Formulation for stabilizing bio-therapeutics
11666655 · 2023-06-06
Assignee
Inventors
- Anurag Singh Rathore (New Delhi, IN)
- V. Haridas (New Delhi, IN)
- Rohit Bansal (New Delhi, IN)
- Soumili Chattopadhyay (New Delhi, IN)
- Sameer Dhawan (New Delhi, IN)
Cpc classification
A61K45/06
HUMAN NECESSITIES
C07K16/00
CHEMISTRY; METALLURGY
A61K47/26
HUMAN NECESSITIES
A61K9/0019
HUMAN NECESSITIES
C08L89/00
CHEMISTRY; METALLURGY
C08L77/04
CHEMISTRY; METALLURGY
C08L89/00
CHEMISTRY; METALLURGY
C08L77/04
CHEMISTRY; METALLURGY
A61K47/60
HUMAN NECESSITIES
International classification
A61K47/60
HUMAN NECESSITIES
A61K39/395
HUMAN NECESSITIES
Abstract
The present disclosure relates to a formulation including: a) a dendron of Formula I; b) at least one bio-therapeutic; c) at least one buffer; and d) at least one salt, wherein the bio-therapeutic to dendron molar ratio is in the range of 1:0.5-1:3. The dendron stabilizes the bio-therapeutic in the formulation at a temperature of up to 55° C. ##STR00001##
Claims
1. A formulation comprising: a) a dendron of Formula I, ##STR00094## wherein R is C.sub.2-16 alkynyl, wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all ##STR00095## groups of all repeating units are attached to another repeating unit until the penultimate repeating unit of every branch, and the ##STR00096## groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc); b) at least one bio-therapeutic; c) at least one buffer solution; and d) at least one salt, wherein the at least one bio-therapeutic is monoclonal antibodies, and the at least one bio-therapeutic to the dendron molar ratio is in the range of 1:0.5-1:3.
2. The formulation as claimed in claim 1, wherein the dendron stabilizes the at least one bio-therapeutic in the formulation at a temperature of up to 55° C.
3. The formulation as claimed in claim 1, wherein the buffer solution is selected from the group consisting of phosphate buffer, citrate buffer, acetate buffer, histidine buffer, succinate buffer, and glycine buffer.
4. The formulation as claimed in claim 3, wherein the buffer solution is phosphate buffer.
5. The formulation as claimed in claim 1, wherein the salt is selected from the group consisting of sodium chloride, potassium chloride, calcium chloride, potassium iodide, magnesium chloride, magnesium sulfate, sodium citrate, and sodium acetate.
6. The formulation as claimed in claim 5, wherein the salt is sodium chloride.
7. The formulation as claimed in claim 1, wherein the formulation has a pH in the range of 5.5-8.
8. The formulation as claimed in claim 1, wherein the dendron has structure as represented by Formula I: ##STR00097## wherein R is ethynyl, ‘n’ is in the range of 1-7, the branch growth follows a dendritic pattern; all ##STR00098## groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the ##STR00099## groups of the terminal repeating units of all branches are attached to hydrogen.
9. The formulation as claimed in claim 1, wherein the at least one bio-therapeutic is stabilized by dendron of Formula I and remain stable at high temperatures of up to 55° C. for 10 days.
10. A process for preparing the formulation as claimed in claim 1, comprising the steps of: (a) contacting the at least one buffer solution and the at least one salt with the at least one bio-therapeutic to obtain a mixture; (b) contacting the mixture from step (a) with the dendron of Formula I to obtain the formulation.
11. The process as claimed in claim 10, wherein i) step (a) further comprises at least contacting the at least one buffer solution, the at least one salt, and the at least one bio-therapeutic with at least one anti-bacterial agent selected from the group consisting of sodium azide, thymol, benzalkonium chloride, and glycerol; ii) step (b) is carried out by contacting the mixture from step (a) with the dendron of Formula I using gel filtration chromatography based buffer exchange; and iii) steps (a) and (b) are carried out at a temperature in the range of 20-30° C.
Description
BRIEF DESCRIPTION OF DRAWINGS
(1) The detailed description is described with reference to the accompanying figures. In the figures, the left-most digit(s) of a reference number identifies the figure in which the reference number first appears. The same numbers are used throughout the drawings to reference like features and components.
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DETAILED DESCRIPTION OF THE INVENTION
(13) Those skilled in the art will be aware that the present disclosure is subject to variations and modifications other than those specifically described. It is to be understood that the present disclosure includes all such variations and modifications. The disclosure also includes all such steps, features, compositions and compounds referred to or indicated in this specification, individually or collectively, and any and all combinations of any or more of such steps or features.
Definitions
(14) For convenience, before further description of the present disclosure, certain terms employed in the specification, and examples are collected here. These definitions should be read in the light of the remainder of the disclosure and understood as by a person of skill in the art. The terms used herein have the meanings recognized and known to those of skill in the art, however, for convenience and completeness, particular terms and their meanings are set forth below.
(15) The articles “a”, “an” and “the” are used to refer to one or to more than one (i.e., to at least one) of the grammatical object of the article.
(16) The terms “comprise” and “comprising” are used in the inclusive, open sense, meaning that additional elements may be included. Throughout this specification, unless the context requires otherwise the word “comprise”, and variations, such as “comprises” and “comprising”, will be understood to imply the inclusion of a stated element or step or group of element or steps but not the exclusion of any other element or step or group of element or steps.
(17) The term “including” is used to mean “including but not limited to”. “Including” and “including but not limited to” are used interchangeably.
(18) The term “dendron” refers to a repetitively branched molecule. The repeating unit of the dendron of the present invention is the amino acid residue lysine.
(19) The term “monoclonal antibodies” refers to antibodies that are made by identical immune cells that are all clones of a unique parent cell. Monoclonal antibodies include IgE monoclonal antibodies, IgG1 monoclonal antibodies, peroxidase-anti-peroxidase conjugated monoclonal antibodies, human chorionic gonadotropin monoclonal antibodies, and anti-rabies monoclonal antibodies.
(20) The term “cytokines” refers to a substance produced by a variety of cells including immune cells like macrophages, B lymphocytes, etc., which play an important role in cell signaling. Cytokines include chemokines, lymphokines, and tumor necrosis factors.
(21) The term “growth factors” refers to a substance, which is required for the stimulation of growth in living cells. Growth factors include hormones.
(22) The term “interferons” refers to type of cytokines, which are released by host cells in response to pathogens such as viruses, bacteria, and parasites. Interferons include type I, type II, and type III interferons.
(23) The term “interferons” refers to a group of cytokines that play an important part in the immune system. Interleukins include interleukins IL-1 to IL-17.
(24) The term “anticoagulants” refers to compounds that prevent blood clotting (coagulation). Anticoagulants include autoprothrombin IIA.
(25) The term “bone morphogenetic proteins” refers to one of the important growth factors which play a critical role in bone and cartilage formation. Bone morphogenetic proteins include bone morphogenetic proteins BMP-1 to BMP-15.
(26) The term “antigens” refers to toxins or foreign bodies eliciting immune response, though they can sometimes also be a part of host itself.
(27) The term “enzyme” refers to a substance produced by a living organism which acts as a catalyst to bring about a certain biochemical reaction. Enzymes include lipases, amylases, maltases, pepsins, proteases.
(28) The terms, monoclonal antibodies, cytokines, growth factors, hormones, interferons, interleukins, anticoagulants, bone morphogenetic proteins, antigens, and enzymes can be proteins or non-proteins, though majority of them are generally proteins. The ones contemplated by the present invention are the ones with protein structures.
(29) The term “anti-bacterial agent” refers to any substance that protects the protein from bacterial contamination. Anti-bacterial agents include, but are not limited to, sodium azide, thymol, benzalkonium chloride, and glycerol.
(30) In the structural formulae given herein and throughout the present disclosure, the following terms have the indicated meaning, unless specifically stated otherwise.
(31) The term “alkyl” refers to a monoradical branched or unbranched saturated hydrocarbon chain having from 1 to 16 carbon atoms. This term is exemplified by groups such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, t-butyl, n-hexyl, n-decyl, tetradecyl, and the like. By way of further example, a C.sub.1-C.sub.16 alkyl contains at least one but no more than 16 carbon atoms. A methyl group (i.e., CH.sub.3—) is an example of a C.sub.1 alkyl radical. A dodecyl group (i.e., CH.sub.3 (CH.sub.2).sub.11—) is an example of a C.sub.12 alkyl radical. The groups may be optionally substituted.
(32) The term “alkenyl” refers to a branched or unbranched hydrocarbon chain having from 2 to 16 carbon atoms, and having at least one carbon-carbon double bond. This term is exemplified by groups such as ethenyl, n-propenyl, n-butenyl, n-hexenyl, and the like. The groups may be optionally substituted.
(33) The term “alkynyl” refers to a branched or unbranched hydrocarbon chain having from 2 to 16 carbon atoms, and having at least one carbon-carbon triple bond. This term is exemplified by groups such as ethynyl, n-propynyl, n-butynyl, n-hexynyl, and the like. The groups may be optionally substituted.
(34) It will be understood that “substitution” or “substituted with” includes the implicit proviso that such substitution is in accordance with permitted valence of the substituted atom and the substituent, and that the substitution results in a stable compound, e.g., which does not spontaneously undergo transformation such as by rearrangement, cyclization, elimination, etc.
(35) As used herein, the term “substituted” is contemplated to include all permissible substituents of organic compounds. In a broad aspect, the permissible substituents include acyclic and cyclic, branched and unbranched, carbocyclic and heterocyclic, aromatic and nonaromatic substituents of organic compounds. Illustrative substituents include, for example, those described herein. The permissible substituents can be one or more and the same or different for appropriate organic compounds. For purposes of this invention, the heteroatoms such as nitrogen may have hydrogen substituents and/or any permissible substituents of organic compounds described herein which satisfy the valences of the heteroatoms.
(36) “Halo” or “Halogen”, alone or in combination with any other term means halogens such as chloro (Cl), fluoro (F), bromo (Br) and iodo (I).
(37) The term “aryl” refers to an aromatic carbocyclic group of 5 to 22 carbon atoms having a single ring or multiple rings, or multiple condensed (fused) rings.
(38) The term “alkoxy” refers to an alkyl group of 1 to 16 carbon atoms attached via an oxygen linkage to the rest of the molecule, which may be optionally substituted by one or more substituents. Preferred alkoxy groups, without limitation, include —OCH.sub.3, —OC.sub.2H.sub.5 and the like.
(39) The term “cycloalkyl” refers to non-aromatic mono or polycyclic ring system of about 3 to 12 carbon atoms, which may be optionally substituted by one or more substituent's. The polycyclic ring denotes hydrocarbon systems containing two or more ring systems with one or more ring carbon atoms in common, i.e., a Spiro, fused or bridged structures. Preferred cycloalkyl groups include, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclooctanyl, perhydronaphthyl, adamantyl, noradamantyl and norbornyl groups, bridged cyclic groups or spirobicyclic groups e.g. Spiro [4.4] non-2-yl and the like.
(40) The term “heteroaryl” refers to a heteroaromatic carbocyclic group of 1 to 20 carbon atoms with one to five heteroatoms selected from nitrogen, phosphorus, oxygen and sulfur, having a single ring (e.g. pyridine) or multiple rings (e.g. isoquinoline), or multiple condensed (fused) rings. Preferred heteroaryls include thiophene, pyrazole, thiazole, pyridine, and the like. The groups may be optionally substituted.
(41) The term “heterocyclyl” refers to a stable 1 to 20 membered ring radical, which consists of carbon atoms and from one to five heteroatoms selected from nitrogen, phosphorus, oxygen and sulfur. For purposes of this invention the heterocyclic ring radical may be monocyclic, bicyclic or tricyclic ring systems, and the nitrogen, phosphorus, carbon, oxygen or sulfur atoms in the heterocyclic ring radical may be optionally oxidized to various oxidation states. In addition, the nitrogen atom may be optionally quaternized; and the ring radical may be partially or fully saturated. Preferred heterocyclyl groups, without limitation, include azetidinyl, acridinyl, benzodioxolyl, benzodioxanyl, benzofuranyl, carbazolyl, cinnolinyl, dioxolanyl, indolizinyl, naphthyridinyl, perhydroazepinyl, phenazinyl, phenothiazinyl, phenoxazinyl, phthalazinyl, pyrazolyl, pyridyl, pteridinyl, purinyl, quinazolinyl, quinoxalinyl, quinolinyl, isoquinolinyl, tetrazolyl, imidazolyl, tetrahydroisoquinolinyl, piperidinyl, piperazinyl, homopiperazinyl, 2-oxoazepinyl, azepinyl, pyrrolyl, 4-piperidonyl, pyrrolidinyl, pyrazinyl, pyrimidinyl, pyridazinyl, oxazolyl, oxazolinyl, triazolyl, indanyl, isoxazolyl, isoxazolidinyl, thiazolyl, thiazolinyl, thiazolidinyl, isothiazolyl, quinuclidinyl, isothiazolidinyl, indolyl, isoindolyl, indolinyl, isoindolinyl, octahydroindolyl, octahydroisoindolyl, quinolyl, isoquinolyl, decahydroisoquinolyl, benzimidazolyl, thiadiazolyl, benzopyranyl, benzothiazolyl, benzooxazolyl, thienyl, morpholinyl, thiomorpholinyl, thiamorpholinyl sulfoxide, furyl, tetrahydrofuryl, tetrahydropyranyl, chromanyl and isochromanyl.
(42) The term “alkenyl” refers to hydrocarbon group containing 2-16 carbon atoms and containing at least one carbon-carbon double bond. Preferred alkenyl groups, without limitation, include ethenyl, propenyl, butenyl, and the like. The groups may be optionally substituted.
(43) The term “alkynyl” refers to hydrocarbon group containing 2-16 carbon atoms and containing at least one carbon-carbon triple bond. Preferred alkynyl groups, without limitation, include ethynyl, propynyl, butynyl, and the like. The groups may be optionally substituted.
(44) The compounds described herein may contain one or more chiral centers and/or double bonds and therefore, may exist as stereoisomers, such as double-bond isomers (i.e., geometric isomers), regioisomers, enantiomers or diastereomers. Accordingly, the chemical structures depicted herein encompass all possible enantiomers and stereoisomers of the illustrated or identified compounds including the stereoisomerically pure form (e.g., geometrically pure, enantiomerically pure or diastereomerically pure) and enantiomeric and stereoisomeric mixtures. Enantiomeric and stereoisomeric mixtures can be resolved into their component enantiomers or stereoisomers using separation techniques or chiral synthesis techniques well known to the person skilled in the art. The compounds may also exist in several tautomeric forms including the enol form, the keto form and mixtures thereof. Accordingly, the chemical structures depicted herein encompass all possible tautomeric forms of the illustrated or identified compounds. It is also understood that some isomeric form such as diastereomers, enantiomers and geometrical isomers can be separated by physical and/or chemical methods and by those skilled in the art. Pharmaceutically acceptable solvates may be hydrates or comprising of other solvents of crystallization such as alcohols, ether, and the like.
(45) As discussed above, preserving proteins at a higher temperature without thermal degradation is a much sought-after goal, given the value it will add to the global effort being made towards mitigating life-threatening diseases. The present disclosure provides a dendron-based formulation to stabilize proteins at higher temperatures.
(46) According to one embodiment, the present disclosure relates to a formulation comprising:
(47) a) a dendron of Formula I,
(48) ##STR00008##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(49) ##STR00009##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(50) ##STR00010##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one bio-therapeutic;
c) at least one buffer solution; and
d) at least one salt,
wherein the bio-therapeutic to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the bio-therapeutic in the formulation at a temperature of up to 55° C.
(51) According to one embodiment, the present disclosure relates to a formulation as described herein, wherein the bio-therapeutic is selected from the group consisting of monoclonal antibodies, cytokines, growth factors, hormones, interferons, interleukins, anticoagulants, bone morphogenetic proteins, antigens, and enzymes.
(52) According to one embodiment, the present disclosure relates to a formulation as described herein, wherein the monoclonal antibody is IgG1 monoclonal antibody.
(53) According to one embodiment, the present disclosure relates to a formulation as described herein, wherein the buffer solution is selected from the group consisting of phosphate buffer, citrate buffer, acetate buffer, histidine buffer, succinate buffer, and glycine buffer.
(54) According to another embodiment, the present disclosure relates to a formulation as described herein, wherein the salt is selected from the group consisting of sodium chloride, potassium chloride, calcium chloride, potassium iodide, magnesium chloride, magnesium sulfate, sodium citrate, and sodium acetate.
(55) According to yet another embodiment, the present disclosure relates to a formulation comprising:
(56) a) a dendron of Formula I,
(57) ##STR00011##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-10 alkyl, C.sub.5-22 aryl, C.sub.1-10 alkoxy, C.sub.1-10 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(58) ##STR00012##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(59) ##STR00013##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) at least one buffer solution; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(60) According to yet another embodiment, the present disclosure relates to a formulation comprising:
(61) a) a dendron of Formula I,
(62) ##STR00014##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of C.sub.1-16 straight chain aliphatic group, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(63) ##STR00015##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(64) ##STR00016##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one bio-therapeutic;
c) at least one buffer solution; and
d) at least one salt,
wherein the bio-therapeutic to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the bio-therapeutic in the formulation at a temperature of up to 55° C.
(65) According to yet another embodiment, the present disclosure relates to a formulation comprising:
(66) a) a dendron of Formula I,
(67) ##STR00017##
wherein R is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of C.sub.1-16 straight chain aliphatic group, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(68) ##STR00018##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(69) ##STR00019##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one bio-therapeutic;
c) at least one buffer solution; and
d) at least one salt,
wherein the bio-therapeutic to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the bio-therapeutic in the formulation at a temperature of up to 55° C.
(70) According to yet another embodiment, the present disclosure relates to a formulation comprising:
(71) a) a dendron of Formula I,
(72) ##STR00020##
wherein R is ethynyl,
‘n’ is in the range of 1-7, the branch growth follows a dendritic pattern; all
(73) ##STR00021##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(74) ##STR00022##
groups of the terminal repeating units of all branches are attached to hydrogen;
b) at least one bio-therapeutic;
c) at least one buffer solution; and
d) at least one salt,
wherein the bio-therapeutic to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the bio-therapeutic in the formulation at a temperature of up to 55° C.
(75) According to one embodiment, the present disclosure relates to a formulation comprising:
(76) a) a dendron of Formula I,
(77) ##STR00023##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(78) ##STR00024##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(79) ##STR00025##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) at least one buffer solution; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:2.5 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(80) According to one embodiment, the present disclosure relates to a formulation comprising:
(81) a) a dendron of Formula I,
(82) ##STR00026##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(83) ##STR00027##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(84) ##STR00028##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(85) According to another embodiment, the present disclosure relates to a formulation comprising:
(86) a) a dendron of Formula I,
(87) ##STR00029##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)N.sub.Rb.sub.c, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(88) ##STR00030##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(89) ##STR00031##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and
fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:2 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(90) According to another embodiment, the present disclosure relates to a formulation comprising:
(91) a) a dendron of Formula I,
(92) ##STR00032##
wherein R is selected from the group consisting of C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(93) ##STR00033##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(94) ##STR00034##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:1-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(95) According to yet another embodiment, the present disclosure relates to a formulation comprising:
(96) a) a dendron of Formula I,
(97) ##STR00035##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(98) ##STR00036##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(99) ##STR00037##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:1.5 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(100) According to one embodiment, the present disclosure relates to a formulation comprising:
(101) a) a dendron of Formula I,
(102) ##STR00038##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and L are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(103) ##STR00039##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(104) ##STR00040##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:1-1:2 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(105) According to one embodiment, the present disclosure relates to a formulation comprising:
(106) a) a dendron of Formula I,
(107) ##STR00041##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(108) ##STR00042##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(109) ##STR00043##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:2 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(110) According to another embodiment, the present disclosure relates to a formulation comprising:
(111) a) a dendron of Formula I,
(112) ##STR00044##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.1-16 alkoxy, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(113) ##STR00045##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(114) ##STR00046##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:1-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(115) According to yet another embodiment, the present disclosure relates to a formulation comprising:
(116) a) a dendron of Formula I,
(117) ##STR00047##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(118) ##STR00048##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(119) ##STR00049##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:2 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(120) According to yet another embodiment, the present disclosure relates to a formulation comprising:
(121) a) a dendron of Formula I,
(122) ##STR00050##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(123) ##STR00051##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(124) ##STR00052##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(125) According to one embodiment, the present disclosure relates to a formulation comprising:
(126) a) a dendron of Formula I,
(127) ##STR00053##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(128) ##STR00054##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(129) ##STR00055##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:2 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(130) According to another embodiment, the present disclosure relates to a formulation comprising:
(131) a) a dendron of Formula I,
(132) ##STR00056##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(133) ##STR00057##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(134) ##STR00058##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen and tert-butyloxycarbonyl (Boc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:1-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(135) According to yet another embodiment, the present disclosure relates to a formulation comprising:
(136) a) a dendron of Formula I,
(137) ##STR00059##
wherein R is selected from the group consisting of C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(138) ##STR00060##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(139) ##STR00061##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(140) According to one embodiment, the present disclosure relates to a formulation comprising:
(141) a) a dendron of Formula I,
(142) ##STR00062##
wherein R is selected from the group consisting of C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(143) ##STR00063##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(144) ##STR00064##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:1-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(145) According to another embodiment, the present disclosure relates to a formulation comprising:
(146) a) a dendron of Formula I,
(147) ##STR00065##
wherein R is selected from the group consisting of C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(148) ##STR00066##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(149) ##STR00067##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:2 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(150) According to yet another embodiment, the present disclosure relates to a formulation comprising:
(151) a) a dendron of Formula I,
(152) ##STR00068##
wherein R is selected from the group consisting of C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(153) ##STR00069##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(154) ##STR00070##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:1-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(155) According to one embodiment, the present disclosure relates to a formulation comprising:
(156) a) a dendron of Formula I,
(157) ##STR00071##
wherein R is selected from the group consisting of C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(158) ##STR00072##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(159) ##STR00073##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:2 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(160) According to another embodiment, the present disclosure relates to a formulation comprising:
(161) a) a dendron of Formula I,
(162) ##STR00074##
wherein R is selected from the group consisting of C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(163) ##STR00075##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(164) ##STR00076##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:1-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(165) According to yet another embodiment, the present disclosure relates to a formulation comprising:
(166) a) a dendron of Formula I,
(167) ##STR00077##
wherein R is selected from the group consisting of C.sub.2-16 alkynyl and —COOR.sub.a, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(168) ##STR00078##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(169) ##STR00079##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:1-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(170) According to one embodiment, the present disclosure relates to a formulation comprising:
(171) a) a dendron of Formula I,
(172) ##STR00080##
wherein R is ethynyl,
wherein ‘n’ is 1, and the
(173) ##STR00081##
groups are attached to hydrogen;
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(174) According to another embodiment, the present disclosure relates to a formulation comprising:
(175) a) a dendron of Formula I,
(176) ##STR00082##
wherein R is ethynyl,
wherein ‘n’ is 3; the branch growth follows a dendritic pattern; all
(177) ##STR00083##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(178) ##STR00084##
groups of the terminal repeating units of all branches are attached to hydrogen;
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(179) According to yet another embodiment, the present disclosure relates to a formulation comprising:
(180) a) a dendron of Formula I,
(181) ##STR00085##
wherein R is ethynyl,
wherein ‘n’ is 7; the branch growth follows a dendritic pattern; all
(182) ##STR00086##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(183) ##STR00087##
groups of the terminal repeating units of all branches are attached to hydrogen;
b) at least one monoclonal antibody;
c) phosphate buffer; and
d) sodium chloride,
wherein the monoclonal antibody to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the monoclonal antibody in the formulation at a temperature of up to 55° C.
(184) According to one embodiment, the present disclosure relates to a formulation as described herein, wherein the formulation has a pH in the range of 5.5-8.
(185) According to another embodiment, the present disclosure relates to a formulation wherein, the bio-therapeutics remain stable at high temperatures of up to 55° C. without considerable degradation, and can be used for curative purposes.
(186) According to another embodiment, the present disclosure relates to a process for the preparation of a formulation comprising:
(187) a) a dendron of Formula I,
(188) ##STR00088##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(189) ##STR00089##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(190) ##STR00090##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one bio-therapeutic;
c) at least one buffer solution; and
d) at least one salt,
wherein the bio-therapeutic to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the bio-therapeutic in the formulation at a temperature of up to 55° C.; the process comprising the steps of: (a) contacting at least one buffer solution and at least one salt solution with at least one bio-therapeutic to obtain a mixture; (b) contacting the mixture from step (a) with the dendron to obtain the formulation.
(191) According to another embodiment, the present disclosure relates to a process for the preparation of a formulation comprising:
(192) a) a dendron of Formula I,
(193) ##STR00091##
wherein R is selected from the group consisting of hydrogen, halogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 alkoxy, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl, C.sub.2-16 alkenyl, C.sub.2-16 alkynyl, —COOR.sub.a, —C(O)R.sub.b, —C(O)NR.sub.bR.sub.c, —NR.sub.dR.sub.e, —NR.sub.bC(O)R.sub.c, —OC(O)R.sub.b, wherein R.sub.a is selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.b and R.sub.c are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl; R.sub.d and R.sub.e are independently selected from the group consisting of hydrogen, C.sub.1-16 alkyl, C.sub.5-22 aryl, C.sub.1-16 haloalkyl, C.sub.3-12 cycloalkyl, C.sub.1-20 heteroaryl, C.sub.1-20 heterocyclyl,
wherein ‘n’ is in the range of 1-15; the branch growth follows a dendritic pattern; all
(194) ##STR00092##
groups of all repeating units are attached to another repeating unit till the penultimate repeating unit of every branch, and the
(195) ##STR00093##
groups of the terminal repeating units of all branches are attached to an atom or a functional group independently selected from the group consisting of hydrogen, tert-butyloxycarbonyl (Boc), and fluorenylmethyloxycarbonyl (Fmoc);
b) at least one bio-therapeutic;
c) at least one buffer solution; and
d) at least one salt,
wherein the bio-therapeutic to dendron molar ratio is in the range of 1:0.5-1:3 and the dendron stabilizes the bio-therapeutic in the formulation at a temperature of up to 55° C.; the process comprising the steps of: (a) contacting at least one buffer solution, at least one anti-bacterial agent selected from the group consisting of sodium azide, thymol, benzalkonium chloride, and glycerol, and at least one salt solution with at least one bio-therapeutic at a temperature in the range of 20-30° C., to obtain a mixture; (b) contacting the mixture from step (a) with the dendron by gel filtration chromatography based buffer exchange at a temperature in the range of 20-30° C., to obtain the formulation.
EXAMPLES
(196) The following examples provide the details about the synthesis of the dendrons and various analyses carried out on the formulation. It should be understood the following is representative only, and that the invention is not limited by the details set forth in these examples.
Example 1
(197) Synthesis of Dendrons and Related Intermediates
(198) The synthesis of dendrons was carried out in accordance with the following synthetic scheme (
(199) Scheme 1
(200) Materials and methods: All amino acids used were of L-configuration. Unless otherwise stated, all reagents were used without further purification. All solvents employed in the reactions were distilled or dried from appropriate drying agent prior to use. Amino acid L-Lysine, was purchased from SRL India. Reactions were monitored wherever possible by thin layer chromatography (TLC). Purification of compounds was done by silica gel column chromatography. Silica gel G (Merck) was used for TLC and column chromatography was done on silica gel (100-200 mesh) columns, which were generally made from slurry in hexane, hexane/ethyl acetate or dichloromethane. Analytical HPLC was carried out using Eclipse XDB-C18 column and acetonitrile/water as the solvent system. Detailed procedures have been described earlier..sup.4-6
a) General Procedure for the Boc-Protection
(201) To an ice cold and well-stirred solution of L-Lysine 0.0 mmol) in IN aq. NaOH, drop wise addition of Boc anhydride (2.2 mmol) was done over a period of 1 hr. The reaction mixture was stirred overnight, washed with hexane and acidified with saturated aq. solution of KHSO.sub.4 to make the pH=2. The N-protected amino acid was extracted with ethyl acetate. The organic layer was collected, dried over anhydrous Na.sub.2SO.sub.4, filtered and evaporated to obtain the N-protected amino acid in quantitative yields.
(202) b) General Procedure for the Peptide Coupling Reaction
(203) To an ice-cooled and well stirred solution of N-protected amino acid (1.0 mmoles) in dry dichloromethane, was added N-hydroxysuccinimide (NHS) (1.2 mmol), dicyclohexylcarbodiimide (DCC) (1.2 mmol) and stirred for 10 min. To this mixture was added an amine component (1.2 mmol) in dichloromethane and triethylamine (1.2 mmol). The reaction mixture was stirred overnight, filtered and the filtrate was washed with 0.2 N H.sub.2SO.sub.4, water and finally with saturated aqueous NaHCO.sub.3 solution. The organic layer was separated, dried over anhydrous Na.sub.2SO.sub.4, filtered and evaporated. Silica gel column chromatographic purification yielded the products in approximately 75-95% yields.
(204) c) General Procedure for the Boc-Deprotection
(205) To an ice-cooled solution of the Boc-protected compound (1 mmol) was added 25% solution of trifluroacetic acid TFA (40 mmol) in dry dichloromethane and stirred at room temperature for 3 hours. The reaction mixture was subjected to high vacuum, redissolved in ethylacetate/dichloromethane and washed with aqueous sodium carbonate. The organic layer was dried over anhydrous Na.sub.2SO.sub.4 and evaporated.
(206) All dendrons and related intermediates were characterized by .sup.1H NMR, .sup.13C NMR, IR and HRMS. Purity of the compounds was analyzed by analytical HPLC (Agilent Technologies 1200 series, Santa Clara, USA) equipped with Eclipse XDB-C18 reversed phase column using acetonitrile/water as the solvent system.
(207) d) Characterization Data
(208) First generation dendron A1 (Boc-protected intermediate): Synthesized using general procedure (a) wherein N-protected amino acid was Boc-Lys(Boc)-OH and amine component was propargyl amine.
(209) Yield: 94%; [α].sub.D: −1.8 (c=0.38, CHCl.sub.3)
(210) NMR (CDCl.sub.3, 300 MHz) δ 1.38-1.70 (s+m, 24H), 2.20 (t, J=2.4 Hz, 1H), 3.10 (m, 2H), 4.04 (m, 3H), 4.56 (br s, 1H), 5.03 (br d, 1H), 6.46 (br s, 1H); .sup.13C NMR
(211) (CDCl3, 75 MHz): δ 22.5, 28.2, 28.3, 28.9, 29.5, 32.0, 39.9, 54.1, 71.4, 79.0, 79.3, 80.0, 155.8, 156.1, 172.1; IR (KBr) 3333, 2977, 2935, 2866, 1687, 1524, 1453, 1376, 1249, 1171 cm.sup.−1; HRMS calculated for C.sub.19H.sub.33N.sub.3NaO.sub.5 m/z 406.2318, found m/z 406.2311.
(212) First generation dendron A2: Prepared using general procedure (b) from A1.
(213) Yield: 95%; [α].sub.D: +7.0 (c=0.1, MeOH)
(214) .sup.1H NMR (D.sub.2O, 300 MHz) δ 1.33-1.48 (m, 2H), 1.59-1.71 (m, 2H), 1.79-1.92 (m, 2H), 2.57 (s, 1H), 2.93 (t, 2H, J=7.2 Hz), 3.89-4.08 (m, 3H); .sup.13C NMR (D.sub.2O, 75 MHz): δ 21.2, 26.3, 28.9, 30.2, 39.0, 53.0, 72.2, 79.0, 169.4; IR (KBr): 3673, 3562, 3458, 3362, 2988, 2317, 2058, 1684, 1508, 1185, cm.sup.−1
(215) HRMS calculated for C.sub.9H.sub.18N.sub.3O m/z 184.1450, found m/z 184.1444.
(216) Second generation dendron B1: Prepared using general procedure (a) wherein N-protected amino acid was Boc-Lys(Boc)-OH and amine component was compound A2.
(217) Yield: 87%; [α].sub.D: −45.00 (c=0.39, CHCl.sub.3)
(218) .sup.1H NMR (CDCl.sub.3, 300 MHz) δ 1.37-1.85 (s+m, 54H), 2.25 (s, 1H), 3.10 (m, 6H), 4.02 (s, 2H), 4.09-4.45 (m, 3H), 4.70-5.00 (m, 2H), 5.60 (br s, 1H), 5.95 (br s, 1H), 7.14 (br d, 2H), 7.43 (br s, 1H); .sup.13C NMR (CDCl.sub.3, 75 MHz): δ 14.1, 22.1, 22.6, 22.7, 22.8, 28.4, 28.5, 29.1, 29.3, 29.5, 29.7, 30.6, 31.9, 32.6, 38.2, 39.9, 40.2, 53.1, 54.4, 71.6, 79.1, 79.5, 79.9, 80.2, 156.2, 171.5, 173.5; IR (KBr) 3340, 2932, 2862, 1691, 1651, 1527, 1450, 1372, 1249, 1169 cm.sup.−1; HRMS calculated for C.sub.41H.sub.73N.sub.7O.sub.11Na m/z 862.5266, found m/z 862.5262.
(219) Second generation dendron B2: Prepared using general procedure (b) from B1.
(220) Yield: 94%; [α].sub.D: +9.0 (c=0.1, MeOH)
(221) .sup.1H NMR (D.sub.2O, 300 MHz) δ 1.17-1.58 (m, 18H), 2.54 (s, 1H), 2.92 (br s, 3H), 3.09-3.41 (m, 3H), 3.56-4.25 (m, 5H); .sup.13C NMR (D.sub.2O, 75 MHz): δ 20.9, 21.2, 22.3, 26.3, 27.7, 28.7, 30.3, 38.9, 52.6, 53.0, 54.0, 71.8, 79.2, 110.4, 114.3, 118.1, 122.2, 162.5, 163.0, 169.4, 173.2; IR (KBr): 3711, 3647, 3441, 2924, 2334, 2037, 1682, 1201, 1001, cm.sup.−1
(222) HRMS calculated for C.sub.21H.sub.41N.sub.7O.sub.3 m/z 440.3349, found m/z 440.3342.
(223) Third generation dendron C1:
(224) Yield: 75%; [α].sub.D: +28.66 (c=0.1, MeOH).
(225) .sup.1H NMR (300 MHz, CDCl.sub.3): δ 1.15-2.05 (br m, 114H), 2.20 (s, 1H), 2.95-3.70 (br m, 14H), 3.90-4.60 (br m, 9H), 4.72-5.25 (br m, 4H), 5.52-6.18 (br m, 4H), 6.68-7.20 (br m, 2H), 7.32-7.90 (br m, 5H); .sup.13C NMR (75 MHz, CDCl.sub.3): δ 14.1, 22.7, 24.9, 25.6, 28.5, 29.7, 31.7, 31.9, 32.7, 33.9, 38.8, 39.9, 40.3, 53.0, 54.3, 71.4, 79.0, 79.9, 156.3, 172.6, 172.9, 173.6, 174.2; IR (KBr): 3325, 3082, 2976, 2934, 2861, 2247, 1693, 1649, 1527, 1452, 1392, 1367, 1249, 1171 cm.sup.−1. (HRMS): calculated for C.sub.85H.sub.153N.sub.15O.sub.23Na m/z 1775.1161, found m/z 1775.1158.
(226) Third generation dendron C2:
(227) Yield: 92%; [α].sub.D: +2.6 (c=0.1, MeOH)
(228) .sup.1H NMR (D.sub.2O, 300 MHz) δ 0.95-1.80 (m, 42H), 2.26 (s, 1H), 2.67 (br s, 8H), 2.87 (br s, 6H), 3.52-3.79 (m, 6H), 3.81-4.05 (m, 3H); .sup.13C NMR (D.sub.2O, 125 MHz): δ 6.9, 12.0, 16.2, 17.7, 21.3, 22.4, 26.3, 27.9, 28.7, 30.4, 38.9, 42.5, 52.7, 53.1, 54.3, 71.9, 79.4, 116.5, 118.9, 132.9, 163.2, 169.2, 173.2; IR (KBr) 3430, 2935, 1664, 1436, 1383, 1197, 1138 cm.sup.−1; HRMS calculated for C.sub.45H.sub.90N.sub.15O.sub.7 m/z 952.7148, found m/z 952.7139.
Example 2
(229) Preparation of the Formulation
(230) The protein used in the study (IgG1 monoclonal antibody) was stored at 4° C., pH 7.0, at a concentration of 30 mg/ml in a buffer containing 15 mM sodium phosphate, 150 mM NaCl, and 0.1% sodium azide. Sodium azide was used to avoid bacteria contamination.
(231) Protein was dialyzed into the required formulation by performing gel filtration chromatography-based buffer exchange using a Sephadex G-25 resin (GE Healthcare Biosciences, Pittsburgh, Pa., USA) packed into a Tricon™ column (100×10 mm). Concentration of the protein in the samples was measured by UV-VIS spectroscopy at 280 nm using a Spectra Max M2e Multimode Microplate Reader (Molecular Devices, Sunnyvale, Calif., USA) in congruence to the Lambert-Beer Law. Measurement of the concentration of the samples was performed in duplicate and concentration of the concerned buffer was subtracted. In each case, the sample concentration was measured after buffer exchange and the final concentration was adjusted to 5 mg/ml with the respective buffer.
Example 3
(232) Determination of Percentage of Monomer Loss in Formulation at High Temperature
(233) Various formulations were prepared as described above in Example 2. Dendrons of all three generations (A2, B2, and C2) were used for this purpose. Additionally, ratios of monoclonal antibodies (mAb) to dendrons were also varied. Thus, three formulations were prepared for each dendron (A2, B2, and C2), wherein the ratios of mAb to dendron were 1:1, 1:2, and 1:3. Commercially available mAb formulation containing polysorbate 80 (PS 80, a surfactant, purchased from Merck, India, and used as a 0.02% w/v solution) as an excipient was used for comparative purposes. These formulations were then incubated at a temperature of 55° C. for a period of 10 days. Aliquots were drawn at regular intervals and monomer loss was determined using size exclusion chromatography (SEC-HPLC). With progress of time, the monomer gets converted to aggregates and fragments, resulting in decrease in percentage of monomer and increase in the percentage of aggregates and fragments. These changes were measured by calculating peak area in the SEC chromatogram and a graph was plotted. Higher the percentage of monomer loss, lower was the stabilization provided. The results can be found in
Example 4
(234) Aggregation, Fragmentation, and Precipitation Studies
(235) Further studies were carried out to establish the versatility of the dendrons of instant invention in protecting the mAb from degradation by other modes. Proteins tend to aggregate in the solutions in which they are stored. When the aggregation reaches a certain level, these proteins precipitate out of the solution which is another form of protein degradation. Furthermore, these aggregates, depending upon their stability may fragment into smaller parts. Fragmentation may also take place directly without necessarily having to go through the aggregation stage. This fragmentation is another form of protein degradation and is highly undesirable. Experiments were thus undertaken to investigate the aggregation and fragmentation behavior of the mAb in the formulations of present invention. The formulations used for this purpose were same as those in Example 3. Akin to Example 3, formulation containing PS 80 was also used for comparative purpose. The detailed results are given in
Example 5
(236) Circular Dichroism (CD) Experiments to Study Secondary Structure
(237) With the intent of studying conformational stability of the mAb in formulations, Far-UV CD studies were carried out. Conformational stability is the ability of the protein to retain its secondary structure (alpha helix or beta sheet). mAbs studied in present invention are predominantly beta sheets. Thus, a higher beta sheet content implies a higher conformational stability.
Example 6
(238) Dynamic Light Scattering (DLS) Experiments
(239) DLS experiments were further carried out to collect additional data pertaining to the stability of the formulations.
(240) Advantages:
(241) 1) The disclosed formulation containing lysine-derived dendrons stabilizes monoclonal antibodies in a far efficient way compared to traditional formulations containing excipients like salts, sugars, amino acids, surfactants, and polymers. The use of amino-acid based dendrons for stabilization of proteins is hitherto unknown. 2) The formulation of present invention protects from degradation induced by both, physical and chemical means. 3) The formulation of the present invention provides unprecedented stabilization against heat induced protein degradation, in that the proteins (mAbs) remained stable in the formulation up to a temperature of 55° C. for 10 days.
(242) Although the subject matter has been described in considerable detail with reference to certain embodiments thereof, other embodiments are possible. As such, the spirit and scope of the invention should not be limited to the description of the embodiments contained herein.