved by determining the solubility, the hydration constant, the dispersion size of the ice growth inhibition material in water, and/or the number of intermolecular hydrogen bonds formed between a molecule of the ice growth inhibition material and a water molecule.
13. The method for screening an ice growth inhibition material according to claim 11, wherein the step (2) is achieved by determining the amount of the ice growth inhibition material absorbed on an ice surface by an ice adsorption experiment, the amount of the ice growth inhibition material absorbed on the ice surface=(the mass m.sub.1 of the ice growth inhibition material adsorbed on the ice surface/the total mass m.sub.2 of the ice growth inhibition material in an original solution comprising the ice growth inhibition material)×100%.
14. The method for screening an ice growth inhibition material according to claim 11, wherein the ice adsorption experiment comprises: S1, preparing an aqueous solution of the ice growth inhibition material, and cooling to a supercooling temperature; S2, placing a pre-cooled temperature-regulating rod in the aqueous solution to induce an ice layer to grow on the surface of the temperature-regulating rod, continuously stirring the aqueous solution to enable the ice growth inhibition material to be gradually adsorbed onto the surface of the ice layer, and keeping the temperature of the temperature-regulating rod and the temperature of the aqueous solution at a supercooling temperature; and S3, determining the amount of the ice growth inhibition material absorbed on the ice surface; preferably, the temperature-regulating rod is pre-cooled in one of modes of freezing by liquid nitrogen, dry ice or an ultra-low temperature refrigerator, preferably, wherein the supercooling degree and the adsorption time are maintained unchanged during the ice adsorption experiment to ensure that the surface area of the resulting ice is maintained unchanged within an allowable error range, preferably, wherein the method is used for screening the material. for inhibiting the growth of ice crystals, and preferably, further comprising a step (3): evaluating the affinity of the material for water and the affinity of the material for ice, wherein the material with strong affinities for water and ice has good ice growth inhibition performance.
15. (canceled)
16. The method for screening an ice growth inhibition material according to claim 14, wherein the ice growth inhibition material in the step S1 is fluorescently pre-labeled, for example, with fluorescein; preferably, if the ice growth inhibition material itself has absorption characteristics in an ultraviolet or fluorescence spectrum, no fluorescent label is required preferably, the step S3 comprises: S3a, taking out an ice block after adsorption, rinsing the ice block with purified water, and melting the ice block to give an adsorption solution of the ice growth inhibition material; and S3b, determining the volume V of the melted adsorption solution of the ice growth inhibition material, determining the mass/volume concentration c of the ice growth inhibition material in the adsorption solution and calculating the mass m.sub.1 of the ice growth inhibition material adsorbed on the ice surface through the formula m.sub.1=eV, preferably, in the S3b, the concentration c is determined by ultraviolet-visible spectroscopy.
17-20. (canceled)
21. An ice adsorption experimental device for use in the method according to claim 13, or comprising a multilayer liquid storage cavity, a temperature-regulating rod and a temperature regulator, wherein the multilayer liquid storage cavity sequentially comprises an ice adsorption cavity, a bath cavity and a cooling liquid storage cavity from inside to outside, the temperature-regulating rod being arranged in the ice adsorption cavity, and the temperatures of the temperature-regulating rod and the liquid storage cavity being regulated by the temperature regulator, wherein, preferably, the temperature-regulating rod is of a hollow structure made of a thermally conductive material, and the hollow structure of the temperature-regulating rod is provided with a liquid inlet and a liquid outlet; the temperature regulator is a fluid temperature regulator and is provided with a cooling liquid outflow end and a reflux end; two ends of the cooling liquid storage cavity is provided with a liquid inlet and a liquid outlet: the cooling liquid outflow end of the temperature regulator, the liquid inlet of the temperature-regulating rod, the liquid outlet of the temperature-regulating rod, the liquid inlet of a cooling liquid storage tank, the liquid outlet of the cooling liquid storage tank and the reflux end of the temperature regulator are sequentially linked via pipelines through which a cooling liquid flows; preferably the multilayer liquid storage cavity is provided with a cover; preferably, when the ice adsorption experimental device is used, the ice adsorption cavity is arranged to contain the aqueous solution of the ice Growth inhibition material, and the bath cavity in the middle layer is arranged to contain a bath medium that is at a preset temperature, for example, a water bath, an ice bath or an oil bath; after the preset temperature of the cooling liquid is reached, the cooling liquid flows out through the temperature regulator and flows into the hollow structure of the temperature-regulating rod to regulate the temperature of the temperature-regulating rod, then flows out from the liquid outlet of the temperature-regulating rod and flows into the cooling liquid storage cavity in the outer layer to maintain the temperature of the bath medium at the preset level. and then flows through the liquid outlet of the cooling liquid storage tank and the reflux end of the temperature regulator and enters the temperature regulator to circulate.
22. (canceled)
23. A cryopreservation solution, comprising the biomimetic ice growth inhibition material according to claim 9, preferably, wherein the biomimetic ice growth inhibition material is one of or a combination of a. polyvinyl alcohol (PVA), an amino acid or a polyamino acid, and/or a peptidic compound; the cryopreservation solution further comprises a polyol, a water-soluble saccharide (or a derivative thereof such as water-soluble cellulose) and a buffer, preferably, the cryopreservation solution comprises the peptidic compound, and specifically comprising, per 100 mL, 0.1-50 g of the peptidic compound, 0-6.0 g of the PVA, 0-9.0 g of the polyamino acid or the amino acid, 0-15 mL of DMSO, 5-45 mL of the polyol, the water-soluble saccharide at 0.1-1.0 mol.Math.L.sup.−1, 0-30 mL of serum and the balance of the buffer, preferably, the cryopreservation solution comprises the PVA, and specifically comprising, per 100 mL, 0.01-6.0 g of the PVA, 0-50 g of the peptidic compound, 0-9.0 g of the polyamino acid or the amino acid, 0-15 mL of DMSO, 5-45 mL of the polyol, the water-soluble saccharide at 0.1-1.0 mol.Math.L.sup.−1, 0-30 mL of serum and the balance of the buffer, preferably, the cryopreservation solution comprises the amino acid or the polyamino acid, and specifically comprising, per 100 mL. 0.1-50 g of the amino acid or the polyamino acid, 0-6.0 g of the PVA, 0-15 mL of DMSO, 5-45 mL of the polyol, the water-soluble saccharide at 0.1-1.0 mol.Math.L.sup.−1, 0-30 mL of serum and the balance of the buffer, preferably, the content of the amino acid and/or the polyamino acid in the cryopreservation solution is 0.5-50 g preferably 1.0-35 g, per 100 mL; for example, the content of the amino acid may be 5.0-35 g, preferably 15-25 g, in the presence of the amino acid; the content of the polyamino acid may be 0.5-9.0 g preferably 1.0-5.0 g, in the presence of the polyamino acid, preferably, the polyol may be a polyol having 2-5 carbon atoms, preferably a diol having 2-3 carbon atoms, and/or a triol, such as any one of ethylene glycol, propylene glycol and glycerol, preferably ethylene glycol; preferably, the content of the polyol in the cryopreservation solution is 5.0-40 mL, for example, 6.0-20 mL, 9-15 mL, per 100 mL, the cryopreservation solution comprises preferably, the water-soluble saccharide is at least one of a non-reducing disaccharide. a water-soluble polysaccharide, a water-soluble cellulose and a saccharide anhydride, and, for example, is selected from sucrose, trehalose, hydroxypropyl methylcellulose and polysucrose. preferably, wherein the buffers may be selected from at least one of DPBS, hepes-buffered HTF and other cell culture buffers. preferably, wherein the content of the DMSO in the cryopreservation solution is 0-10 mL, for example, 1.0-7.5 mL, per 100 mL; the content of the serum in the cryopreservation solution is 0.1-30 ML, for example, 5.0-20 mL, per 100 mL; the content of the water-soluble saccharide in the cryopreservation solution is 0.1-1.0 mol.Math.L.sup.−1, for example, 0.1-0.8 mol.Math.L.sup.−1, per 100 mL; the content of the polyol in the cryopreservation solution is 5.0-40 mL, for example. 6.0-20 mL, per 100 mL, preferably, the pH is 6.5-7.6, preferably, the PVA is selected from one of or a combination of two or more of an isotactic PVA, a syndiotactic PVA and an atactic PVA. and for example, the PVA has a diad syndiotacticity of 15%-65%, preferably a diad syndiotacticity of 45%-65%, preferably, the PVA may be selected from a PVA having a molecular weight of 10-500 kDa or higher, preferably, the peptidic compounds are obtained by reacting ice-philic amino acids, such as threonine (L-Thr), glutamine (L-Gln) and aspartic acid (L-Asn), with other hydrophilic amino acids that may be selected from arginine, proline and alanine, or glucono delta-lactone (GDL) or saccharides, preferably, the peptidic compound consists of no less than two amino acid units, such as 2-8 amino acid units. preferably the peptidic compound has a structure of any one of formula (1) to formula (9): ##STR00006## ##STR00007## wherein R in the formula (9) is selected from substituted or unsubstituted alkyl, and the substituent may be selected from —OH, —NH.sub.2, —COOH, —CONH.sub.2 and the like; for example, R is substituted or unsubstituted C.sub.1-6 alkyl, and preferably R is —CH.sub.3, —CH.sub.2CH.sub.3, —CH.sub.2CH.sub.2 COOH; n is an integer no less than 1 and no more than 1000, and preferably, the amino acid is an amino acid comprising an ice-philic group and a hydrophilic group, the polyamino acid is a polyamino acid consisting of an amino acid comprising an ice-philic group and an amino acid comprising a hydrophilic group, and the polyamino acid preferably has a degree of polymerization of 2-40, for example a degree of polymerization of 6, 8, 15 and 20 and the like, and for example, is one of or a combination of two or more of poly-L-proline, poly-L-arginine; the amino acid is selected from one or two of arginine, threonine, proline, lysine, histidine glutamic acid. aspartic acid, glycine and the like, such as a combination of arginine and threonine; or a polyamino acid consisting of the above amino acids.
24-39. (canceled)
40. A freezing equilibration solution, comprising, per 100 mL, 5.0-45 mL of a polyol and the balance of a buffer, optionally comprises 0-15 mL of DMSO, 0-30 mL of serum, and/or 0-5 of a PVA.
41. (canceled)
42. A cryopreservation reagent, comprising the cryopreservation solution according to claim 23.
43. Use of the cryopreservation solution according to claim 23 for cryopreservation of cells, tissues and organs, wherein, preferably, the cells are germ cells or stem cells; for example. the germ cells are selected from oocytes and sperms, and the stem cells are selected from embryonic stem cells, various mesenchymal stern cells (for example umbilical cord mesenchymal stem cells, adipose mesenchymal stem cells and bone marrow mesenchymal stem cells), and hematopoietic stem cells, or the tissue is an ovarian tissue or embryonic tissue, wherein the organ is an ovarian organ.
44-46. (canceled)
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION
[0154] The preparation method of the present invention will be further illustrated in detail with reference to the following specific examples. It should be understood that the following examples are merely exemplary illustration and explanation of the present invention, and should not be construed as limiting the protection scope of the present invention. All techniques implemented based on the afore-mentioned contents of the present invention are encompassed within the protection scope of the present invention.
[0155] Unless otherwise stated, the experimental methods used in the following examples are conventional methods. Unless otherwise stated, the reagents, materials, and the like used in the following examples are commercially available.
A. Molecular Design of Ice Growth Inhibition Material
[0156] The core molecule of the ice growth inhibition material disclosed herein can be designed to various groups having an affinity for water and groups having an affinity for ice, which are linked by covalent bonds or non-covalent bonds such as ionic bonds.
[0157] The molecular design method for the ice growth inhibition material disclosed herein comprises the following steps:
[0158] (1) constructing a library for structures of compound molecules, wherein the compound molecules comprise a hydrophilic group and an ice-philic group;
[0159] (2) simulating and evaluating the spreading performance of each of the compound molecules at an ice-water interface by adopting molecular dynamics (MD) simulation; and
[0160] (3) screening the ice growth inhibition molecule with desired affinities for ice and water.
[0161] According to the present invention, the main chain of the ice growth inhibition molecule is a carbon chain or a peptide chain.
[0162] According to the present invention, the MD simulation of the step (2) can be performed by GROMACS, AMBER, CHARMM, NAMD, or LAMMPS.
[0163] According to the present invention, in the MD simulation of the step (2), a model of a water molecule may be selected from models of TIP3P, TIP4P, TIP4P/2005, SPC, TIP3P, TIP5P, and SPC/E, preferably TIP4P/2005 model of a water molecule.
[0164] According to the present invention, in the MD simulation of the step (2), a force field parameter is provided by one of GROMOS, ESFF, MM force field, AMBER, CHARMM, COMPASS, UFF, CVFF and other force fields.
[0165] According to the present invention, in the MD simulation of the step (2), simulation and calculation are performed on interactions between ice growth inhibition molecules, interactions between ice growth inhibition molecules and water molecules, and interactions between ice growth inhibition molecules and ice-water molecules. The interactions include the formation of a hydrogen bond, a Van der Waals interaction, an electrostatic interaction, a hydrophobic interaction, a 7C-7C interaction and the like.
[0166] According to the present invention, in the MD simulation of the step (2), when the simulated and calculated molecules interact, the temperature and pressure are adjusted. In one embodiment of the present invention, a V-rescale (modified Berendsen) temperature-regulator and a pressure-regulator are used to regulate the temperature and pressure.
[0167] According to the present invention, in the MD simulation of the step (2), the molecular configuration of the compound molecule is maintained by selecting a potential energy parameter. Preferably, the potential energy parameter is selected, so that the molecular configuration of the compound molecule is maintained at a higher temperature.
[0168] According to the present invention, in the step (2), periodic boundary conditions are adopted for x-direction, y-direction and z-direction when an aqueous solution system is simulated; periodic boundary conditions are adopted for x-direction and y-direction when an ice-water mixed system is simulated.
[0169] According to the present invention, in the MD simulation of the step (2), a cubic or octahedral box of water is selected, and a cubic box of water with dimensions of 3.9×3.6×1.0 nm.sup.3 is preferred.
[0170] As a specific embodiment of the present invention, during the process of molecular dynamics calculations of the MD simulation, the V-rescale (modified Berendsen) temperature-regulator and the pressure-regulator regulate the temperature and pressure.
[0171] In the MD simulation and calculations, the main criterion for determining the existence of a hydrogen bond is the energy criteria or the geometric criteria, preferably, the geometrical criteria; when the distance (pitch) between oxygen atoms is less than 0.35 nm and the angle HO . . . H is less than 30 degrees, a hydrogen bond between two hydroxyl groups or between a hydroxyl group and a water molecule is formed.
[0172] As a specific embodiment of the present invention, the ice growth inhibition material may be a compound that has a carbon chain as the main chain and is substituted with an ice-philic group and a hydrophilic group; the ice growth inhibition material may comprise a group that is both hydrophilic and ice-philic, such as hydroxyl and amino groups, and may further comprise an ice-philic group and a hydrophilic group separately. For example, the molecular structure of the ice growth inhibition material is designed to have a repeating unit —[CH.sub.2—CHOH]—.
[0173] In an embodiment of the present invention, the molecule of the ice growth inhibition material is a PVA. The PVA is selected from one of or a combination of two or more of an isotactic PVA, a syndiotactic PVA and an atactic PVA. For example, the PVA has a diad syndiotacticity of 15%-65%, specifically, for example, 40%-60% and 53%-55%. Atactic PVA is preferred, for example, the PVA with a diad syndiotacticity of 45%-65%. The PVA may be selected from a PVA having a molecular weight of 10-500 kDa or higher, such as 10-30 kDa, 30-50 kDa, 80-90 kDa, and 200-500 kDa. The PVA may be selected from a PVA having a degree of hydrolysis of greater than 80%, for example, 80%-99%, 82%-87%, 87%-89%, 89%-99%, and 98%-99%.
[0174] In an embodiment of the present invention, the molecule of the ice growth inhibition material is a peptidic compound. The peptidic compounds are obtained by reacting ice-philic amino acids, such as threonine (L-Thr), glutamine (L-Gln) and aspartic acid (L-Asn), with other hydrophilic amino acids that may be selected from arginine, proline, alanine, and the like, or GDL or saccharides. The peptidic compound consists of no less than two amino acid units, such as: 2-8 amino acid units, specifically, 2-5, such as 2, 3, 4, 5 and 6 amino acid units; each amino acid unit is different. In the peptidic compound, the molar ratio of the ice-philic amino acid such as threonine to other hydrophilic amino acids is (0.1-3):1, preferably (0.5-2):1. The arrangement of the ice-philic amino acid and other hydrophilic amino acids in the peptidic compound is not particularly limited, and may be linked by using the amino acid linking groups or chemical bonds known in the art. For example, the ice-philic amino acid and the hydrophilic amino acid may be alternately arranged, or multiple ice-philic amino acids or hydrophilic amino acids are linked to form a fragment of the ice-philic amino acid or the hydrophilic amino acid, which is then linked to the hydrophilic amino acid (or a fragment) or the ice-philic amino acid (or a fragment), respectively. In an embodiment of the present invention, the peptidic compound is at least one of L-Thr-L-Arg (TR), L-Thr-L-Pro (TP), L-Arg-L-Thr (RT), L-Pro-L-Thr (PT), L-Thr-L-Arg-L-Thr (TRT), L-Thr-L-Pro-L-Thr (TPT), L-Ala-L-Ala-L-Thr (AAT) and L-Thr-L-Cys-L-Thr (TCT). In another embodiment, the peptidic compound is a GDL-L-amino acid, such as GDL-L-Thr, GDL-L-Ser or GDL-L-Val.
[0175] In yet another embodiment, the peptidic compound has any one of the structures of formula (1) to formula (8):
##STR00001##
[0176] The above-mentioned peptidic compounds can be synthesized using a polypeptide synthesis method known in the art, such as a solid-phase synthesis method.
[0177] The preparation method disclosed herein comprises the following steps: resin swelling, covalently linking an amino acid whose the amino group is protected to the swollen resin, deprotecting, adding another amino acid whose the amino group is protected for condensation reaction, deprotecting, cleavaging and purifying.
[0178] The glycopeptide derivative can be prepared by using the known method for reacting an amino acid with a saccharide. For example, the glycopeptide derivative can be prepared by reacting glucono delta-lactone or other saccharides with an amino acid in an organic solvent, or by using a solid-phase synthesis method. Glucono delta-lactone (GDL) is dissolved in an organic solvent, an amino acid and an alkaline catalyst are added to an organic solvent, and then the resulting mixture is added to the GDL solution to react at 55-60° C. after the amino acid and the alkaline catalyst are completely dissolved, after the reaction is finished, a white precipitate is filtered out, and the filtrate is evaporated to dryness to give a crude product.
[0179] According to the preparation method disclosed herein, the organic solvent may be selected from methanol, ethanol and the like.
[0180] In one embodiment, the glycopeptide derivative is prepared by using a solid-phase synthesis method comprising: resin swelling, covalently linking an amino acid where the amino group is protected to the swollen resin, deprotecting, adding a saccharide (such as ring-opened GDL) for condensation reaction, cleavaging, and purifying. GDL-L-Val and GDL-L-Ser were synthesized with reference to the method for synthesizing GDL-L-Thr.
[0181] The present invention further provides a peptidic compound of formula (9):
##STR00002##
wherein R is selected from substituted or unsubstituted alkyl, and the substituent may be selected from —OH, —NH.sub.2, —COOH, —CONH.sub.2 and the like; for example, R is substituted or unsubstituted C.sub.1-6 alkyl, and preferably R is —CH.sub.3, —CH.sub.2CH.sub.3, —CH.sub.2CH.sub.2 COOH; n is an integer no less than 1 and no more than 1000, and for example, may be an integer ranging from 1 to 100. In some embodiments of the present invention, n is an integer such as 2, 3, 4, 5, 6, 7, 8, 9 and 10.
[0182] As an embodiment of the present invention, the compound of formula (9) has a structure shown in any one of the following:
##STR00003##
[0183] According to the present invention, the compound of formula (9) is prepared by using the following synthetic route:
##STR00004##
[0184] In an embodiment of the present invention, the molecule of the ice growth inhibition material is an amino acid or a polyamino acid. The present invention further provides use of the above-mentioned molecule of the ice growth inhibition material, such as the PVA, the peptidic compound, the amino acid and the polyamino acid for controlling the growth of ice crystals in an aqueous solution, and use of the peptidic compound for preparing a cryopreservation solution for cells or tissues.
[0185] The ice growth inhibition materials designed and prepared according to the present invention, such as the PVA, the peptidic compound, the amino acid and the polyamino acid, are used for preparing a cryopreservation solution for cryopreservation of cells, tissues, organs and the like.
Example 1
(1) Molecular Structure Design of Compound:
[0186] Compound molecules having the repeating unit —[CH.sub.2—CHOH]— were designed to give a library for molecular structures that includes molecular models of an atactic and isotactic PVA.
(2) MD Simulation Experiment
[0187] The differences in the affinities of the atactic PVA and the isotactic PVA for ice and water were predicted by MD simulation experiments. [0188] a. MD simulation was performed by GROMACS 5.1, and the model of water was TIP4P/2005, which has a melting point of about 252.5 K. The interaction parameters of the PVA molecules were provided by the GROMOS54A7 force field, and the leapfrog integration algorithm with an integration step size of 2 fs was adopted. The electrostatic interaction was calculated by the PME method, and the cutoff radii of the coulomb potential and the L-J potential were both 1.0 nm. A V-rescale (modified Berendsen) temperature-regulator and a pressure-regulator were used to regulate the temperature and pressure. The time constant was set to 0.1 ps. [0189] b. Molecular chains of compounds having 7 repeating units were simulated and selected for investigation. The topology files of the PVA molecules were generated through ATB, and in order to maintain the tacticities of the two PVA molecules, the dihedral angle potential functions of the carbon chains of the molecules were required to be adjusted correspondingly. [0190] c. Periodic boundary conditions were adopted for x-direction, y-direction and z-direction when an aqueous solution system of the PVAs was simulated; periodic boundary conditions were adopted for x-direction and y-direction when an ice-water mixed system was simulated. All systems were simulated for 120 ns, and data from the last 60 ns were used for analysis.
[0191] The aqueous solution system of the molecules was first investigated. In a system having only one PVA chain, 1491 water molecules in total were used, the pressure was 1 atm, and the temperatures were 240 K, 250 K, 260 K, 270 K, 300 K, and 330 K.
[0192] In a system for investigating interactions of PVA molecules with ice, 6 PVA molecular chains were placed in a box of water with dimensions of 3.9 x 3.6 x 1.0 nm.sup.3, an ice block comprising 1100 water molecules was equilibrated at 240 K for 10 ns, and the ice block was placed under the box of water along the z-axis. The size of the mixed system in the z-direction was increased to 10 nm, and the ice-water mixed system was placed at the center of the box of water.
[0193] The topology files of the PVA molecules were generated through ATB, and the topology files were directly used. In order to maintain the tacticities of the two PVA molecules, the potential energy parameters were set to be 50 kcal/mol, so that the molecular configurations of the two PVA molecules can be maintained even at a higher temperature.
[0194] Molecular structure models of the two PVAs by MD simulation are shown in
(3) Evaluation of Simulation
[0195] The a-PVA can effectively generate hydrogen bonding with an ice surface and thus be adsorbed on the ice surface because the distance of three times the distance between adjacent OH matches the size of the ice crystal lattice. The i-PVA only changes the direction of the hydroxyl group without changing the distance between adjacent OH, so that the i-PVA and the a-PVA have similar ice adsorption ability. Meanwhile, according to the MD simulation results, the number of the intermolecular hydrogen bonds formed between the a-PVA and water molecules is more than that of the intermolecular hydrogen bonds formed between the i-PVA and water molecules, which indicates that the affinity of the a-PVA for water is stronger than that of the i-PVA. In addition, the states of 6 PVA molecular chains at an ice-water interface simulated by the MD simulation show that, the a-PVA tends to spread at an ice-water interface due to its good affinities for both ice and water while the i-PVA tends to aggregate at an ice-water interface due to its weaker affinity for water (
TABLE-US-00001 TABLE 1 a-PVA i-PVA Intramolecular Intermolecular Intramolecular Intermolecular hydrogen hydrogen hydrogen hydrogen T/K. bonding bonding bonding bonding 240 0.72(0.12) 6.76(0.43) 1.67(0.20) 5.92(0.42) 250 0.73(0.13) 6.87(0.32) 1.63(0.20) 5.95(0.36) 260 0.74(0.14) 6.83(0.35) 1.59(0.16) 6.04(0.35) 270 0.70(0.11) 6.87(0.30) 1.54(0.18) 6.13(0.34) 300 0.70(0.12) 6.74(0.35) 1.50(0.19) 6.09(0.28) 330 0.70(0.14) 6.54(0.33) 1.45(0.18) 6.05(0.31)
[0196] The MD simulation shows the contactable areas of the two PVAs with water molecules at an ice-water interface at 240 K, in which the contactable area of a-PVA is larger than that of the i-PVA, which further confirms that the spreading performance of the a-PVA at an ice-water interface is better than that of the i-PVA (see
[0197] Therefore, multiple results of the MD simulation show that the a-PVA has better spreading performance at an ice-water interface due to a strong affinity of its molecular structure for water molecules, and thus has a better ice growth inhibition effect than the i-PVA.
(4) Synthesis of Designed PVA Molecules
[0198] (4.1) Preparation of atactic polyvinyl alcohol a-PVA: the molecular weight is about 13-23 kDa, and the diad syndiotacticity r is about 55%
[0199] Vinyl acetate (VAc, Sigma-Aldrich) from which the inhibitor had been removed was dissolved in 100 mL of a solvent (methanol) in a 250 mL round-bottom flask under argon atmosphere to give a 25%-45% solution of VAc. After being cooled to -5° C., the reaction solution was carefully added dropwise with 80 mM of 2,2′-Azobis(2-methylpropionitrile) (Sigma-Aldrich). After being left to warm to room temperature, the above solution was stirred for 15 h, and the reaction solution was dissolved with 1 L of acetone and added dropwise to methanol to give a white precipitate. The above precipitate was washed with methanol, filtered and dried in an oven at 60° C. under vacuum for 6.0 h to give a white solid. The white solid was dissolved in a methanol solution (10 wt. %), and argon gas was introduced to remove oxygen from the solution. A 25% methanol solution of potassium hydroxide was added dropwise to the above solution and stirred for 4 h. After the stirring, the reaction solution was dissolved in a 2 M hydrochloric acid solution and added to a 2.0 M methanol solution of ammonia for precipitation to give an atactic polyvinyl alcohol (a-PVA). The proton NMR spectrum (
(4.2) Preparation of isotactic polyvinyl alcohol i-PVA: the molecular weight is about 14-26 kDa, and the isotacticity m is about 84%
[0200] a. Preparation of poly-tent-butyl vinyl ether (PBVE). Tert-butyl vinyl ether (t-BVE, Sigma-Aldrich) was dissolved in 100 mL of dry toluene in a 250 mL round-bottom flask under argon atmosphere to give a 2.5% toluene solution of t-BVE. After being cooled to −78° C., the above solution was carefully added dropwise with 0.2 mM boron trifluoride diethyl ether (BF.sub.3.Math.OEt.sub.2, Sigma-Aldrich), and supplemented with 0.2 mM BF.sub.3.Math.OEt.sub.2 2.0 h later. After the above solution was stirred at −78° C. for 3.0 h, the reaction was stopped with a small amount of methanol. The reaction solution was added dropwise to 2.0 L of methanol with rapid stirring to give a light yellow precipitate. The precipitate was washed with methanol, filtered and dried in an oven at 60° C. under vacuum for 6.0 h to give a light yellow solid powder, which was PBVE as shown in the proton NMR spectrum (
[0201] b. Preparation of dry hydrogen bromide gas (HBr); in a 100 mL two-neck flask, 5.0-30 mL of phosphorus tribromide (PBr.sub.3, Aladdin) was added dropwise to 10 mL of 48% aqueous solution of hydrogen bromide (HBr, Alfa Aesar). The resulting gas was allowed to sequentially pass through tetrachloromethane (CCl.sub.4), red phosphorus (P, Alfa Aesar) and calcium chloride (CaCl.sub.2) to give a dry HBr gas.
[0202] c. Preparation of isotactic polyvinyl alcohol (isotactic-PVA, i-PVA). 0.5 g of PBVE was dissolved in 15 mL of dry toluene under argon atmosphere, and dry argon was continuously introduced to remove oxygen from the resulting solution. The dry HBr gas prepared in the step b was allowed to pass into the above oxygen-free toluene solution of PBVE at 0° C. After about 5.0 min, a light yellow precipitate formed, and the introduction of dry HBr gas was continued until no precipitate formed. The above reaction solution was poured into 200 mL of methanol solution of ammonia (2.0 M).The resulting precipitate was washed with methanol, filtered, and dried in an oven at 60° C. under vacuum for 6.0 h to give a light yellow solid powder. The proton NMR spectrum (
(5) Verification of Ice Growth Inhibition Effect of Synthesized PVA
(5.1) Dynamic Light Scattering (DLS) Experiment
[0203] The grain size distributions of the two PVAs (a-PVA: the molecular weight of about 13-23 kDa, the diad syndiotacticity r of about 55% (Sigma-Aldrich); i-PVA: the molecular weight of about 14-26 kDa, the isotacticity m of about 84%) in an aqueous solution at 25° C. were measured by a DLS experiment, and an experimental instrument was a Nano ZS (Malvern Instruments) with a thermostatic chamber and a 4 mW He-Ne laser (λ=632.8 nm), wherein the scattering angle is 173° . Firstly, aqueous solutions of the a-PVA and the i-PVA at the concentrations of 1.0 mg.Math.mL.sup.−1, 4.0 mg.Math.mL.sup.−1, 10 mg.Math.mL.sup.−1 and 20 mg.Math.mL.sup.−1 were prepared; about 1.0 mL of each the PVA solution was added into a 12 mm disposable polystyrene cuvette for measurement.
[0204] The results of the DLS experiment show that when being at the same concentration, the a-PVA has a much smaller dispersion size in an aqueous solution than the i-PVA (
(5.2) Assay for Ice Recrystallization Inhibition (IRI) Activity
[0205] The IRI activity was assessed using “splat-freezing method”, wherein a sample was dissolved and dispersed into a DPBS solution, and 10-30 μL of the resulting solution was added dropwise onto the surface of a clean silicon disk pre-cooled at -60° C. at a height of no less than 1.0 m; the solution was slowly heated to -6° C. at a speed of 10° C. .Math.min.sup.−1 by using a hot-cold stage, and was annealed for 30 min at this temperature; the sizes of ice crystals were observed and recorded by using a polarizing microscope and a high-speed camera. The hot-cold stage was sealed to ensure that the internal humidity was about 50%. The procedure was repeated at least three times for each sample, and the sizes of ice crystals were counted using a Nano Measurer 1.2, with the error of the result being the standard deviation.
(5.3) Ice Topography (DIS) Observation and Thermal Hysteresis (TH) Measurement
[0206] DIS observation and TH measurement were performed by using a nanoliter osmometer. A capillary was first melt with the outer flame of a alcohol burner, and simultaneously stretched to produce a capillary with a very fine pore size, and the capillary was then linked to a microsyringe; an immersion oil with higher viscosity was injected into a disk with micron-sized holes, and an aqueous solution in which the material was dissolved was injected into the microholes by using a microsyringe; the droplet was quickly frozen by regulating the temperature, and then slowly heated to give a single crystal ice, the single crystal ice was slowly cooled at the precision of 0.01° C., and the DIS observation and TH test were performed by using a microscope provided with a high-speed camera.
[0207] The ability of the a-PVA (M.sub.W 13-23 kD) to inhibit the growth of ice crystals is far better than that of the i-PVA (M.sub.W 14-26 kD) with the corresponding molecular weight (
[0208] As can be seen from the results of the MD simulation and the actual verification experiment, the results are good in consistency. The ice growth inhibition performance of the ice growth inhibition material can be accurately predicted by MD simulation, and the molecular design of the ice growth inhibition material can be effectively achieved.
[0209] Compounds of formula (1) to formula (9) were designed by the same molecular design method, synthesized and studied for their ice growth inhibition effects.
Example 2
Synthesis of Compound of Formula (1)
[0210] (1) 2-chlorotrityl chloride resin was placed into a reaction tube, and added with DCM (20 mL.Math.g.sup.1).
[0211] The resulting mixture was shaken for 30 min. With the use of a sand-core funnel by suction, the solvent was removed. The residue was added with a three-fold molar excess of Fmoc-L-Pro-OH and an eight-fold molar excess of DIEA, and finally added with D1VIF to dissolve. The resulting mixture was shaken for 30 min. Methanol was used for end-capping for 30 min.
[0212] (2) The solvent DMF was removed. 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added, and the solvent was removed after 5 min; 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added again, and the piperidine solution was removed after 15 min. A small amount of resin was taken and washed with ethanol three times, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The color turned dark blue, which suggested a positive reaction.
[0213] (3) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), a two-fold excess of Fmoc-L-Thr(tBu)-OH that was dissolved in as small an amount of DMF as possible was added to a reaction tube; a two-fold excess of HBTU was added. Immediately thereafter, an eight-fold excess of DIEA was added and reacted for 30 min.
[0214] (4) After the solution was removed by suction, a small amount of resin was taken and washed with ethanol three times, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The colorless mixture suggested a negative reaction, that is, the reaction was complete.
[0215] (5) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), the solvent was removed. 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added, and the solvent was removed after 5 min; 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added again, and the piperidine solution was removed after 15 min. A small amount of resin was taken and washed with ethanol, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The color turned dark blue, which suggested a positive reaction.
[0216] (6) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DCM (15 mL.Math.g.sup.−1, twice), the resin was dried by suction.
[0217] (7) The product was cleavaged using a cleavaging liquid (15 mL.Math.g.sup.−1, TFA:water:EDT:Tis=95:1:2:2, v/v) for 90 min. The cleavaging fluid was blown to dryness with nitrogen, and then frozen to dryness to give a crude product of polypeptide.
[0218] (8) The polypeptide was purified and subjected to salt-conversion or desalting by HPLC. HPLC: tR=6.1 mins (purification column model: Kromasil 100-5C18, 4.6 mm*250 mm; gradient eluent: acetonitrile with 0.1% TFA and aqueous solution with 0.1% TFA, 0 mins-1:99, 20 mins-1:9). The purified solution was frozen to dryness to give a purified product L-Thr-L-Pro (indicated as TP). The yield was about 80%. The mass spectrum presents [M+H].sup.+ at 217.3.
Example 3
Synthesis of Compound of Formula (2)
[0219] (1) 2-chlorotrityl chloride resin was placed into a reaction tube, and added with DCM (20 mL.Math.g.sup.−1). The resulting mixture was shaken for 30 min. With the use of a sand-core funnel by suction, the solvent was removed. The residue was added with a three-fold molar excess of Fmoc-L-Thr(tBu)-OH and an eight-fold molar excess of DIEA, and finally added with DMF to dissolve. The resulting mixture was shaken for 30 min. Methanol was used for end-capping for 30 min.
[0220] (2) The solvent DMF was removed. 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added, and the solvent was removed after 5 min; 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added again, and the piperidine solution was removed after 15 min. A small amount of resin was taken and washed with ethanol three times, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The color turned dark blue, which suggested a positive reaction.
[0221] (3) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), a two-fold excess of Fmoc-Arg(Pbf)-OH that was dissolved in as small an amount of DMF as possible was added to a reaction tube; a two-fold excess of HBTU was added. Immediately thereafter, an eight-fold excess of DIEA was added and reacted for 30 min.
[0222] (4) After the solution was removed by suction, a small amount of resin was taken and washed with ethanol three times, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The colorless mixture suggested a negative reaction, that is, the reaction was complete.
[0223] (5) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), the solvent was removed. 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added, and the solvent was removed after 5 min; 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added again, and the piperidine solution was removed after 15 min. A small amount of resin was taken and washed with ethanol, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The color turned dark blue, which suggested a positive reaction.
[0224] (6) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DCM (15 mL.Math.g.sup.−1, twice), the resin was dried by suction.
[0225] (7) The product was cleavaged using a cleavaging liquid (15 mL.Math.g.sup.−1, TFA:water:EDT:Tis=95:1:2:2, v/v) for 90 min. The cleavaging fluid was blown to dryness with nitrogen, and then frozen to dryness to give a crude product of polypeptide.
[0226] (8) The polypeptide was purified and subjected to salt-conversion or desalting by HPLC. HPLC: tR=4.8 mins (purification column model: Kromasil 100-5C18, 4.6 mm*250 mm; gradient eluent: acetonitrile with 0.1% TFA and aqueous solution with 0.1% TFA, 0 mins-1:99, 20 mins-1:4). The purified solution was frozen to dryness to give a purified product L-Thr-L-Arg (TR). The yield was about 80%. The mass spectrum presents [M+H].sup.+ at 276.2.
Example 4
Synthesis of Compound of Formula (3)
[0227] (1) 2-chlorotrityl chloride resin was placed into a reaction tube, and added with DCM (20 mL.Math.g.sup.−1). The resulting mixture was shaken for 30 min. With the use of a sand-core funnel by suction, the solvent was removed. The residue was added with a three-fold molar excess of Fmoc-L-Thr(tBu)-OH and an eight-fold molar excess of DIEA, and finally added with DMF to dissolve. The resulting mixture was shaken for 30 min. Methanol was used for end-capping for 30 min.
[0228] (2) The solvent DMF was removed. 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added, and the solvent was removed after 5 min; 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added again, and the piperidine solution was removed after 15 min. A small amount of resin was taken and washed with ethanol three times, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The color turned dark blue, which suggested a positive reaction.
[0229] (3) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), a two-fold excess of Fmoc-Arg(Pbf)-OH that was dissolved in as small an amount of DMF as possible was added to a reaction tube; a two-fold excess of HBTU was added. Immediately thereafter, an eight-fold excess of DIEA was added and reacted for 30 min.
[0230] (4) After the solution was removed by suction, a small amount of resin was taken and washed with ethanol three times, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The colorless mixture suggested a negative reaction, that is, the reaction was complete.
[0231] (5) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), the solvent was removed. 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added, and the solvent was removed after 5 min; 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added again, and the piperidine solution was removed after 15 min. A small amount of resin was taken and washed with ethanol, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The color turned dark blue, which suggested a positive reaction.
[0232] (6) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), the resin was dried by suction.
[0233] (7) Steps (3) to (5) were repeated to link amino acid Fmoc-L-Thr(tBu)-OH. After the product obtained by the reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DCM (15 mL.Math.g.sup.−1, twice), the resin was dried by suction.
[0234] (8) The product was cleavaged using a cleavaging liquid (15 mL.Math.g.sup.−1, TFA:water:EDT:Tis=95:1:2:2, v/v) for 90 min. The cleavaging fluid was blown to dryness with nitrogen, and then frozen to dryness to give a crude product of polypeptide.
[0235] (9) The polypeptide was purified and subjected to salt-conversion or desalting by HPLC. HPLC: tR =3.9 mins (purification column model: Kromasil 100-5C18, 4.6 mm*250 mm; gradient eluent: acetonitrile with 0.1% TFA and aqueous solution with 0.1% TFA, 0 mins-1:99, 20 mins-1:4). The purified solution was frozen to dryness to give a purified product L-Thr-L-Arg-L-Thr (TRT). The yield was about 75%. The mass spectrum presents [M+H].sup.+ at 377.4.
Example 5
Synthesis of Compound of Formula (4)
[0236] (1) 2-chlorotrityl chloride resin was placed into a reaction tube, and added with DCM (20 mL.Math.g.sup.−1). The resulting mixture was shaken for 30 min. With the use of a sand-core funnel by suction, the solvent was removed. The residue was added with a three-fold molar excess of Fmoc-L-Thr(tBu)-OH and an eight-fold molar excess of DIEA, and finally added with DMF to dissolve. The resulting mixture was shaken for 30 min. Methanol was used for end-capping for 30 min.
[0237] (2) The solvent DMF was removed. 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added, and the solvent was removed after 5 min; 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added again, and the piperidine solution was removed after 15 min. A small amount of resin was taken and washed with ethanol three times, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The color turned dark blue, which suggested a positive reaction.
[0238] (3) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), a two-fold excess of Fmoc-L-Pro-OH that was dissolved in as small an amount of DMF as possible was added to a reaction tube; and a two-fold excess of HBTU was added. Immediately thereafter, an eight-fold excess of DIEA was added and reacted for 30 min.
[0239] (4) After the solution was removed by suction, a small amount of resin was taken and washed with ethanol three times, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The colorless mixture suggested a negative reaction, that is, the reaction was complete.
[0240] (5) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), the solvent was removed. 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added, and the solvent was removed after 5 min; 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added again, and the piperidine solution was removed after 15 min. A small amount of resin was taken and washed with ethanol, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The color turned dark blue, which suggested a positive reaction.
[0241] (6) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), the resin was dried by suction.
[0242] (7) Steps (3) to (5) were repeated to link amino acid Fmoc-L-Thr(tBu)-OH. After the product obtained by the reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DCM (15 mL.Math.g.sup.−1, twice), the resin was dried by suction.
[0243] (8) The product was cleavaged using a cleavaging liquid (15 mL.Math.g.sup.−1, TFA:water:EDT:Tis=95:1:2:2, v/v) for 90 min. The cleavaging fluid was blown to dryness with nitrogen, and then frozen to dryness to give a crude product of polypeptide.
[0244] (9) The polypeptide was purified and subjected to salt-conversion or desalting by HPLC. HPLC: tR=7.6 mins (purification column model: Kromasil 100-5C18, 4.6 mm*250 mm; gradient eluent: acetonitrile with 0.1% TFA and aqueous solution with 0.1% TFA, 0 mins-1:99, 20 mins-2:8). The purified solution was frozen to dryness to give a purified product L-Thr-L-Pro-L-Thr (TPT). The yield was about 70%. The mass spectrum presents [M+H].sup.− at 318.3.
Example 6
Synthesis of Compound of Formula (5)
[0245] (1) 2-chlorotrityl chloride resin was placed into a reaction tube, and added with DCM (20 mL.Math.g.sup.−1). The resulting mixture was shaken for 30 min. With the use of a sand-core funnel by suction, the solvent was removed. The residue was added with a three-fold molar excess of Fmoc-L-Thr(tBu)-OH and an eight-fold molar excess of DIEA, and finally added with DMF to dissolve. The resulting mixture was shaken for 30 min. Methanol was used for end-capping for 30 min.
[0246] (2) The solvent DMF was removed. 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added, and the solvent was removed after 5 min; 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added again, and the piperidine solution was removed after 15 min. A small amount of resin was taken and washed with ethanol three times, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The color turned dark blue, which suggested a positive reaction.
[0247] (3) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), a two-fold excess of Fmoc-L-Ala-OH that was dissolved in as small an amount of DMF as possible was added to a reaction tube; a two-fold excess of HBTU was added. Immediately thereafter, an eight-fold excess of DIEA was added and reacted for 30 min.
[0248] (4) After the solution was removed by suction, a small amount of resin was taken and washed with ethanol three times, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The colorless mixture suggested a negative reaction, that is, the reaction was complete.
[0249] (5) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), the solvent was removed. 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added, and the solvent was removed after 5 min; 20% piperidine/DMF solution (10 mL.Math.g.sup.−1) was added again, and the piperidine solution was removed after 15 min. A small amount of resin was taken and washed with ethanol, added with a ninhydrin reagent, and heated at 105-110° C. for 5 min. The color turned dark blue, which suggested a positive reaction.
[0250] (6) After the product obtained by the above reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DMF (15 mL.Math.g.sup.−1, twice), the resin was dried by suction.
[0251] (7) Steps (3) to (5) were repeated to link amino acid Fmoc-L-Ala-OH. After the product obtained by the reaction was sequentially washed with DMF (15 mL.Math.g.sup.−1, twice), methanol (15 mL.Math.g.sup.−1, twice) and DCM (15 mL.Math.g.sup.−1, twice), the resin was dried by suction.
[0252] (8) The product was cleavaged using a cleavaging liquid (15 mL.Math.g.sup.−1, TFA:water:EDT:Tis=95:1:2:2, v/v) for 90 min. The cleavaging fluid was blown to dryness with nitrogen, and then frozen to dryness to give a crude product of polypeptide.
[0253] (9) The polypeptide was purified and subjected to salt-conversion or desalting by HPLC. HPLC: tR=7.9 mins (purification column model: Kromasil 100-5C18, 4.6 mm*250 mm; gradient eluent: acetonitrile with 0.1% TFA and aqueous solution with 0.1% TFA, 0 mins-1:99, 20 mins-1:9). The purified solution was frozen to dryness to give a purified product L-Ala-L-Ala-L-Thr (AAT). The yield was about 70%. The mass spectrum presents [M-8H].sup.+ at 260.1.
Example 7
Synthesis of Compounds of Formula (6), Formula (7) and Formula (8)
Preparation of a Compound of Formula (6):
[0254] (1) GDL-L-Thr was prepared by using a solid-phase synthesis method.
[0255] (2) Purification by HPLC. HPLC: tR=3.4 mins (purification column type: SHIMADZU Intertsil ODS-SP (4.6 mm*250 mm*5 μM), gradient eluent: acetonitrile with 0.1% TFA and aqueous solution with 0.1% TFA, 0.01-20 mins-1:99, 20-30 mins-21:79, 30-40 mins-100:0, 40-50 mins-1:99); the yield was about 50%. The mass spectrum presents [M-H].sup.+ at 296.099.
[0256] The GDL-L-Thr prepared by using the solid-phase synthesis method has higher purity, and is more easily to separate. The experimental results show that the GDL-L-Thr prepared by using the solid-phase synthesis method has higher purity and good capability of inhibiting the growth of ice crystals (
[0257] Compounds of both formulas (7) and (8) can be obtained by using a solid-phase synthesis method.
Example 8
Synthesis of Compound of Formula (9)
[0258] (1) A DCM solution of dichlorodimethylisilane was poured into a synthesis tube for polypeptide, and after standing for 30 min the tube was air-dried for later use.
[0259] (2) 100 mg of resin was placed into the synthesis tube, 2 mL of DMF was added, and nitrogen was introduced. The resin was swollen for 10 min and filtered by suction under vacuum.
[0260] (3) 1 mL of 4-methylpiperidine/DMF solution was added for deprotection, and removed after 5 min. 1 mL of 4-methylpiperidine/DMF solution was added again, and removed after 15 min. The mixture was bubbled and filtered by suction under vacuum.
[0261] (4) The mixture was washed with DMF 5 times, bubbled and filtered by suction under vacuum.
[0262] (5) The mixture was sequentially added with 0.5 mL of 2 M bromoacetic acid/DMF solution and N,N-diisopropylcarbodiimide/DMF solution, bubbled for 20 min, filtered by suction under vacuum, and washed with DMF 3 times.
[0263] (6) The mixture was added with 1 mL of 1 M primary amine/DMF solution, bubbled for 30 min, washed with DMF, and washed with dichloromethane (×3).
[0264] (7) Steps (5) and (6) were repeated until the desired molecular weight was reached.
[0265] (8) The mixture was added with 4 mL of a cracking liquid, homogeneously mixed, blown to dryness with nitrogen, finally frozen to dryness, and purified to give the purified product.
[0266] In a peptoid, R is —CH.sub.3, —CH.sub.2CH.sub.3 and —CH.sub.2CH.sub.2COOH. The mass spectrum presents [M+H].sup.+ with R being —CH.sub.3 at 444.6, [M+H].sup.+ with R being —CH.sub.2CH.sub.3 at 528.8, and [M+H].sup.+ with R being —CH.sub.2CH.sub.2COOH at 792.1.
##STR00005##
[Ice Recrystallization Inhibition Experiment]
[0267] The IRI activity was assessed using “splat-freezing method”, wherein a sample was dissolved and dispersed into a DPBS solution, and 10-30 μL of the resultant solution was added dropwise onto the surface of a clean silicon disk precooled at −60° C. at a height of no less than 1.0 m; the solution was slowly heated to −6° C. at a speed of 10° C./min by using a hot-cold stage, and was annealed for 30 min at this temperature; the sizes of ice crystals were observed and recorded by using a polarizing microscope and a high-speed camera. The hot-cold stage was sealed to ensure that the internal humidity was about 50%. The procedure was repeated at least three times for each sample, and the sizes of ice crystals were counted using a Nano Measurer 1.2, with the error of the result being the standard deviation.
[0268] DIS observation and TH measurement were performed by using a nanoliter osmometer. A capillary was first melt with the outer flame of a alcohol burner, and simultaneously stretched to produce a capillary with a very fine pore size, and the capillary was then linked to a microsyringe; an immersion oil with higher viscosity was injected into a disk with micron-sized holes, and an aqueous solution in which the material was dissolved was injected into the microholes by using a microsyringe; the droplet was quickly frozen by regulating the temperature, and then slowly heated to give a single crystal ice, the single crystal ice was slowly cooled at the precision of 0.01° C., and the DIS observation and TH test were performed by using a microscope provided with a high-speed camera.
[0269] An IRI activity test was performed on 20 μL of a DPBS solution of the TR prepared in Example 3 by using “splat-freezing method”. The determined MLGS (%) relative to that of DPBS is shown in
[0270] The deionized aqueous solution of the TR prepared in Example 3 was taken for DIS observation using a nanoliter osmometer. It was found that the TR had a weak modification effect on the topography of ice crystals (supercooling degree of −0.1° C., −0.4 to 0.01° C.), as shown in
[0271] IRI activity tests were performed on 20 μL of DPBS solutions of the GDL-L-Thr, GDL-L-Ser and GDL-L-Val prepared in Example 7 by using “splat-freezing method”. The determined MLGS (%) relative to that of DPBS is shown in
[0272] The deionized aqueous solution of the GDL-L-Thr prepared in Example 7 was taken for DIS observation using a nanoliter osmometer. It was found that the GDL-L-Thr had a weak modification effect on the topography of ice crystals (supercooling degree of −0.1° C., −0.4 to 0.01° C.), as shown in
[0273] IRI activity tests were performed on 20 μL of DPBS solutions of the compounds prepared in Example 8 by using “splat-freezing method”. The determined MLGS (%) relative to that of DPBS is shown in
[0274] The deionized aqueous solutions of the three peptoids prepared in Example 8 were taken for DIS observation using a nanoliter osmometer. It was found that the peptoids where R was —CH.sub.3 and —CH.sub.2CH.sub.3 had rather obvious modification effects on the topography of ice crystals, and the peptoids where R was —CH.sub.2CH.sub.2COOH had no modification effect on the topography of ice crystals (supercooling degree of −0.1° C., −0.4 to 0.01° C.). The topography obtained are shown in
[0275] The above results show that the prepared peptidic compounds have the activity to inhibit the growth of ice crystals and have modification effects on the topography of ice crystals, particularly the compound of formula (9) where R is —CH.sub.3 or —CH.sub.2CH.sub.3 has an excellent modification effect on the topography of ice crystals with no TH, and can achieve the effect of controlling the growth of ice crystals and be used in the cryopreservation solution.
[0276] B. Ice growth inhibition performance evaluation and screening of ice growth inhibition material The amount of the ice growth inhibition material adsorbed on an ice surface=(the mass of ice growth inhibition material adsorbed on ice surface m.sub.1/total mass of ice growth inhibition material in stock solution comprising ice growth inhibition material m.sub.2)×100%. In one embodiment, the ice adsorption experiment comprises the following steps:
[0277] S1, taking an ice growth inhibition material of the mass m.sub.2 to prepare an aqueous solution of the ice control material, and cooling to a supercooling temperature;
[0278] S2, placing a pre-cooled temperature-regulating rod into the aqueous solution to induce the growth of an ice layer on the surface of the temperature-regulating rod, continuously stirring the aqueous solution to enable the ice growth inhibition material to be gradually adsorbed onto the surface of the ice layer, and keeping the temperature of the aqueous solution and the temperature-regulating rod at a supercooling temperature; and
[0279] S3, determining the amount of the ice growth inhibition material absorbed on the ice surface.
[0280] The device shown in
Example 9
[0281] a-PVA: molecular weight of about 13-23 kDa, diad syndiotacticity r of about 55% (Sigma-Aldrich);
[0282] i-PVA: molecular weight of about 14-26 kDa, isotacticity m of about 84%.
[0283] (1) Measurement of spreading performance of two PVAs at ice-water interface
[0284] The amount of the PVAs adsorbed on an ice surface was determined by performing an ice adsorption experiment, and an experimental device is shown in
[0285] a. The a-PVA and the i-PVA were fluorescently labeled with FITC Isomer I.
[0286] b. The FITC-labeled aqueous solutions (40 mL) of the PVAs with different concentrations were placed in beakers, which were then placed in a recirculating cooling bath, and the temperatures of the solutions and the temperature-regulating rod were cooled to −0.1° C.
[0287] c. The temperature-regulating rod was inserted into liquid nitrogen for pre-cooling for 1.0 min before being inserted into the pre-cooled FITC-labeled aqueous solutions of the PVAs. Then, the temperature-regulating rod was rapidly inserted into the pre-cooled FITC-labeled aqueous solutions of the PVAs to induce an extremely thin ice layer on the surface of the temperature-regulating rod to further induce ice growth.
[0288] d. The aqueous FITC-labeled PVA solution was magnetically stirred continuously at a supercooling temperature of −0.1° C. for 1.0 h to allow the PVA to be gradually adsorbed onto the surface of the ice. The supercooling degree and the adsorption time were maintained unchanged during all adsorption experiments to ensure that the surface area of the resulting ice was almost maintained unchanged within an allowable error range.
[0289] e. The formed ice block was taken out from the solution, and the ice surface was rinsed with purified water to remove the solution attached to the surface. The ice block was melted.
[0290] f. The amount of the PVA absorbed on the ice surface was obtained by the mass ratio of the solute PVA in the ice block to the solute PVA in the original solution, the concentration of the PVA solution was determined by ultraviolet-visible spectrophotometry, and the volume was determined by a pipette and a measuring cylinder.
[0291] In ice adsorption experiments, the amounts of the a-PVA and the i-PVA absorbed with each concentration are shown in
[0292] The amount of the i-PVA adsorbed on the ice surface is higher than that of the a-PVA when the concentration of the i-PVA is more than or equal to 1.2 mL.Math.g.sup.−1, and the amount of the i-PVA absorbed on the ice surface is saturated when the concentration is 2.0 mL.Math.g.sup.−1 with the adsorption amount of 56.5%. Further, it is stated that the amount of the i-PVA required is much greater than that of the a-PVA when the amounts of the two PVAs absorbed on ice surfaces with the same size are saturated. That is, the a-PVA could more effectively cover the surface of ice.
[0293] (2) Assay for Ice Recrystallization Inhibition (IRI) Activity
[0294] The ice recrystallization inhibition (IRI) activity was assessed using “splat-freezing method”, wherein the two PVAs were separately dissolved and dispersed into DPBS solutions, and 10-30 μL of the resulting solution was added dropwise onto the surface of a clean silicon disk pre-cooled at −60° C. at a height of no less than 1.0 m; the solution was slowly heated to −6° C. at a speed of 10° C..Math.min.sup.−1 by using a hot-cold stage, and was annealed for 30 min at this temperature; the sizes of ice crystals were observed and recorded by using a polarizing microscope and a high-speed camera. The hot-cold stage was sealed to ensure that the internal humidity was about 50%. The procedure was repeated at least three times for each sample, and the size of the ice crystal was counted using a Nano Measurer 1.2, with the error of the result being the standard deviation.
[0295] The result is shown in
[0296] According to the results of Example 9, the i-PVA has a weaker affinity for water than the a-PVA. Therefore, the i-PVA tends to exist in an aggregated state in an aqueous solution and on an ice-water interface, while the a-PVA can be well spread in an aqueous solution and on an ice-water interface. The amount of the i-PVA required is much higher than that of the a-PVA when the amounts of the two PVAs absorbed on ice surfaces with the same size are saturated. Therefore, compared with the i-PVA, the a-PVA is a better ice growth inhibition material, playing a better role in inhibiting the growth of ice crystals at lower concentrations.
C. Formulation of Cryopreservation Solution and Preparation and Application Embodiments
Example 10
[0297] Preparation of Cryopreservation Solution Comprising PVA as Ice growth inhibition material
[0298] 1. Preparation of cryopreservation solutions: cryopreservation solutions were prepared according to the following formulations.
[0299] A cryopreservation solution A comprises the following components per 100 mL:
TABLE-US-00002 Substances Content PVA (g) 2.0 Ethylene glycol (mL) 10 DMSO (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0300] Solution preparation steps: 2.0 g of a PVA was dissolved in 25 mL of DPBS in a water bath at 80° C. by heating magnetic stirring, and pH was adjusted to 7.0 to give a solution 1 after the PVA was completely dissolved and cooled to the room temperature; 17 g (0.05 mol) of sucrose (the final concentration of the sucrose in the cryopreservation solution was 0.5 mol.Math.L.sup.−1) was ultrasonically dissolved in 25 mL of DPBS, and after the sucrose was completely dissolved, 10 mL of ethylene glycol and 10 mL of DMSO were added to give a solution 2; after returning to room temperature, the solution 1 and the solution 2 were homogeneously mixed, the pH was adjusted, the volume was made up to 80%, and 20 mL of serum was stored separately to be added when the cryopreservation to solution was used.
[0301] A cryopreservation solution B comprises the following components per 100 mL:
TABLE-US-00003 Substances Content L-Arg (g) 8.0 L-Thr (g) 4.0 PVA (g) 2.0 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0302] Solution preparation steps: 2.0 g of a PVA was dissolved in 20 mL of DPBS in a water bath at 80° C. by heating magnetic stirring, and pH was adjusted to 7.1 to give a solution 1; 8.0 g of L-Arg and 4.0 g of L-Thr were dissolved in 20 mL of DPBS, and the pH was adjusted to 7.1 to give a solution 2; 17 g (0.05 mol) of sucrose (the final concentration of the sucrose in the cryopreservation solution was 0.5 mol.Math.L.sup.−1) was ultrasonically dissolved in 20 mL of DPBS, and after the sucrose was completely dissolved, 10 mL of ethylene glycol was added to give a solution 3; after returning to room temperature, the solution 1, the solution 2 and the solution 3 were homogeneously mixed, the pH was adjusted, the volume was made up to 80%, and 20 mL of serum was added when the cryopreservation was used.
[0303] A cryopreservation solution C comprises the following components per 100 mL:
TABLE-US-00004 Substances Content PVA (g) 2.0 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0304] Solution preparation steps: 2.0 g of a PVA was dissolved in 25 mL of DPBS in a water bath at 80° C. by heating magnetic stirring, and pH was adjusted to 6.9 to give a solution 1; 17 g (0.05 mol) of sucrose (the final concentration of the sucrose in the cryopreservation solution was 0.5 mol.Math.L.sup.−1) was ultrasonically dissolved in 25 mL of DPBS, and after the sucrose was completely dissolved, 10 mL of ethylene glycol was added to give a solution 2; after returning to room temperature, the solution 1 and the solution 2 were homogeneously mixed, the pH was adjusted, the volume was made up to 80%, and 20 mL of serum was stored separately to be added when the cryopreservation solution was used.
[0305] A cryopreservation solution Cl comprises the following components per 100 mL:
TABLE-US-00005 Substances Content PVA (g) 1.0 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Serum (mL) 20 DPBS (ml) Balance
[0306] The solution preparation steps were the same as those of the cryopreservation solution C.
[0307] A cryopreservation solution D comprises the following components per 100 mL:
TABLE-US-00006 Substances Content PVA (g) 2.0 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 DPBS (mL) Balance
[0308] Solution preparation steps: 2.0 g of a PVA was dissolved in 30 mL of DPBS in a water bath at 80° C. by heating magnetic stirring, and pH was adjusted to 7.0 to give a solution 1; 17 g (0.05 mol) of sucrose (the final concentration of the sucrose in the cryopreservation solution was 0.5 mol.Math.L.sup.−1) was ultrasonically dissolved in 25 mL of DPBS, and after the sucrose was completely dissolved, 10 mL of ethylene glycol was added to give a solution 2; after returning to room temperature, the solution 1 and the solution 2 were homogeneously mixed, the pH was adjusted, and the volume was made up to 100 mL for later use.
[0309] A cryopreservation solution E comprises the following components per 100 mL:
TABLE-US-00007 Substances Content Poly-L-proline (g) 1.5 PVA (g) 2.0 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 DPBS (ml) Balance
[0310] Solution preparation steps: 2.0 g of a PVA was dissolved in 25 mL of DPBS in a water bath at 80° C. by heating magnetic stirring, and pH was adjusted to 7.0 to give a solution 1; 1.5 g of poly-L-proline (with the degree of polymerization of 15) was ultrasonically dissolved in another 20 mL of DPBS, and the pH was adjusted to 7.0 to give a solution 2; 17 g (0.05 mol) of sucrose (the final concentration of the sucrose in the cryopreservation solution was 0.5 mol.Math.L.sup.−1) was ultrasonically dissolved in 25 mL of DPBS, and after the sucrose was completely dissolved, 10 mL of ethylene glycol was added to give a solution 3; after returning to room temperature, the solution 1, the solution 2 and the solution 3 were homogeneously mixed, the pH was adjusted, and the volume was made up to 100 mL for later use.
[0311] The cryopreservation solution F comprises the following components per 100 mL:
TABLE-US-00008 Substances Content Poly-L-arginine (g, degree of polymerization 4.0 being 8) PVA (g) 1.0 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Serum (mL) 20 DPBS (ml) Balance
[0312] The solution preparation steps were the same as those of the cryopreservation solution E, and the serum was added when the cryopreservation solution was used.
[0313] 2. Preparation of freezing equilibration solutions: the freezing equilibration solutions were prepared according to the following formulations.
[0314] A freezing equilibration solution a: 7.5 mL of ethylene glycol and 7.5 mL of DMSO were added to 65 mL of DPBS, and mixed homogeneously, and 20 mL of serum was added when the freezing equilibration solution was used.
[0315] A freezing equilibration solution b: 7.5 mL of ethylene glycol was dissolved in 72.5 mL of DPBS, and mixed homogeneously, and 20 mL of serum was added when the freezing equilibration solution was used.
[0316] A freezing equilibration solution c: 2.0 g of a PVA was dissolved in 50 mL of DPBS in a water bath at 80° C. by heating magnetic stirring, pH was adjusted to 7.0 after the PVA was completely dissolved, 7.5 mL of ethylene glycol was added, and mixed homogeneously, the pH was adjusted, and the volume was made up to 100 mL for later use.
Comparative Example
[0317] A freezing equilibration solution a comprises, per 1 mL, 7.5% (v/v) of DMSO, 7.5% (v/v) of ethylene glycol, 20% (v/v) of fetal bovine serum and the balance of DPBS;
[0318] A cryopreservation solution 1# comprises, per 1 mL, 15% (v/v) of DMSO, 15% (v/v) of ethylene glycol, 20% (v/v) of fetal bovine serum, 0.5 M sucrose and the balance of DPBS.
[0319] A freezing equilibration solution 2# comprises, per 1 mL, 7.5% (v/v) of ethylene glycol, 20% (v/v) of fetal bovine serum and the balance of DPBS;
[0320] A cryopreservation solution 2# comprises, per 1 mL, 10% (v/v) of ethylene glycol, 20% (v/v) of fetal bovine serum, 0.5 M sucrose and the balance of DPBS.
[0321] A cryopreservation solution 3# comprises, per 1 mL, 10% (v/v) of DMSO, 15% (v/v) of fetal bovine serum and the balance of a-MEM (USA, Invitrogen, C1257150OBT).
[0322] The three formulations of the thawing solutions used in Example 10 and the comparative examples were as follows:
[0323] A thawing solution 1# comprises a thawing solution I (comprising sucrose at 1.0 mol.Math.L.sup.−1, 20% of serum and the balance of DPBS), a thawing solution II (comprising sucrose at 0.5 mol.Math.L.sup.−1, 20% of serum and the balance of DPBS), a thawing solution III (comprising sucrose at 0.25 mol.Math.L.sup.−1, 20% of serum and the balance of DPBS), and a thawing solution IV (comprising 20% of serum and the balance of DPBS).
[0324] A thawing solution 2# comprises a thawing solution I (comprising sucrose at 1.0 mol.Math.L.sup.−1, a PVA at 20 mg.Math.mL.sup.−1 and the balance of DPBS), a thawing solution II (comprising sucrose at 0.5 mol.Math.L.sup.−1, a PVA at 20 mg.Math.mL.sup.−1 and the balance of DPBS), a thawing solution III (comprising sucrose at 0.25 mol.Math.L.sup.−1, a PVA at 20 mg mL.sup.−1 and the balance of DPBS), and a thawing solution IV (comprising a PVA at 20 mg.Math.mL.sup.−1 and the balance of DPBS).
[0325] A thawing solution 3# comprises a thawing solution I (comprising sucrose at 1.0 mol.Math.L.sup.−1, a PVA at 20 mg.Math.mL.sup.−1, 10 mg.Math.mL.sup.−1 polyproline and the balance of DPBS), a thawing solution II (comprising sucrose at 0.5 mol.Math.L.sup.−1, a PVA at 20 mg.Math.mL.sup.−1, 5.0 mg.Math.mL.sup.−1 polyproline and the balance of DPBS), a thawing solution III (comprising sucrose at 0.25 mol.Math.L.sup.−1, a PVA at 20 mg.Math.mL.sup.−1, 2.5 mg.Math.mL.sup.−1 polyproline and the balance of DPBS), and a thawing solution IV (comprising a PVA at 20 mg.Math.mL.sup.−1 and the balance of DPBS).
Application Example 1
[0326] Oocytes and embryos were cryopreserved using the freezing equilibration solutions and the cryopreservation solutions of the above examples and comparative examples according to the schemes in Table 1 and Table 2, respectively. The survival rates in the embodiments of the present invention were the average survival rate of 3-12 repeated experiments.
1. Cryopreservation of Oocytes
[0327] Mouse oocytes were firstly equilibrated in a freezing equilibration solution for 5 min, and then put in the prepared cryopreservation solution for 1 min; the equilibrated oocytes in the cryopreservation solution were placed on a straw, then quickly put into liquid nitrogen (−196° C.), and continuously preserved after the carrying rod was sealed; at the time of thawing, the frozen oocytes were equilibrated in the thawing solution I at 37° C. for 5 min, and equilibrated in the thawing solutions II-IV in sequence for 3 min each; and after the thawed oocytes were cultured for 2 h, the number of the survived cells was observed, and the survival rates were calculated (see Table 1).
2. Cryopreservation of Embryos
[0328] Mouse embryos were firstly equilibrated in a freezing equilibration solution for 5 min, and then put into the cryopreservation solution prepared in accordance to the formulations of the above examples and comparative examples for 50 s; the equilibrated embryos in the cryopreservation solution were placed on a straw, then quickly put into liquid nitrogen (−196° C.) and continuously preserved after the carrying rod was sealed; at the time of thawing, the frozen embryos were equilibrated in the thawing solution I at 37° C. for 3 min, and then equilibrated in the thawing solutions II-IV in sequence for 3 min each; and after the thawed embryos were cultured for 2 h, the number of the survived embryos was observed, and the survival rates were calculated (see Table 2).
TABLE-US-00009 TABLE 1 Survival rates of cryopreserved mouse oocytes Equilibration Cryopreservation Thawing Total number of Survival rates No. solution solution solution frozen oocytes after 2 h Application a A Thawing 67 100.0% Embodiment 1 solution 1# Application b B Thawing 109 94.8% Embodiment 2 solution 1# Application b C Thawing 90 97.7% Embodiment 3 solution 1# Application c D Thawing 50 93.4% Embodiment 4 solution 1# Application c D Thawing 53 96.5% Embodiment 5 solution 2# Application c E Thawing 39 89.7% Embodiment 6 solution 1# Application c E Thawing 60 98.6% Embodiment 7 solution 3# Comparative a Freezing Thawing 146 95.0% Embodiment 1 solution 1# solution 1# Comparative Equilibration Freezing Thawing 96 81.9% Embodiment 2 solution 2# solution 2# solution 1# Comparative Equilibration Freezing Thawing 44 94.7% Embodiment 3 solution 2# solution 2# solution 2#
TABLE-US-00010 TABLE 2 Survival rates of cryopreserved mouse embryos Equilibration Cryopreservation Thawing Total number of Survival rates No. solution solution solution frozen embryos after 2 h Application c D Thawing 41 95.8% Embodiment 8 solution 1# Application c E Thawing 42 95.2% Embodiment 9 solution 1# Comparative a Freezing Thawing 38 94.3% Embodiment 4 solution 1# solution 1# Comparative Equilibration Freezing Thawing 39 82.4% Embodiment 5 solution 2# solution 2# solution 1#
[0329] The above data indicate that the survival rate of the cryopreservation solution can be no less than 90% and even 100%, and can reach or far exceed a cryopreservation thawing rate of a commercial cryopreservation solution comprising 15% DMSO and commonly available in clinical practice at present, and as can be seen from the comparison of Application Embodiment 1 (comprising 10% DMSO), Comparative Embodiment 2 (comprising 7.5% DMSO) and Comparative Embodiment 1 (namely commercial oocyte cryopreservation solution (comprising 15% DMSO)), the survival rate of oocytes is significantly improved by adding PVA; Application Embodiments 2-3 also show that the cryopreservation solution can have higher survival rates of oocytes or embryos by adding a small amount of DMSO or not adding DMSO, solving the problem that the DMSO concentration of commercial cryopreservation solutions commonly available in clinical practice is high and the damage to cells is large; moreover, Application Embodiments 5 and 7-9 show that higher survival rates of oocytes or embryos can be realized under the condition that DMSO and serum are not added in the freezing solutions, equilibration solutions and thawing solutions. The DMSO-free or serum-free cryopreservation solution solves the problems of short shelf life, introduction of parasitic biological pollutants and the like caused by serum comprised in the commercial cryopreservation solutions commonly available in clinical practice at present.
Application Example 2
Cryopreservation of Human Umbilical Cord Mesenchymal Stem Cells
[0330] Human umbilical cord mesenchymal stem cells were cryopreserved using the cryopreservation solutions of the above examples and comparative examples according to the scheme in Table 3.
[0331] Cryopreservation of human umbilical cord mesenchymal stem cells by microdroplet method: digesting human umbilical cord mesenchymal stem cells on a culture dish using 25% pancreatin for 2 min, putting the digested human umbilical cord mesenchymal stem cells into a culture solution (10% FBS+a-MEM culture medium) of the same volume, gently pipetting until the stem cells completely fall off, adding the cells into a 1.5 mL centrifuge tube for centrifuging for 5 min at 1000 rmp, discarding the supernatant (separating the cells from the culture medium), adding 10 μL of a freezing solution to the bottom of the centrifuge tube, gently pipetting to disperse stem cell clusters, placing the 10 μL of the freezing solution with the stem cells on a freezing slide, and cryopreserving the solution into liquid nitrogen (−196° C.). At the time of thawing, the straw with the cells and the freezing solution was placed directly in a culture medium at 37° C. for thawing. After thawing, cells were stained with trypan blue to observe the survival rates, and the number of cells was counted using an instrument JIMBIO-FIL, survival rate=number of live cells/total number of cells (see Table 3).
TABLE-US-00011 TABLE 3 Survival rates of cryopreserved human umbilical cord mesenchymal stem cells Cryopreservation Cryopreservation Survival No. solution method rates Application C1 Microdroplet method 72.2% Embodiment 10 Application D Microdroplet method 77.1% Embodiment 11 Application F Microdroplet method 92.4% Embodiment 12 Comparative Freezing solution Microdroplet method 63.9% Embodiment 6 1# Comparative Freezing solution Microdroplet method 76.6% Embodiment 7 3#
[0332] When the cryopreservation solution disclosed herein is used for cryopreservation of the human umbilical cord mesenchymal stem cells, the survival rates of the stem cells can reach 92.4% and 72.2%, respectively (in Application Embodiments 12 and 10) although no DMSO is added, and the survival rate can even reach 77.1% when no DMSO and serum is added, reaching the survival level of the existing freezing regent. This means that the freezing reagent can have the same effectiveness in freezing stem cells as a conventional freezing solution, a cryopreservation thawing rate of the reagent can reach or even be far higher than that of a commonly available cryopreservation solution comprising 10% DMSO (in Comparative Embodiment 7), and the PVA-based cryopreservation effect is remarkably superior to the PVA-free cryopreservation effect in Comparative Embodiment 6.
Application Example 3
Cryopreservation of Ovarian Organs and Ovarian Tissues
[0333] The ovarian organs of mice newly born within 3 days and the ovarian tissue slices of sexually mature mice were cryopreserved using the freezing equilibration solutions and cryopreservation solutions of the above examples and comparative examples according to the schemes in Table 4 and Table 5.
[0334] The intact ovarian organs or ovarian tissue slices were firstly equilibrated in an equilibration solution at room temperature for 25 min, and then put into the prepared cryopreservation solution for 15 min. Next, the intact ovarian organs or ovarian tissue slices were placed on a straw and put into liquid nitrogen for preservation. After being thawed, the intact ovarian organs or ovarian tissue slices were put into a culture solution (10% FBS+a-MEM) in an incubator at 37° C. in the presence of 5% CO.sub.2 for 2 h for further thawing. Next, the intact ovarian organs or ovarian tissue slices were fixed with 4% paraformaldehyde, embedded in paraffin, and subjected to HE staining, and then the morphology was observed. The results are shown in
TABLE-US-00012 TABLE 4 Ovarian organ cryopreservation scheme Equil- Cryo- ibration preservation Thawing No. solution solution solution Morphology Application c D Thawing FIG. 26 Embodiment 13 solution 2# Application b C1 Thawing FIG. 27 Embodiment 14 solution 1# Application b F Thawing FIG. 28 Embodiment 15 solution 1# Comparative a Freezing Thawing FIG. 25 Embodiment 8 solution 1# solution 1#
TABLE-US-00013 TABLE 5 Ovarian tissue cryopreservation scheme Cryo- Equilibration preservation Thawing No. solution solution solution Morphology Application c D Thawing FIG. 31 Embodiment 16 solution 2# Application b C1 Thawing FIG. 32 Embodiment 17 solution 1# Application b F Thawing FIG. 33 Embodiment 18 solution 1# Comparative a Freezing Thawing FIG. 30 Embodiment 9 solution 1# solution 1#
[0335] As can be seen from
[0336] As can be seen from
[0337] It can be seen that the cryopreservation solution prepared with the biomimetic PVA-based ice growth inhibition material as a main component disclosed herein has a good inhibition effect on the growth of ice crystals, can be used with DMSO being reduced in the preservation system or even without DMSO, maintain good biocompatibility, and can be simultaneously applied to cryopreservation of oocytes, embryos, stem cells, reproductive organs and tissues where high cell survival rates and good biological activity can be achieved.
Example 11
Preparation of Cryopreservation Solution Comprising Amino Acid as Ice Growth Inhibition Material
[0338] A cryopreservation solution G comprises the following components per 100 mL:
TABLE-US-00014 Substances Content L-Arg (g) 16.0 L-Thr (g) 8.0 DMSO (mL) 10 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0339] Solution preparation steps (total volume: 100 mL): 16 g of L-Arg and 8 g of L-Thr were dissolved in 25 mL of DPBS, and pH was adjusted to 6.9 to give a solution 1; 17 g (0.05 mol) of sucrose (the final concentration of the sucrose in the cryopreservation solution was 0.5 mol.Math.L.sup.−1) was ultrasonically dissolved in 25 mL of DPBS, and after the sucrose was completely dissolved, 10 mL of ethylene glycol and 10 mL of DMSO were sequentially added to give a solution 2; after returning to room temperature, the solution 1 and the solution 2 were homogeneously mixed, the pH was adjusted to 6.9, the volume was made up to 80% with DPBS, and 20 mL of fetal bovine serum was stored separately to be added before the cryopreservation solution was used.
[0340] A cryopreservation solution H comprises the following components per 100 mL:
TABLE-US-00015 Substances Content Poly-L-proline (g, degree of polymerization 1.5 being 15) DMSO (mL) 10 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0341] Solution preparation steps: 1.5 g of poly-L-proline (with the degree of polymerization of 15) was ultrasonically dissolved in 25 mL of DPBS, and pH was adjusted to 6.8 to give a solution 1; 17 g (0.05 mol) of sucrose was ultrasonically dissolved in 25 mL of DPBS, and after the sucrose was completely dissolved, 10 mL of ethylene glycol and 10 mL of DMSO were sequentially added to give a solution 2; after returning to room temperature, the solution 1 and the solution 2 were homogeneously mixed, the pH was adjusted to 7.0, the volume was made up to 80% with DPBS, and 20 mL of serum was stored separately to be added before the cryopreservation solution was used.
[0342] A cryopreservation solution I comprises the following components per 100 mL:
TABLE-US-00016 Substances Content Poly-L-arginine (g, degree of polymerization 1.5 being 8) DMSO (mL) 10 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0343] Solution preparation steps (total volume: 100 mL): 1.5 g of poly-L-arginine (with the degree of polymerization of 8) was ultrasonically dissolved in 25 mL of DPBS, and pH was adjusted to 7.0 to give a solution 1; 17 g (0.05 mol) of sucrose was ultrasonically dissolved in 20 mL of DPBS, and after the sucrose was completely dissolved, 10 mL of ethylene glycol and 10 mL of DMSO were sequentially added to give a solution 2; after returning to room temperature, the solution 1 and the solution 2 were homogeneously mixed, the pH was adjusted to 7.0, the volume was made up to 80% with DPBS, and 20 mL of serum was stored separately to be added before the cryopreservation solution was used.
[0344] A cryopreservation solution J comprises the following components per 100 mL:
TABLE-US-00017 Substances Content Poly-L-arginine (g, degree of polymerization 4.0 being 8) DMSO (mL) 7.5 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0345] The solution preparation steps were the same as those of the cryopreservation solution I.
[0346] A cryopreservation solution K comprises the following components per 100 mL:
TABLE-US-00018 Substances Content Poly-L-proline (g, degree 4.0 of polymerization being 8) DMSO (mL) 7.5 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0347] The solution preparation steps were the same as those of the cryopreservation solution I.
[0348] A cryopreservation solution L comprises the following components per 100 mL:
TABLE-US-00019 Substances Content L-Arg (g) 16.0 L-Thr (g) 8.0 DMSO (mL) 7.5 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0349] The solution preparation steps were the same as those of the cryopreservation solution G.
[0350] Preparation of freezing equilibration solutions: the freezing equilibration solutions were prepared according to the following formulations.
[0351] A freezing equilibration solution a: 7.5 mL of ethylene glycol and 7.5 mL of DMSO were added to 65 mL of DPBS, and mixed homogeneously, and 20 mL of serum was added when the freezing equilibration solution was used.
[0352] A freezing equilibration solution b: 7.5 mL of ethylene glycol was added to 72.5 mL of DPBS, and mixed homogeneously, and 20 mL of serum was added when the freezing equilibration solution was used.
Comparative Example 2
[0353] A freezing equilibration solution a comprises, per 1 mL, 7.5% (v/v) of DMSO, 7.5% (v/v) of ethylene glycol, 20% (v/v) of fetal bovine serum and the balance of DPBS;
[0354] A cryopreservation solution 1# comprises, per 1 mL, 15% (v/v) of DMSO, 15% (v/v) of ethylene glycol, 20% (v/v) of fetal bovine serum, 0.5 M sucrose and the balance of DPBS.
[0355] A cryopreservation solution 3# comprises, per 1 mL, 10% (v/v) of DMSO, 15% (v/v) of fetal bovine serum and the balance of a-MEM (USA, Invitrogen, C1257150OBT).
[0356] The formulation of the thawing solutions used in Example 11 and Comparative Example 2 was as follows:
[0357] A thawing solution 1# comprises a thawing solution I (comprising sucrose at 1.0 mol.Math.L.sup.−1, 20% of serum and the balance of DPBS), a thawing solution II (comprising sucrose at 0.5 mol.Math.L.sup.−1, 20% of serum and the balance of DPBS), a thawing solution III (comprising sucrose at 0.25 mol.Math.L.sup.−1, 20% of serum and the balance of DPBS), and a thawing solution IV (comprising 20% of serum and the balance of DPBS).
Application Example 4
Cryopreservation of Oocytes and Embryos
[0358] Oocytes and embryos were cryopreserved using the freezing equilibration solutions and cryopreservation solutions of Example 11 and Comparative Example 2 according to the schemes in Table 6 and Table 7. The freezing and thawing methods were the same as those in Application Example 1.
TABLE-US-00020 TABLE 6 Survival rates of cryopreserved mouse oocytes Equilibration Cryopreservation Thawing Total number of Survival rates No. solution solution solution frozen oocytes after 2 h Application a G Thawing 67 98.5% Embodiment 19 solution 1# Application a H Thawing 109 96.3% Embodiment 20 solution 1# Application a I Thawing 67 95.5% Embodiment 21 solution 1# Comparative a Freezing solution Thawing 146 95.0% Embodiment 10 1# solution 1#
TABLE-US-00021 TABLE 7 Survival rates of cryopreserved mouse embryos Equilibration Cryopreservation Thawing Total number of Survival rates No. solution solution solution frozen embryos after 2 h Application a J Thawing 25 100.00% Embodiment 22 solution 1# Comparative a Freezing Thawing 38 94.30% Embodiment 11 solution 1# solution 1#
[0359] As can be seen from the data in Tables 6 and 7, when the cryopreservation solution disclosed herein is used for cryopreservation of oocytes and embryos after the amount of DMSO and EG is reduced, the survival rate of the oocytes can reach no less than 95%, the survival rate of the embryos can reach 100%, a cryopreservation thawing rate of the cryopreservation solution disclosed herein can reach or even be far higher than that of a commercial cryopreservation solution comprising 15% DMSO and commonly available in clinical practice at present (in Comparative Embodiments 10-11), and the cryopreservation effect with the addition of the biomimetic amino acid ice growth inhibition material is remarkably superior to the cryopreservation effect without the addition of the biomimetic amino acid ice growth inhibition material.
Application Example 5
Cryopreservation of Human Umbilical Cord Mesenchymal Stem Cells
[0360] Human umbilical cord mesenchymal stem cells were cryopreserved using the cryopreservation solutions of Example 11 and Comparative Example 2 according to the scheme in Table 8. Freezing and thawing methods are seen from Application Example 2.
TABLE-US-00022 TABLE 8 Survival rates of cryopreserved human umbilical cord mesenchymal stem cells Cryopreservation Cryopreservation No. solution method Survival rates Application J Microdroplet 81.2% Embodiment 23 method Application K Microdroplet 82.6% Embodiment 24 method Application L Microdroplet 80.5% Embodiment 25 method Comparative Freezing solution 1# Microdroplet 63.9% Embodiment 12 method Comparative Freezing solution 3# Microdroplet 76.6% Embodiment 13 method
[0361] When the cryopreservation solution disclosed herein is used for cryopreservation of human umbilical cord mesenchymal stem cells, the survival rate of the stem cells can reach no less than 80% by adding only a small amount of DMSO (7.5%) or even not adding DMSO (for example, in Application Embodiments 23-25). This means that the freezing reagent can not only have the same effectiveness in freezing stem cells as a conventional cryopreservation solution, but also has a cryopreservation thawing rate even far higher than that of a commonly available cryopreservation solution comprising 10% DMSO (in Comparative Embodiment 13), and the cryopreservation effect with the addition of the biomimetic amino acid ice growth inhibition material is remarkably superior to the cryopreservation effect without the addition of the biomimetic amino acid ice growth inhibition material (in Comparative Embodiments 14 and 15).
Application Example 6
Cryopreservation of Ovarian Organs and Ovarian Tissues
[0362] The ovarian organs of mice newly born within 3 days and the ovarian tissue slices of sexually mature mice were cryopreserved using the freezing equilibration solutions and cryopreservation solutions of Example 11 and Comparative Example 2 according to the schemes in Table 9 and Table 10. Methods for freezing and thawing ovarian organs and ovarian tissues of sexually mature mice are seen from Application Example 3.
TABLE-US-00023 TABLE 9 Ovarian organ cryopreservation scheme Equilibration Cryopreservation No. solution solution Thawing solution Morphology Application a J Thawing solution 1# FIG. 34 Embodiment 26 Application a L Thawing solution 1# FIG. 35 Embodiment 27 Application a K Thawing solution 1# FIG. 36 Embodiment 28 Comparative a Freezing solution 1# Thawing solution 1# FIG. 25 Embodiment 14
TABLE-US-00024 TABLE 10 Ovarian tissue cryopreservation scheme Equilibration Cryopreservation No. solution solution Thawing solution Morphology Application a J Thawing solution 1# FIG. 37 Embodiment 29 Application a L Thawing solution 1# FIG. 38 Embodiment 30 Application a K Thawing solution 1# FIG. 39 Embodiment 31 Comparative a Freezing solution 1# Thawing solution 1# FIG. 30 Embodiment 15
Example 11
Preparation of Cryopreservation Solution Comprising Peptidic Compound as Ice Growth Inhibition Material
[0363] A cryopreservation solution M comprises the following components per 100 mL:
TABLE-US-00025 Substances Content TR (g) 28 DMSO (mL) 7.5 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0364] Solution preparation steps (total volume: 100 mL): 28 g of TR was ultrasonically dissolved in 25 mL of DPBS, and pH was adjusted to 7.0 to give a solution 1; 0.05 mol of sucrose was ultrasonically dissolved in 25 mL of DPBS, and after the sucrose was completely dissolved, 10 mL of ethylene glycol and 7.5 mL of DMSO were sequentially added to give a solution 2; after returning to room temperature, the solution 1 and the solution 2 were homogeneously mixed, the pH was adjusted, the volume was made up to 80% with DPBS, and finally 20 mL of serum was added before the cryopreservation solution was used.
[0365] A cryopreservation solution N comprises the following components per 100 mL:
TABLE-US-00026 Substances Content TPT (g) 28 DMSO (mL) 7.5 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0366] Solution preparation steps (total volume: 100 mL): 28 g of TPT was ultrasonically dissolved in 25 mL of DPBS, and pH was adjusted to 7.0 to give a solution 1; 0.05 mol of sucrose was ultrasonically dissolved in 25 mL of DPBS, and after the sucrose was completely dissolved, 10 mL of ethylene glycol and 7.5 mL of DMSO were sequentially added to give a solution 2; after returning to room temperature, the solution 1 and the solution 2 were homogeneously mixed, the pH was adjusted, the volume was made up to 80% with DPBS, and finally 20 mL of serum was added before the cryopreservation solution was used.
[0367] A cryopreservation solution 0 comprises the following components per 100 mL:
TABLE-US-00027 Substances Content TR (g) 28 Ethylene glycol (mL) 10 Sucrose (mol .Math. L.sup.−1) 0.5 Fetal bovine serum (mL) 20 DPBS (mL) Balance
[0368] Solution preparation steps (total volume: 100 mL): 28 g of TR was ultrasonically dissolved in 25 mL of DPBS, and pH was adjusted to 7.0 to give a solution 1; 0.05 mol of sucrose was ultrasonically dissolved in 25 mL of DPBS, and after the sucrose was completely dissolved, 10 mL of ethylene glycol was added to give a solution 2; after returning to room temperature, the solution 1 and the solution 2 were homogeneously mixed, the pH was adjusted, the volume was made up to 80% with p DPBS, and finally 20 mL of serum was added before the cryopreservation solution was used. Preparation of freezing equilibration solutions: the freezing equilibration solutions were prepared according to the following formulations.
[0369] A freezing equilibration solution a: 7.5 mL of ethylene glycol and 7.5 mL of DMSO were added to 65 mL of DPBS, and mixed homogeneously, and 20 mL of serum was added when the freezing equilibration solution was used.
Comparative Example 3
[0370] A freezing equilibration solution a comprises, per 1 mL, 7.5% (v/v) of DMSO, 7.5% (v/v) of ethylene glycol, 20% (v/v) of fetal bovine serum and the balance of DPBS;
[0371] A cryopreservation solution 1# comprises, per 1 mL, 15% (v/v) of DMSO, 15% (v/v) of ethylene glycol, 20% (v/v) of fetal bovine serum, 0.5 M sucrose and the balance of DPBS.
[0372] A cryopreservation solution 3# comprises, per 1 mL, 10% (v/v) of DMSO, 15% (v/v) of fetal bovine serum and the balance of a-MEM (USA, Invitrogen, C1257150OBT).
[0373] The formulation of the thawing solutions used in Example 12 and Comparative Example 3 was as follows: A thawing solution 1# comprises a thawing solution I (comprising sucrose at 1.0 mol.Math.L.sup.−1, 20% of serum and the balance of DPBS), a thawing solution II (comprising sucrose at 0.5 mol.Math.L.sup.−1, 20% of serum and the balance of DPBS), a thawing solution III (comprising sucrose at 0.25 mol.Math.L.sup.−1, 20% of serum and the balance of DPBS), and a thawing solution IV (comprising 20% of serum and the balance of DPBS).
Application Example 7
Cryopreservation of Oocytes and Embryos
[0374] Oocytes and embryos were cryopreserved using the freezing equilibration solutions and cryopreservation solutions of Example 13 and Comparative Example 2 according to the schemes in Table 11 and Table 12. The freezing and thawing methods were the same as those in Application Example 1.
TABLE-US-00028 TABLE 11 Survival rates of cryopreserved mouse oocytes Total number Equilibration Freezing Thawing of frozen Survival rates No. solution solution solution oocytes after 2 h Application a M Thawing 93 96.2% Embodiment 32 solution 1# Application a N Thawing 48 90% Embodiment 33 solution 1# Comparative a Freezing Thawing 146 95% Embodiment 16 solution 1# solution 1#
TABLE-US-00029 TABLE 12 Survival rates of cryopreserved mouse embryos Equilibration Freezing Thawing Total number Survival rates No. solution solution solution of embryos after 2 h Application a M Thawing 41 95.9% Embodiment 34 solution 1# Comparative a Freezing Thawing 38 94.3% Embodiment 17 solution 1# solution 1#
[0375] The data in Tables 11 and 12 show that the polypeptides disclosed herein are used for cryopreservation of oocytes and embryos, and that the survival rates of oocytes and embryos of the existing commercial cryopreservation solution (DMSO content 15%) can be achieved by adding only a small amount of DMSO (7.5%), and the data of Application Embodiments 32 and 34 show that TR polypeptides have a more excellent cryopreservation effect on oocytes and embryos.
Application Example 8
Cryopreservation of Human Umbilical Cord Mesenchymal Stem Cells
[0376] Human umbilical cord mesenchymal stem cells were cryopreserved using the cryopreservation solutions of Example 12 and Comparative Example 3 according to the scheme in Table 13. Freezing and thawing methods are seen from Application Example 2.
TABLE-US-00030 TABLE 13 Survival rates of cryopreserved human umbilical cord mesenchymal stem cells Cryopreservation Cryopreservation No. solution method Survival rates Application M Microdroplet 87.8% Embodiment 35 method Application O Microdroplet 75.1% Embodiment 36 method Comparative Freezing solution 3# Microdroplet 76.6% Embodiment 18 method
[0377] According to the results in Table 13, the cryopreservation solution disclosed herein without adding DMSO or adding only a small amount of DMSO (7.5%) can have a cell survival rate equivalent to that of a cryopreservation solution comprising 10% DMSO in the prior art, so that the amount of DMSO is greatly reduced, the damage and toxicity of DMSO to cells are reduced, and the passage stability and cell activity of the frozen stem cells can be greatly improved.
Application Example 9
Cryopreservation of Ovarian Organs and Ovarian Tissues
[0378] The ovarian organs of mice newly born within 3 days and the ovarian tissue slices of sexually mature mice were cryopreserved using the freezing equilibration solutions and cryopreservation solutions of Example 12 and Comparative Example 3 according to the schemes in Table 14 and Table 15. Methods for freezing and thawing ovarian organs and ovarian tissues of sexually mature mice are seen from Application Example 3.
TABLE-US-00031 TABLE 14 Ovarian organ cryopreservation scheme Equilibration Cryopreservation No. solution solution Thawing solution Morphology Application a M Thawing solution 1# FIG. 40 Embodiment 37 Comparative a Freezing solution Thawing solution 1# FIG. 25 Embodiment 19 1#
TABLE-US-00032 TABLE 15 Ovarian tissue cryopreservation scheme Equilibration Cryopreservation No. solution solution Thawing solution Morphology Application a M Thawing solution 1# FIG. 41 Embodiment 38 Comparative a Freezing solution Thawing solution 1# FIG. 30 Embodiment 20 1#
[0379] As can be seen from
[0380] It can be seen that the cryopreservation solution prepared with the biomimetic peptide ice growth inhibition material as a main component disclosed herein can be simultaneously applied to cryopreservation of oocytes, embryos, stem cells, reproductive organs and tissues, where high cell survival rates and good biological activity can be achieved.
[0381] The examples of the present invention have been described above. However, the present invention is not limited to the above embodiments. Any modification, equivalent, improvement and the like made without departing from the spirit and principle of the present invention shall fall within the protection scope of the present invention.