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A Novel Preparation Method For PLGA Microspheres Using Non Toxic Solvent Emulsified In Supercritical CO_2

机译:使用超临界CO_2中乳化的非毒性溶剂的PLGA微球的新制备方法

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Purpose. To generate biodegradable poly(lactic-co-glycolic acid) (PLGA) microparticles without using volatile organic solvent for a sustained protein release. Methods. The formulation of microparticles is based on the formation of an emulsion of polymer solution in CO_2 medium. Polymer solution was prepared in injectable non-volatile solvent such as glycofurol or isosorbide dimethyl ether. Moreover, encapsulation experiments were carried out using lysozyme as model protein. An experimental design was built-up to go further in the understanding of the system and to better predict the encapsulation yield. Results. Spherical microparticles were successfully generated. Encapsulation yield of lysozyme can reach up to about 85% within our chosen ranges of parameters. Conclusion. This method with the use of non-toxic solvents is suitable for the preparation of PLGA microspheres. Further characterization step will be performed to confirm its utility in controlled release of therapeutic protein.
机译:目的。在不使用挥发性有机溶剂的情况下产生可生物降解的聚(乳酸二乙醇酸)(PLGA)微粒以进行持续的蛋白质释放。方法。微粒的制剂基于在CO_2培养基中形成聚合物溶液的乳液。将聚合物溶液在注射的非挥发性溶剂如糖醛罗酚或异山梨醇二甲醚中制备。此外,使用溶菌酶作为模型蛋白进行封装实验。建立实验设计,以进一步了解系统,并更好地预测封装产量。结果。成功产生球形微粒。在我们所选择的参数范围内,溶菌酶的包封产率可达约85%。结论。使用无毒溶剂的这种方法适用于制备PLGA微球。将进行进一步表征步骤以确认其在治疗蛋白的受控释放中的效用。

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