METHOD FOR MAKING MODIFIED POLYVINYL ALCOHOL EMBOLIC MICROSPHERE

Abstract

The invention provides a making method of modified polyvinyl alcohol embolic microspheres. First, polyvinyl alcohol dimethyl sulfoxide solution is added to acryloyl chloride dichloromethane solution for reaction, then taurine solution is added to the above solution for further reaction, so that functional groups are introduced into the side chains of polyvinyl alcohol, then blank microspheres are prepared by suspension crosslinking method, and finally, drug-loaded modified polyvinyl alcohol embolic microspheres are prepared. The invention aims at improving the drug loading rate and drug loading speed of the microspheres. Through modification, the crystallinity of polyvinyl alcohol is weakened, the swelling in water is accelerated, and the application effect of the microspheres is improved.

Claims

1. A method for making modified polyvinyl alcohol embolic microspheres comprising: 1) putting polyvinyl alcohol in organic solvent A and stirring for preparing a polyvinyl alcohol solution; dissolving acryloyl chloride or butenoyl chloride in organic solvent B for preparing an acyl chloride solution; 2) adding an acid binding agent to the polyvinyl alcohol solution, dropping the acyl chloride solution into the polyvinyl alcohol solution, stirring for 3-5 hours at room temperature, then raising the temperature to 45-50? C., and stirring for additional 1-2 hours, cooling the reaction solution that results to room temperature, pouring the reaction solution into excess absolute ethanol for precipitating the polymer, then filtering, washing the polymer with absolute ethanol, drying the polymer to a constant weight in a drying oven, and obtaining allyl polyvinyl alcohol or butyryl polyvinyl alcohol; 3) weighing the dry allyl polyvinyl alcohol or butyryl polyvinyl alcohol and putting them in water to stir and dissolve them; then dissolving taurine in water to make a taurine solution, adding the taurine solution to the allyl polyvinyl alcohol solution or butyryl polyvinyl alcohol solution, adjusting the pH value to 9-11, stirring and reacting under temperature of 45-50? C. for 40-48 hours, then cooling the reaction solution that results to room temperature, slowly pouring the reaction solution into excess absolute ethanol for precipitating the product, filtering and washing the product with absolute ethanol, and drying the product in a drying oven to a constant weight to obtain functionalized modified polyvinyl alcohol; 4) adding 3-5% by volume of a non-ionic surfactant to an oil for preparing an oil phase solution with even stirring; dissolving the functionalized modified polyvinyl alcohol in ionized water to prepare a solution with a concentration of 60-100 g/L, and then pouring it into the oil phase solution slowly for emulsification, adding a cross-linking agent when Tyndall phenomenon is observed, after 4-6 hours, demulsifying the emulsion with ethanol to obtain solid microspheres, filtrating and washing the microspheres with ethanol to obtain modified polyvinyl alcohol embolic microspheres after drying; wherein the organic solvent A in step 1) is one of dimethyl sulfoxide, N, N-dimethylacetamide or formamide; the organic solvent B in step 1) is one of dichloromethane, trichloromethane or dichloroehane.

2. The method of claim 1, wherein in step 1), the polyvinyl alcohol is one of PVA124, PVA1799, PVA1750 or PVA1788.

3. The method of claim 1, wherein in step 1), the concentration of the polyvinyl alcohol solution is 50-120 g/Land the concentration of the acyl chloride solution is 80-150 g/L.

4. The method of claim 1, wherein in step 2), the molar ratio of polyvinyl alcohol to acryloyl chloride or butenoyl chloride is 1:0.2-1.

5. The method of claim 1, wherein in step 2), the acid binding agent is triethylamine or pyridine, and its dosage is 1-1.2 times of the molar number of the acryloyl chloride.

6. The method of claim 1, wherein in step 2) and step 3), a ratio of acryloyl chloride to taurine is 1:1-1.3.

7. The method of claim 1, wherein in step 4), the oil is one of paraffin oil, soybean oil or n-heptane; the volume ratio of the functionalized modified polyvinyl alcohol solution to oil solvent is 1:4-7.

8. (canceled)

9. The method of claim 1, wherein in step 4), the cross-linking agent is 25 wt % glutaraldehyde water solution or epichlorohydrin, and its weight accounts for 3-6% of the weight of functionalized modified polyvinyl alcohol.

10. A method for carrying a drug, comprising loading microspheres prepared by the method claim 1 with doxorubicin.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0022] FIG. 1 Schematic route of the modified polyvinyl alcohol

[0023] FIG. 2 Infrared spectra of the modified polyvinyl alcohol

[0024] FIG. 3 Optical micrograph of the modified polyvinyl alcohol embolic microsphere of sample PVA-S-1

[0025] FIG. 4 X-ray diffraction pattern of PVA and the modified polyvinyl alcohol

[0026] FIG. 5 Swelling performance of the modified polyvinyl alcohol embolic microspheres (in PBS buffer solution with pH=7.4)

[0027] FIG. 6 Drug loading rate of the modified polyvinyl alcohol embolic microspheres at different times

DESCRIPTION OF PREFERRED EMBODIMENTS

Embodiment 1

[0028] The detailed implementation of the invention is further described as follows. The following embodiments are used to illustrate the invention, but not to limit the scope of the invention.

[0029] Step 1): 5 g of polyvinyl alcohol (PVA124) is dissolved in 50 mL dimethyl sulfoxide under stirring to prepare polyvinyl alcohol solution with a concentration of 100 g/L; 10 g of acryloyl chloride is dissolved in 100 mL of dichloromethane to prepare an acryloyl chloride solution with a concentration of 100 g/L;

[0030] Step 2): 50 mL polyvinyl alcohol solution of the step 1 (containing 0.1136 mol PVA) and 2.3 g of triethylamine are added into a 250 mL a three-necked flask; 20.57 mL acryloyl chloride solution of the step 1 (including 0.0227 mol of acryloyl chloride) is dropped into the polyvinyl alcohol solution through a constant pressure drop funnel under stirring at the room temperature for 3 hours, then the temperature is raised to 50? C. for further reaction one hour, then decrease to room temperature. The reaction solution is slowly poured into excess absolute ethanol for precipitating polymer. The polymer is filtered, washed with absolute ethanol, and dried in at 45? C. to constant weight, allyl polyvinyl alcohol is obtained.

[0031] Step 3): The allyl polyvinyl alcohol from the above is putted into 100 mL deionized water under stirring for dissolution; 3.41 g (0.0273 mo) of taurine is dissolved in 100 mL deionized water, and is added to the allyl polyvinyl alcohol solution, adjusting pH 9-11, the reaction is carried out at 4550? C. under stirring for 48 hours; the reaction solution is slowly poured into excess absolute ethanol at the room temperature; the product is precipitated, filtrated, washed with absolute ethanol for three times, and finally dried to constant weight. The modified polyvinyl alcohol is obtained, and the grafting rate (Rg) is calculated according to the following formula:

[00001]$R_g\left(\%\right)=\frac{W_D-W_{\mathrm{PVA}}}{W_{\mathrm{PVA}}}?100$

Where W.sub.D is weight (g) of the dried modified polyvinyl alcohol, and W.sub.PVA is weight (g) of the unmodified polyvinyl alcohol, respectively.

[0032] Step 4): Preparation of embolic microspheres

[0033] 200 mL of paraffin oil is putted into a beaker containing span-80 under stirring evenly; the functionalized modified polyvinyl alcohol is dissolved in 50 mL of deionized water to prepare a PVA solution with a concentration of 100 g/L in advance; then the PVA solution is slowly poured into the paraffin oil under strong mechanical agitation for emulsifying the solution. When Tyndall phenomenon is observed in the emulsion, 1.4 g of glutaraldehyde solution with a concentration of 25 wt % and 1.2 mL of 10 wt % hydrochloric acid are added. The crosslinking reaction is carried out for 4 h at the room temperature, then solid microspheres can be observed after demulsification of the emulsion. The microspheres are filtrated and washed with ethanol for three times. After drying, the modified polyvinyl alcohol eluting microspheres can be obtained. The product symbol is PVA-S-1.

Embodiment 2

[0034] The preparation procedure is similar to Embodiment 1, excepting: [0035] in step 2), changing the addition of triethylamine to 4.6 g; changing the addition of acryloyl chloride solution to 41.14 mL; in step 3), changing the addition of taurine to 6.81 g. The remaining procedures are the same as those in Embodiment 1, to obtain the modified polyvinyl alcohol eluting microspheres with the symbol PVA-S-2.

Embodiment 3

[0036] The preparation procedure is similar to Embodiment 1, excepting: [0037] in step 2), changing the addition of triethylamine to 6.9 g; changing the addition of acryloyl chloride solution to 61.71 mL; in step 3), changing the addition of taurine to 10.21 g. The remaining procedures are the same as those in Embodiment 1, to obtain the modified polyvinyl alcohol eluting microspheres with the symbol PVA-S-3.

Embodiment 4

[0038] The preparation procedure is similar to Embodiment 1, excepting: [0039] in step 2), changing the addition of triethylamine to 9.2 g; changing the addition of acryloyl chloride solution to 82.28 mL; in step 3), changing the addition of taurine to 13.62 g. The remaining procedures are the same as those in Embodiment 1, to obtain the modified polyvinyl alcohol eluting microspheres with the symbol PVA-S-4.

Embodiment 5

[0040] The preparation procedure is similar to Embodiment 1, excepting: [0041] in step 2), changing the addition of triethylamine to 11.5 g; changing the addition of acryloyl chloride solution to 102.85 mL; in step 3), changing the addition of taurine to 17.25 g. The remaining procedures are the same as those in Embodiment 1, to obtain the modified polyvinyl alcohol eluting microspheres with the symbol PVA-S-5.

TABLE-US-00001 TABLE 1 Preparation formula of modified PVA embolic microspheres acryloyl PVA chloride grafting solution.sup.a) solution.sup.b) triethylamine taurine rate Sample (mL) (mL) (g) (g) (%) Embodiment 1 50 20.57 2.3 3.41 12.1 Embodiment 2 50 41.14 4.6 6.81 17.8 Embodiment 3 50 61.71 6.9 10.21 21.5 Embodiment 4 50 82.28 9.2 13.62 24.6 Embodiment 5 50 102.85 11.5 17.25 28.5 .sup.a)Polyvinyl alcohol solution with concentration of 100 g/L; .sup.b): Acryloyl chloride solution with concentration of 100 g/L;

Embodiment 6: Comparative Embodiment

[0042] Preparation of pure polyvinyl alcohol microspheres: adding 200 mL paraffin oil into a 500 mL beaker, dropping 1.9 g of span-80 under mechanical stirring evenly; dissolving 5 g of polyvinyl alcohol (PVA124) in 50 mL of deionized water, then slowly pouring it into the above paraffin oil, emulsifying it with strong mechanical agitation.

[0043] When Tyndall phenomenon is observed in the emulsion, dropping 1.4 g of glutaraldehyde solution with a concentration of 25 wt %, and then dropping 1.2 mL of hydrochloric acid with a concentration of 10 wt %; after reaction for 4 h, demulsifying the emulsion and washing the microspheres with ethanol, to obtain pure polyvinyl alcohol microspheres after drying, with the sample symbol PVA.

Embodiment 7 Characterization of the Modified Polyvinyl Alcohol Eluting Microspheres

[0044] 1. Infrared Spectra

[0045] The prepared modified polyvinyl alcohol embolic microspheres are dried and characterized by total reflection Fourier infrared spectroscopy, with a scanning range of 4000500 cm.sup.?1. It can be seen from FIG. 2 of the drawings that the 33003400 cm.sup.?1 wide peak is ascribed to OH stretching vibration absorption in polyvinyl alcohol; the absorption peak at 2930 cm.sup.?1 is ascribed to methylene CH.sub.2 stretching vibration absorption; the 1710 cm.sup.?1 belongs to C?O absorption peak in ester bond, and the 1185 cm.sup.?1 and 1090 cm.sup.?1 are characteristic absorption peaks of sulfonic acid group; NH bending vibration peak appears at 1570 cm.sup.?1, CN stretching vibration absorption peak appears at 1267 cm.sup.?1, and CO stretching vibration absorption peak appears at 1033 cm.sup.?1, respectively.

[0046] 2. Optical Micrograph

[0047] The modified PVA eluting microspheres PVA-S-1 in the swelling state are placed on the glass slide, adjusting the magnification of the optical microscope for observation of the morphology of the microspheres. The results in FIG. 3 show that the appearance of the microspheres is regular spherical and the color is bright white. There is no adhesion among the microspheres with diameter of 220?350 ?m.

[0048] 3. X-Ray Diffraction Pattern

[0049] The X-ray diffraction (XRD) results of PVA and modified polyvinyl alcohol are shown in FIG. 4. It can be seen that the crystal face (101) sharp diffraction peak of PVA appears at 19.7? (20). When the PVA is modified, the position of its characteristic diffraction peak is basically unchanged, but the strength is weakened and the peak shape is widened, which indicates that the crystal structure of PVA is consistent before and after modification, but the crystallinity is greatly reduced after modification. At the same time, it is found that with the increase of the modification degree, the intensity of the crystallization peak decreased significantly. This is because the introduction of taurine molecules into the side chain of PVA destroys the regularity of the PVA chain segment, so that the hydrogen bond association is weakened, and its crystallization capacity is reduced. Therefore, the crystal characteristics are weakened, indicating that the intensity of the diffraction peak decreased.

[0050] 4. Swelling Property

[0051] The dried modified polyvinyl alcohol eluting microspheres are added to PBS buffer solution with pH=7.4 for swelling at a constant temperature of 37?0.5? C. The swelled microspheres are taken out at different time points, and are weighed. The swelling ratio SR (%) is calculated according to the following formula.

[00002]$S_R\left(\%\right)=\frac{W_1-W_0}{W_0}?100$

Where W.sub.0 and W.sub.1 are the weights of the microspheres before and after swelling, respectively

[0052] It can be seen from FIG. 5 that the swelling ratio of microspheres increases rapidly in the first one hour, then increases slowly, and reaches the equilibrium swelling within 2 h. With the increase of grafting degree of taurine in the microspheres, the swelling ratio of the microspheres increased from PVA-S-1 to PVA-S-5, because taurine molecules contain hydrophilic group of SO.sub.3H, which leads to the increase of the swelling ratio of the microspheres in the swelling process. As a comparison, the swelling ratios of all modified samples are higher than that of the unmodified PVA microspheres. As described above, the hydrophilic groups of SO.sub.3H are introduced into the side chains of the modified PVA, which increases the water absorption performance.

Embodiment 8

[0053] Preparation of drug loaded modified PVA embolic microspheres: adding 30 mg of the modified PVA embolic microsphere to 6 mL of doxorubicin hydrochloride deionized water solution with a concentration of 4 mg/mL, filtering the microspheres after 5 hours reaction, washing the surface of the microspheres with deionized water, merging the washing solution into doxorubicin hydrochloride solution, measuring the absorbance of doxorubicin hydrochloride solution at 483 nm on an ultraviolet spectrophotometer, and calculating the drug loading rate of the microspheres. The microspheres are dried at 55? C. for 24 hours to obtain drug loaded embolic microspheres.

[0054] The drug loading rate (L.sub.R) of microspheres is calculated according to the following formula:

[00003]$L_R\left(\%\right)=\frac{W_D}{W_S}?100$

Where W.sub.D is the mass of the drug adsorbed by the microspheres (mg); W.sub.S is the mass of the microspheres (mg).

[0055] FIG. 6 shows the drug loading kinetics curves of several modified PVA embolic microspheres in doxorubicin hydrochloride solution. It is observed that the drug loading rate and drug loading speed of the microspheres increased from PVA-S-1 to PVA-S-5. The high drug loading rate and loading speed are due to two reasons: first, sulfonic acid groups have been introduced into the modified PVA microspheres, the sulfonic acid groups and doxorubicin hydrochloride undergo an ion exchange drug loading mode, which directly improves the drug loading rate. Second, the introduction of taurine molecules into the side chain of PVA destroys the regular arrangement and partial crystallinity of PVA chain segments, increases the internal micropores and channels of the microspheres, and is also conducive to the diffusion of drug molecules. At the same time, the improvement of the internal structure of the microspheres also improves the efficiency of drug loading in physical ways. The combined effect of these factors leads to the improvement of drug loading rate and drug loading speed.