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[利用逐层沉积技术制备功能性聚合物薄膜]

[Development of Functional Thin Polymer Films Using a Layer-by-Layer Deposition Technique].

作者信息

Yoshida Kentaro

机构信息

School of Pharmaceutical Sciences, Ohu University.

出版信息

Yakugaku Zasshi. 2017;137(10):1215-1221. doi: 10.1248/yakushi.17-00128.

DOI:10.1248/yakushi.17-00128
PMID:28966262
Abstract

Functional thin films containing insulin were prepared using layer-by-layer (LbL) deposition of insulin and negatively- or positively-charged polymers on the surface of solid substrates. LbL films composed of insulin and negatively-charged polymers such as poly(acrylic acid) (PAA), poly(vinylsulfate) (PVS), and dextran sulfate (DS) were prepared through electrostatic affinity between the materials. The insulin/PAA, insulin/PVS, and insulin/DS films were stable in acidic solutions, whereas they decomposed under physiological conditions as a result of a change in the net electric charge of insulin from positive to negative. Interestingly, the insulin-containing LbL films were stable even in the presence of a digestive-enzyme (pepcin) at pH 1.4 (stomach pH). In contrast, LbL films consisting of insulin and positively-charged polymers such as poly(allylamine hydrochloride) (PAH) decomposed in acidic solutions due to the positive charges of insulin generated in acidic media. The insulin-containing LbL films can be prepared not only on the surface of flat substrates, such as quartz slides, but also on the surface of microparticles, such as poly(lactic acid) (PLA) microbeads. Thus, insulin-containing LbL film-coated PLA microbeads can be handled as a powder. In addition, insulin-containing microcapsules were prepared by coating LbL films on the surface of insulin-doped calcium carbonate (CaCO) microparticles, followed by dissolution of the CaCO core. The release of insulin from the microcapsules was accelerated at pH 7.4, whereas it was suppressed in acidic solutions. These results suggest the potential use of insulin-containing microcapsules in the development of oral formulations of insulin.

摘要

通过在固体基质表面逐层(LbL)沉积胰岛素与带负电荷或正电荷的聚合物,制备了含胰岛素的功能薄膜。由胰岛素与带负电荷的聚合物(如聚丙烯酸(PAA)、聚乙烯硫酸盐(PVS)和硫酸葡聚糖(DS))组成的LbL薄膜是通过材料间的静电亲和力制备的。胰岛素/PAA、胰岛素/PVS和胰岛素/DS薄膜在酸性溶液中稳定,而在生理条件下会分解,这是由于胰岛素净电荷从正变为负所致。有趣的是,含胰岛素的LbL薄膜即使在pH 1.4(胃pH值)的消化酶(胃蛋白酶)存在下也很稳定。相比之下,由胰岛素与带正电荷的聚合物(如聚烯丙胺盐酸盐(PAH))组成的LbL薄膜在酸性溶液中会分解,因为在酸性介质中胰岛素会产生正电荷。含胰岛素的LbL薄膜不仅可以在平面基质(如石英载玻片)表面制备,还可以在微粒(如聚乳酸(PLA)微珠)表面制备。因此,含胰岛素的LbL薄膜包覆的PLA微珠可以作为粉末处理。此外,通过在掺杂胰岛素的碳酸钙(CaCO₃)微粒表面包覆LbL薄膜,然后溶解CaCO₃核,制备了含胰岛素的微胶囊。胰岛素从微胶囊中的释放在pH 7.4时加速,而在酸性溶液中受到抑制。这些结果表明含胰岛素微胶囊在胰岛素口服制剂开发中的潜在用途。

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