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Development of an injectable PHBV microparticles-GG hydrogel hybrid system for regenerative medicine

机译:再生医学用注射用PHBV微粒-GG水凝胶混合体系的开发

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摘要

Uncontrollable displacements that greatly affect the concentration of active agents at the target tissues are among a major limitation of the use of microparticulate drug delivery systems (DDS). Under this context a biphasic injectable DDS combining poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV) microparticles (MPs) and a gellan gum (GG) injectable hydrogel is herein proposed for the localized delivery and long-term retention of MPs carrying hydrophilic and hydrophobic model active agents. A double emulsion-solvent evaporation method was adopted to develop the PHBV MPs, carrying bovine serum albumin (BSA) or dexamethasone (Dex) as hydrophilic and hydrophobic active agents’ models, respectively. Moreover, this method was modified, together with the properties of the hydrogel to tailor the delivery profile of the active agents. Variations of the composition of the organic phase during the process allowed tuning surface topography, particle size distribution and core porosity of the PHBV MPs and, thus, the in vitro release profile of Dex but not of BSA. Besides, after embedding hydrogels of higher GG concentration led to a slower and more sustained release of both active agents, independently of the processing conditions of the microparticulate system.
机译:极大地影响靶组织中活性剂浓度的失控置换是使用微粒药物递送系统(DDS)的主要限制之一。在这种情况下,本文提出了结合聚(羟基丁酸酯-共-羟基戊酸酯)(PHBV)微粒(MP)和结冷胶(GG)可注射水凝胶的双相可注射DDS,用于局部递送和长期保留携带亲水性和疏水性的MP模拟活动代理。 PHBV MPs采用双乳剂-溶剂蒸发法开发,分别以牛血清白蛋白(BSA)或地塞米松(Dex)为亲水和疏水活性剂模型。此外,对该方法以及水凝胶的性质进行了修改,以调整活性剂的递送特性。在此过程中有机相组成的变化允许调整PHBV MP的表面形貌,粒径分布和核心孔隙率,因此可以调整Dex而不是BSA的体外释放曲线。此外,在包埋较高GG浓度的水凝胶后,与两种微粒的加工条件无关,导致两种活性剂的释放更缓慢,更持续。

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