Study of Pneumococcal Surface Protein, PspA, Incorporated in Poly(Vinyl Alcohol) Hydrogel Membranes

Hazim S. Aljewari, MT Romo Castro, Olivia Solomon, Quincy C. Moore, F. Nave, A. Thompson
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引用次数: 2

Abstract

This study investigates poly(vinyl alcohol) (PVA) membranes as controlled release micro-matrices, which can be useful in therapeutic applications for optimizing the administration of drugs. Currently, the use of hydrogels is limited by protein size. This study investigates the delivery of PspA, a large protein of approximately 38 kD. Pneumococcal surface protein A (PspA) has been shown to provide protective immunity against pneumococcal infection and is considered as a pneumococcal vaccine. The protein release experiments demonstrated that from an initial pH 7.4, approximately 60% of PspA diffuse into a neutral environment with an initial burst and a declining rate reaching equilibrium. The results indicate that the protein was successfully incorporated and released from the membrane over time. The hydrogel and protein interaction is temporary, and the membrane system is ideal for protein drug delivery. The data confirm that the protein did not aggregate and was active after release. The protein release is promising and a step forward to develop microneedles to facilitate high molecular weight protein delivery as well as vaccine delivery.
聚乙烯醇水凝胶膜中肺炎球菌表面蛋白(PspA)的研究
本研究探讨聚乙烯醇(PVA)膜作为控释微基质,可用于优化药物给药的治疗应用。目前,水凝胶的使用受到蛋白质大小的限制。本研究研究了PspA的传递,PspA是一种约38 kD的大蛋白。肺炎球菌表面蛋白A (PspA)已被证明对肺炎球菌感染提供保护性免疫,被认为是一种肺炎球菌疫苗。蛋白质释放实验表明,从初始pH 7.4开始,大约60%的PspA扩散到中性环境中,初始爆发并以下降的速率达到平衡。结果表明,随着时间的推移,蛋白质被成功地结合并从膜中释放出来。水凝胶和蛋白质的相互作用是暂时的,膜系统是理想的蛋白质药物输送。数据证实,该蛋白在释放后没有聚集并具有活性。蛋白质释放是有希望的,并且是开发微针以促进高分子量蛋白质递送和疫苗递送的一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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