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聚(丙交酯-乙交酯)植入物热熔挤出法制备过程中蛋白质的释放:硫酯形成是不完全释放的原因。

Protein release from poly(lactide-co-glycolide) implants prepared by hot-melt extrusion: thioester formation as a reason for incomplete release.

机构信息

College of Pharmacy, Freie Universität Berlin, Kelchstrasse 31, 12169 Berlin, Germany.

出版信息

Int J Pharm. 2012 Nov 15;438(1-2):302-6. doi: 10.1016/j.ijpharm.2012.09.015. Epub 2012 Sep 16.

Abstract

The aim of this study was to characterize the protein release from PLGA-based implants prepared by hot-melt extrusion with special emphasis on identifying reasons for incomplete release. Biodegradable PLGA-implants loaded with BSA were prepared with a syringe-die extrusion device. A burst-free release was achieved up to 25% BSA loading by milling the protein prior to extrusion. The release was incomplete at 70% at loadings below the percolation threshold of the protein; higher protein loadings increased the release to 97%. However, an insoluble implant mass remained for over 180 days, which was attributed to the acylation of BSA by PLGA oligomers via a thioester bond. The incomplete protein release due to the formation of this covalent bond was overcome when increasing the porosity of the implant, which effectively reduced the contact between BSA and PLGA oligomers. Accordingly, melt-extrusion facilitated incorporating high loadings of BSA into burst-free biodegradable implants. Additionally, it enhanced complete protein release by a process- or formulation controlled increase of the implant porosity.

摘要

本研究旨在描述通过热熔挤出法制备的基于 PLGA 的植入物中的蛋白质释放特性,特别强调确定不完全释放的原因。采用注射器挤出装置制备载有 BSA 的可生物降解 PLGA 植入物。通过在挤出前对蛋白质进行研磨,实现了高达 25% BSA 载量的无突释释放。在低于蛋白质渗透阈值的载量下,释放不完全,达到 70%;较高的蛋白质载量可将释放提高到 97%。然而,超过 180 天仍有不可溶的植入物质量残留,这归因于 BSA 通过 PLGA 低聚物的硫酯键发生酰化。通过增加植入物的孔隙率来克服由于形成这种共价键导致的不完全蛋白质释放,这有效地减少了 BSA 和 PLGA 低聚物之间的接触。因此,熔融挤出法有助于将高载量的 BSA 纳入无突释的可生物降解植入物中。此外,通过增加植入物孔隙率的过程或配方控制来增强完全的蛋白质释放。

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