Rosin-based small molecular weight hydrogelator and its application

Abstract

The present disclosure discloses a rosin-based small molecular weight hydrogelator and an application thereof, and belongs to the fields of supramolecular chemistry, surfactant science and chemical utilization of rosin. The rosin-based small molecular hydrogel of the present disclosure can gel water at a very low concentration, and the critical gelling concentration is only 0.176 wt %. On average, each gelling agent molecule can hold 13,889 water molecules, which exhibits extremely high gel efficiency and the formed small molecular hydrogel also exhibits extremely high stability. This small molecule hydrogel is derived from the natural product rosin and has a mild nature. It can be used in the fields of drug sustained-release, tissue engineering, daily chemicals, medicine and so on. At the same time, the rosin-based small molecular hydrogel 6-dehydroabietylamide amine oxide in the present disclosure can form a stable gel emulsion for most oils, and can be used in many fields such as food, medicine, daily chemicals, tissue engineering, environmental protection, and water pollution control.

Claims

1. A compound, wherein the compound is a 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide having formula (1): ##STR00005##

2. A method of preparing the compound according to claim 1, wherein the method is as follows: ##STR00006##

3. A supramolecular hydrogel comprising the compound according to claim 1, wherein the compound is a gelling factor for forming the supramolecular hydrogel.

4. The supramolecular hydrogel according to claim 3, wherein a concentration of the compound in the supramolecular hydrogel ranges from 3 mmol.Math.L.sup.−1to 1,000 mmol.Math.L.sup.−1.

5. A sustained-release material comprising the compound according to claim 1, and a sustained-release substance.

6. A pharmaceutical wound dressing comprising a hydrogel, wherein the hydrogel comprises the compound according to claim 1 and an inflammatory or anti-bacterial ingredient, wherein the compound is a gelling factor for forming the hydrogel.

7. A water-soil moisturizing agent comprising the compound according to claim 1.

8. A hydrogel mask comprising a hydrogel, wherein the hydrogel comprises the compound according to claim 1, wherein the compound is a gel skeleton for forming the hydrogel.

9. The hydrogel mask according to claim 8, further comprising one or more of collagen, hyaluronic acid, arbutin and nicotinamide injected into the hydrogel mask.

10. A cell culture scaffold prepared by using the compound according to claim 1, wherein the cell culture scaffold is prepared by the following steps: forming a hydrogel by using the compound as a gel skeleton and providing a three-dimensional environment for cell growth.

11. An O/W type gel emulsion prepared by using the compound according to claim 1, wherein a stabilizer of the O/W type gel emulsion is prepared from the compound.

12. The O/W type gel emulsion according to claim 11, wherein a concentration of the compound in the gel emulsion ranges from 0.22% to 80% of a mass of a continuous phase, and a volume fraction of a disperse phase ranges from 1% to 98%.

13. A method for oil transportation using the compound according to claim 1, wherein the method comprises adding the compound as a stabilizer to an oil to obtain a solid or semi-solid oil for transport.

14. A method for synthesizing a porous material by using the compound according to claim 1, wherein the method comprises the following steps: adding a crosslinking agent and an initiator to an aqueous phase; preparing an emulsion containing the compound upon heating; adding a reducing agent to the prepared emulsion; after stirring uniformly, transferring the emulsion to a mold, cooling down to form a gel emulsion and curing; and washing the cured monolith to remove the gel emulsion and then drying.

15. A functional ingredient delivery system based on the compound according to claim 1, wherein the functional ingredient delivery system comprises an O/W type gel emulsion prepared by using the compound, and the functional ingredient is embedded in the gel emulsion; and a functional factor includes: probiotics, flavor substances, nutrients or drugs.

Description

BRIEF DESCRIPTION OF FIGURES

(1) FIG. 1 is the molecular structure of 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide.

(2) FIG. 2 is the molecular structure of 2-dehydroabietylamide-N,N-dimethyl-ethylamine oxide.

(3) FIG. 3 is the molecular structure of 3-dehydroabietylamide-N,N-dimethyl-propylamine oxide.

(4) FIG. 4 is a hydrogen nuclear magnetic resonance spectrum of 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide.

(5) FIG. 5 is a photograph of the appearance of a gel formed by 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide (concentrations from left to right are 4 mmol.Math.L.sup.−1, 10 mmol.Math.L.sup.−1, 15 mmol.Math.L.sup.−1, 20 mmol.Math.L.sup.−1, and 25 mmol.Math.L.sup.−1, respectively).

(6) FIG. 6 is a dynamic shear diagram of a gel formed by 5 mmol.Math.L.sup.−1 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide (G is the storage modulus with a solid symbol; G″ is the loss modulus with a hollow symbol).

(7) FIG. 7 is a steady-state shear diagram of 5 mmol.Math.L.sup.−1 2-dehydroabietylamide-N,N-dimethyl-ethylamine oxide aqueous solution (solid symbol) and 3-dehydroabietylamide-N,N-dimethyl-propylamine oxide aqueous solution (hollow symbol).

(8) FIG. 8 is an in situ frozen transmission electron micrograph of a 5 mmol.Math.L.sup.−1 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide gel.

(9) FIG. 9 is a circular dichroism spectrum of a 5 mmol.Math.L.sup.−1 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide gel.

(10) FIG. 10 is a release curve of Rhodamine B embedded by 20 mmol.Math.L.sup.−1R-6-OA at 37° C.

(11) FIG. 11 is a laser confocal micrograph of L929 cells after incubation.

(12) FIG. 12 is a diagram showing the surface tension γ of the 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide as a function of the concentration C.

(13) FIG. 13 is a photograph of the appearance of a dodecane/hydrogel emulsion stabilized by 20 mmol.Math.L.sup.−1 6-dehydroabietylamide amine oxide at different oil-water ratios (the volume ratio of dodecane/water from left to right is 9:1, 8:2, 7:3, 6:4, 5:5, 4:6, 3:7, 2:8, 1:9).

(14) FIG. 14 is a dynamic shear diagram of a dodecane/water (V.sub.water:V.sub.oil=1:1) gel emulsion stabilized by 20 mmol.Math.L.sup.−1 6-dehydroabietylamide amine oxide (G is the storage modulus with a solid symbol; G″ is the loss modulus with a hollow symbol).

(15) FIG. 15 is a laser confocal micrograph of a dodecane/water (V.sub.water:V.sub.oil=8:2) gel emulsion stabilized by 20 mmol.Math.L.sup.−1 6-dehydroabietylamide amine oxide.

(16) FIG. 16 a laser confocal micrograph of a dodecane/water (V.sub.water:V.sub.oil=2:8) gel emulsion stabilized by 20 mmol.Math.L.sup.−1 6-dehydroabietylamide amine oxide.

DETAILED DESCRIPTION

(17) The synthetic route of 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide is as follows:

(18) ##STR00004##

EXAMPLE 1: SYNTHESIS OF COMPOUND 1

(19) The dehydroabietic acid solid (30 g, 0.1 mol) was added to a three-necked flask equipped with an exhaust gas absorption device and a reflux condenser, and a small amount of 4-dimethylaminopyridine (DMAP) was added as a catalyst. When the temperature was raised to 50° C., thionyl chloride (17.94 g, 0.15 mol) was slowly added dropwise. A large amount of acid gas was generated during this process, which was absorbed by the exhaust gas absorption device. After completion of the dropwise addition, the temperature was set to 72° C. and the reaction was continued for 3 h. After completion of the reaction, excess thionyl chloride was removed by rotary distillation under reduced pressure to obtain a crude Compound 1.

EXAMPLE 2: SYNTHESIS OF COMPOUND 2

(20) In a three-necked flask, 1,6-hexanediamine (58.1 g, 0.5 mol) and dichloromethane were added and stirred well. At a temperature of −20° C., a solution of dehydroabietyl chloride (0.1 mol) in dichloromethane was slowly added dropwise, and the reaction was continued for 3 h after completion of the dropwise addition. After that, the product was transferred to a 1,000 mL beaker, water was added to the mixture, and the mixture was extracted with dichloromethane. The obtained organic layer was washed with water for 5-6 times and then the organic layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure to obtain Compound 2 as a yellow viscous liquid.

EXAMPLE 3: SYNTHESIS OF COMPOUND 3

(21) Compound 2 was dissolved in ethanol, and an 88% formic acid (26.15 g, 0.5 mol) solution and a 30% formaldehyde (50.03 g, 0.5 mol) solution were slowly added dropwise at room temperature in sequence. After completion of the dropwise addition, the reaction was carried out at 80° C. for 8 h. After completion of the reaction, the product was adjusted to pH=11 with a 15% NaOH solution and extracted with diethyl ether. The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure to obtain Compound 3 as a yellow viscous liquid.

EXAMPLE 4: SYNTHESIS OF COMPOUND 4

(22) Compound 3 was dissolved in ethanol, and a small amount of citric acid and disodium edetate were added. When the temperature was raised to 55° C., 30% H.sub.2O.sub.2 (17 g, 0.15 mol) was slowly added dropwise, and after completion of the dropwise addition, the reaction was carried out at 80° C. for 5 h. After completion of the reaction, ethanol was removed by distillation under reduced pressure. The product was purified by silica gel column chromatography (eluent:ethyl acetate:methanol=4:1) to obtain Compound 4 as a white powdery solid after vacuum drying.

EXAMPLE 5: SYNTHESIS OF 2-dehydroabietylamide-N,N-dimethyl-ethylamine oxide and 3-dehydroabietylamide-N,N-dimethyl-propylamine oxide

(23) Compound 1 was reacted with N,N-dimethylethylenediamine and N,N-dimethylpropanediamine, respectively, and then subjected to H.sub.2O.sub.2 oxidation and column chromatography to obtain two comparative 2-dehydroabietylamide-N,N-dimethyl-ethylamine oxide and 3-dehydroabietylamide-N,N-dimethyl-propylamine oxide respectively. Both are white powdery solids after drying.

EXAMPLE 6: DETERMINATION OF MOLECULAR STRUCTURE AND PURITY OF 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide

(24) An appropriate amount of rosin-based small molecular weight hydrogelator 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide was weighed and dissolved in deuterated reagent DMSO. The .sup.1H NMR test was carried out at 25° C. using an Aduance III NMR spectrometer. The resonant frequency of .sup.1H is 400 MHz. It can be seen from the hydrogen nuclear magnetic resonance spectrum of 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide in FIG. 4 that chemical shift of each hydrogen was consistent with the target product 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide, indicating that the final product was obtained. At the same time, there are no impurity peaks at the spectrum, indicating a high purity of the product.

(25) 1H NMR (400 MHz, DMSO) δ 7.61 (t, 1H, N20-1H), 7.16 (d, 1H, C11-1H), 7.03-6.92 (d, 1H C14-1H), 6.84 (s, 1H, C12-1H), 3.17-2.97 (m, 4H, C26-2H, C21-2H), 2.95 (s, 6H, C27-3H, C28-3H), 2.85-2.64 (m, 3H, C8-2H, C15-1H), 2.26 (d, 1H, C4-1H), 2.04 (d, 1H, C6-1H), 1.77-1.57 (m, 6H, C25-2H, C22-2H, C2-1H, C7-1H), 1.40 (m, 5H, C3-2H, C7-1H, C2-1H, C4-1H), 1.26 (m, 4H, C23-2H, C24-2H), 1.16 (s, 3H, C18-3H), 1.14 (d, 9H, C16-3H, C17-3H, C19-3H).

EXAMPLE 7: DETERMINATION OF GEL BEHAVIOR

(26) To 1 mL of deionized water, 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide was added (concentrations were 4 mmol.Math.L.sup.−1, 10 mmol.Math.L.sup.−1, 15 mmol.Math.L.sup.−1, 20 mmol.Math.L.sup.−1, and 25 mmol.Math.L.sup.−1, respectively). The solution was heated to 40° C. to completely dissolve the 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide, and then allowed to stand at room temperature, and the solution state was investigated.

(27) It can be seen from the photograph of the appearance of a gel formed by 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide in FIG. 5 (concentrations from left to right were 4 mmol.Math.L.sup.−1, 10 mmol.Math.L.sup.−1, 15 mmol.Math.L.sup.−1, 20 mmol.Math.L.sup.−1, and 25 mmol.Math.L.sup.−1, respectively) that when the concentration of 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide was greater than 4 mmol.Math.L.sup.−1, the 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide can support its own weight without flowing after invertion, indicating the formed gel has excellent viscoelasticity.

(28) In a hydrogel formed by 4 mmol.Math.L.sup.−1 of 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide, the critical gelling concentration of the 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide was only 0.176%. Upon conversion, on average, each gelling agent molecule can immobilize 13,889 water molecules, showing extremely high gelling efficiency.

EXAMPLE 8: VISCOELASTICITY INVESTIGATION OF HYDROGELS FORMED BY 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide

(29) The gel with a 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide concentration of 5 mmol.Math.L.sup.−1 was first heated to 45° C. and then cooled to 25° C. After completely gelling, the samples were tested for rheological properties at 25° C. Prior to dynamic scanning, a stress scan was performed to determine the linear viscoelastic region of the sample, and the samples are investigated in a linear viscoelastic region. It can be seen from the dynamic shear diagram of the gel formed by 5 mmol.Math.L.sup.−1 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide in FIG. 6 that within the tested frequency range, the elastic modulus of the gel formed by 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide was always greater than the viscous modulus, indicating that the gel system shows excellent elasticity. Within the tested frequency range of 0.01-100 rad.Math.s.sup.−1, the corresponding elastic modulus of the gel was measured as 10.8 Pa-12.7 Pa, and the viscous modulus of the gel was measured as 0.5 Pa-1.85 Pa. It can be seen that the elastic modulus of the sample was always greater than the viscous modulus, exhibiting prominent elastic properties.

EXAMPLE 9: VISCOELASTIC MEASUREMENT OF COMPARATIVE 2-dehydroabietylamide-N,N-dimethyl-ethylamine oxide AND 3-dehydroabietylamide-N,N-dimethyl-propylamine oxide AQUEOUS SOLUTIONS

(30) It can be seen from the steady-state shear diagram of oth at 5 mmol.Math.L.sup.−1 in FIG. 7 that whether at high shear rates or low shear rates, the viscosity of the system was comparable to the viscosity of water, and always behaved as a Newtonian fluid. Thus, neither 2-dehydroabietylamide-N,N-dimethyl-ethylamine oxide nor 3-dehydroabietylamide-N,N-dimethyl-propylamine oxide could form a gel.

EXAMPLE 10: MEASUREMENT OF MICROSTRUCTURE OF THE GEL SYSTEM FORMED BY 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide

(31) Sample preparation was carried out using an environment controlled low temperature sample preparation device Cryoplunge TM3, and the ambient temperature was fixed at 25° C. The relative humidity in the device cavity was adjusted to over 90%, about 5 μL of the sample was pipetted onto the surface of the micro-grid, and the droplets on the surface of the micro-gate were absorbed by patting the sample with the filter paper on both sides of Cp3 to obtain a very thin liquid film. The sample was then quickly inserted into liquid ethane cooled liquid nitrogen. The frozen sample was transferred to a sample rod cooled with liquid nitrogen and transferred to a transmission electron microscope for observation at an operating voltage of 120 kV. It can be seen from the in situ frozen transmission electron micrograph of a hydrogel sample formed by 5 mmol.Math.L.sup.−1 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide in FIG. 8 that the microscopic morphology of the hydrogel was a relatively rigid nanofiber having a cross-sectional diameter of about 10 nm and a length of more than 2 μm.

(32) The 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide hydrogel also exhibited an extremely strong stability. The reason was that the 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide molecule formed a left-handed helical fiber structure having a diameter of about 10 nm by molecular self-assembly. The fibers were intertwined to form a three-dimensional network structure, and then the water molecules are fixed by capillary action and, surface tension, leading to the formation of a stable hydrogel.

EXAMPLE 11: MEASUREMENT OF A CIRCULAR DICHROISM SPECTRUM OF A GEL FORMED BY 5 MMOL.Math.L.SUP.−1 .6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide

(33) The measurement was carried out on a circular dichroism spectrometer model MOS-450. The signal was recorded at intervals of 0.1 nm within the wavelength range of 300-180 nm. Gel samples were measured using a 0.1 mm quartz sample cell. It can be seen from the circular dichroism spectrum of the 5 mmol.Math.L.sup.−1 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide gel in FIG. 9 that the gel sample exhibited a strong CD signal, exhibited a positive absorption peak in the wavelength range of 190-212 nm, and exhibited a negative absorption peak in the wavelength range of 212-300 nm, indicating that the nanofiber formed in the system was a chiral aggregate structure having a left-handed helix.

EXAMPLE 12: GEL SUSTAINED-RELEASE PERFORMANCE TEST

(34) Rhodamine B was embedded in a hydrogel formed by 20 mmol.Math.L.sup.−1 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide and in vitro release experiments were carried out in a constant temperature oscillating water bath at 37° C. The absorbance of the release solution was measured by an ultraviolet-visible spectrophotometer to obtain an in vitro release curve. It can be seen from FIG. 10 that the release rate of Rhodamine B was only 28% within 5 h, and the release rate of Rhodamine B was 76% in 40 h, after which Rhodamine B exhibited a slower release. It can be seen that the hydrogel formed by 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide had good sustained-release ability and can be used in the fields of drug sustained release and so on.

EXAMPLE 13: USE OF HYDROGEL FORMED BY 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide FOR CELL INCUBATION

(35) L929 cells were encapsulated in a 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide gel under sterile conditions for 3D cell incubation. The cell suspension was added into the 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide solution with a sol state, and a cell/hydrogel system was formed within 30 s, and further incubated at 37° C. for 15 min. Thereafter, 2 mL of RPMI-1640 medium containing 10% FBS fetal bovine serum and 1% penicillin/streptomycin was gently added to the incubation dish, and the cell/hydrogel system was incubated in a humidified atmosphere of 37° C. and 5% CO.sub.2. The medium was replaced after 1 h of incubation and then replaced every 12 h. After incubation for 24 h, 48 h and 96 h, the cell/hydrogel system was stained with FDA/PI and the cells were observed by a confocal laser scanning microscope. It can be seen from FIG. 11 that L929 cells had higher viability and proliferative ability in the gel due to excellent biocompatibility of the 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide hydrogel. It can be seen that 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide hydrogel can be used as a 3D cell incubation scaffold and had potential application in cell therapy and tissue regeneration.

EXAMPLE 14

(36) Determination of surface tension. A series of aqueous surfactant solutions having different concentrations were prepared, and the surface tension was measured by a ring method at 25° C., and the surface tension curve was plotted.

(37) It can be seen from the surface tension y of the 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide as a function of the concentration C in FIG. 12 that the surfactant 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide had a critical micelle concentration of 0.56 mmol.Math.L.sup.−1 and γ.sub.cmc of 35 mN.Math.m.sup.−1. It indicates that 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide has good surface activity and can be used to stabilize emulsion.

EXAMPLE 15: PREPARATION OF O/W TYPE GEL EMULSION

(38) An amount of 6-dehydroabietylamide amine oxide was added to a 22 mm (d)×52 mm (h) glass vial with a total volume of 10 mL. After adding a certain amount of deionized water, the vial was heated in a water bath at 50° C. until the 6-dehydroabietylamide amine oxide was completely dissolved to obtain a transparent solution. Different volumes of oil were added to the 6-dehydroabietylamide amine oxide solution (the volume ratios of 6-dehydroabietylamide amine oxide solution to oil were 1:9, 2:8, 3:7, 4:6, 5:5, 6:4, 7:3, 8:2, and 9:1, and total volume was 4 mL), then the mixture was emulsified at 11,000 r/min using an ultraturrax homogenizer (IKA T18 basic, S18N-10G head) for 2 min. The emulsion was allowed to stand and cool at a low temperature to form a white gel emulsion.

(39) It can be seen from the photograph of a dodecane/hydrogel emulsion stabilized by 20 mmol.Math.L.sup.−1 6-dehydroabietylamide amine oxide at different oil-water ratios in FIG. 13 that the volume fraction of the oil phase was in the range of 10% to 90%, a stable gel emulsion can be formed, and no phase separation occurs.

EXAMPLE 16

(40) The dynamic rheological behavior of the system was determined by a rheometer (Discovery DHR-2, TA). The cone (ETC) used in the test had a cone angle of 2° and a diameter of 40 mm. The distance between the cone and the plate was 48 μm and the temperature was 25° C. First, the elastic modulus (G′) and the viscous modulus (G″) of the sample as a function of stress (0.1-1000 Pa) were determined to ensure that the subsequent tests for each sample were in the linear viscoelastic region. The stress of 0.8 Pa was selected, the sample was scanned at various frequencies (0.1 to 100 rad/s), and the values of G′ and G″ as a function of frequency were recorded.

(41) It can be seen from the curve of the storage modulus G′and the loss modulus G″ of the gel formed by 20 mmol.Math.L.sup.−1 6-dehydroabietylamide amine oxide and the dodecane/water (V.sub.water:V.sub.oil=1:1) gel emulsion stabilized by 20 mmol.Math.L.sup.−1 6-dehydroabietylamide amine oxide as a function of shear frequency in FIG. 14 that within the frequency range of 0.01-100 rad.Math.s.sup.−1, the elastic modulus of the corresponding gel emulsion was 67 Pa-14 Pa, and the viscous modulus of the corresponding gel emulsion was 45 Pa-3 Pa. The elastic modulus of the dodecane/water gel emulsion stabilized by 6-dehydroabietylamide amine oxide was always greater than the viscous modulus, indicating the elastic behavior of the gel emulsions.

EXAMPLE 17

(42) The droplets of the gel emulsion were observed using a TCS SP8 laser confocal microscope from Leica, Germany. A gel emulsion was prepared by adding 1×10.sup.−3 mol.Math.L.sup.−1 rhodamine B as an indicator to an aqueous solution of a certain amount of 6-dehydroabietylamide amine oxide. It can be seen from the laser confocal scanning micrograph of a dodecane/water (V.sub.water:V.sub.oil=8:2) gel emulsion stabilized by 20 mmol.Math.L.sup.−1 6-dehydroabietylamide amine oxide in FIG. 15 that when the volume fraction of the disperse phase was less than 74%, the droplets of the gel emulsion were regularly spherical. It can be seen from the laser confocal micrograph of a dodecane/water (V.sub.water:V.sub.oil=2:8) gel emulsion stabilized by 20 mmol.Math.L.sup.−1 6-dehydroabietylamide amine oxide in FIG. 16 that when the volume fraction of the disperse phase was greater than 74%, the high density extrusion between the droplets caused the emulsion to lose fluidity, and thus the emulsion droplets were polyhedral. When the volume fraction of the dispersed phase was less than 74%, the 6-dehydroabiantylamide amine oxide self-assembled in the continuous phase forms a three-dimensional network structure, preventing the coalescence of the droplets and forming a gel emulsion.

EXAMPLE 18: APPLICATION IN OIL TRANSPORTATION

(43) 6-dehydroabiantylamide-N,N-dimethyl-hexylamine oxide as a stabilizer was added to the oil to obtain a solid or semi-solid oil, which reduces the occurrence of oil spillage in the storage container or oil tanks so as to facilitate transport.

(44) After transportation, external stimulation can be performed to demulsify the mixture as required.

(45) The external stimulus can be the addition of an external chemical, such as an alcohol including methanol or ethanol, which destroys the gel structure of the 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide in the continuous phase. At the same time, the addition of alcohol reduces the stability of the adsorption film formed by the 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide molecule at the oil-water interface and the water polarity, which leads to the demulsification of the emulsion.

(46) The external stimulus can also be heating. For example, when the gel emulsion was heated to above 40° C., the gel structure of the continuous phase was broken, so that the gel emulsion became a common emulsion. The heating can also increase the Brownian motion of the liquid droplets, causing flocculation and coalescence, which leads to the demulsification of the gel emulsion.

EXAMPLE 19: APPLICATION IN THE PREPARATION OF POROUS MATERIALS

(47) The surface hydrophilic porous material prepared by taking O/W type gel emulsion as a template have good biocompatibility and have potential application value in tissue engineering scaffolds.

(48) 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide was added to deionized water and heated for being completely dissolved. N,N′-methylenebisacrylamide as crosslinking agent and ammonium persulfate and 2-hydroxyethyl methacrylate as initiators were dissolved in the above 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide solution, after uniformly mixing, dodecane was added, and then the mixture was emulsified at 11,000 r/min using an ultraturrax homogenizer (IKA T18 basic, S18N-10G head) for 2 min to form an O/W emulsion. N,N,N,N-tetramethylethylenediamine as reducing agent was then added to the emulsion. After stirring at 11,000 r/min for 30 s, the emulsion was transferred to a mold (polyethylene container) and cooled to form a gel emulsion, which was incubated at room temperature for 1 h. The obtained solid was immersed in propanol for 24 h and dried under vacuum at 60° C. to obtain a polymer porous material.

(49) Since the oil-water volume ratio of the gel emulsion stabilized by 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide can be arbitrarily regulated, the porous material prepared by taking the gel emulsion stabilized by 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide as a template can be arbitrarily adjusted in pore size and distribution.

EXAMPLE 20: GEL EMULSION STABILITY TEST

(50) To the 0.22% solution of 6-dehydroabietylamide amine oxide, different volumes of oil were added (the volume ratios of 6-dehydroabietylamide amine oxide solution to oil were 0.2:9.8, 3:7, 5:5,7:3, and 9.9: 0.1, and total volume was 4 mL), and then the mixture was emulsified at 11,000 r/min using an ultraturrax homogenizer (IKA T18 basic, S18N-10G head) for 2 min. The emulsion was allowed to stand and cool at a low temperature to form a white gel emulsion.

(51) The prepared gel emulsion was placed in a 20° C. incubator, and the stability of the gel emulsion was observed. The results were shown in Table 1 below. When the concentration of 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide as stabilizer was 0.22% of the mass of the continuous phase, and the volume fraction of the disperse phase was in the range of 1%-98%, a gel emulsion was formed. After placing for one year, the gel emulsion did not undergo demulsification and showed high stability. The higher the stabilizer content, the more stable the gel emulsion formed. Therefore, when the concentration of 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide as stabilizer ranged from 0.22% to 80% of the mass of the continuous phase, and the volume fraction of the disperse phase ranged from 1% to 98%, the gel emulsion as formed showed a high stability.

(52) TABLE-US-00001 TABLE 1 Stability of the gel emulsion stabilized by 0.22% 6-dehydroabietylamide-N,N-dimethyl-hexylamine oxide Volume fraction Volume of the fraction of continuous the disperse phase (%) phase (%) Stability 0.2 9.8 No demulsification occurs after incubation for one year. 3 7 No demulsification occurs after incubation for one year. 5 5 No demulsification occurs after incubation for one year. 7 3 No demulsification occurs after incubation for one year. 9.9 0.1 No demulsification occurs after incubation for one year.