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MICROENCAPSULATION OF PROTEINS WITHIN CACO_3 MICROSPHERES USING SUPERCRITICAL CO_2 MEDIA

机译:使用超临界CO_2培养基中Caco_3微球内蛋白质的微胶囊

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This study is a preliminary work of a global project aiming at conceiving and characterizing implantable synthetic extracellular matrices seeded with calcium carbonate multifunctional particles and releasing therapeutic biomolecules, for bone and cartilage tissue engineering. The formulation method of CaCO_3 microparticles is based on the formation of an emulsion of water in SC-CO_2 (W/C). Hollow and spherical microparticles with a 5 urn diameter were successfully obtained and fully characterized. Encapsulation experiments were carried out using lysozyme as model protein. Encapsulation yield and lysozyme loading can reach respectively up to 60 % and 7 %. Moreover, protein release kinetics have been determined during 24 hours. Results were compared and discussed with the literature ones related to microencapsulation of lysozyme and other biomolecules within CaCO_3 particles. Hence, it permitted to bring out a proof of the concept of this emulsification process [1] for the encapsulation of model and therapeutic biomolecules.
机译:本研究是一个全球项目的初步工作,旨在构思和表征含有碳酸钙多功能颗粒和释放治疗生物分子的植入合成细胞外基质,用于骨和软骨组织工程。 CaCO_3微粒的配方方法基于SC-CO_2(W / C)中的水乳液的形成。成功地获得了具有5瓮直径的空心和球形微粒并完全表征。使用溶菌酶作为模型蛋白进行封装实验。封装产量和溶菌酶负荷可分别达到60%和7%。此外,在24小时内已经确定了蛋白质释放动力学。比较结果和讨论与CaCOzyme和CaCO_3颗粒内的其他生物分子相关的文献中的文献。因此,它允许发出该乳化过程的概念证明[1]用于封装模型和治疗生物分子。

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