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离子交联作为一种调节基于多糖共混物的口腔粘膜粘附性微粒性质的策略。

Ionic Cross-Linking as a Strategy to Modulate the Properties of Oral Mucoadhesive Microparticles Based on Polysaccharide Blends.

作者信息

Boni Fernanda Isadora, Cury Beatriz S F, Ferreira Natália Noronha, Gremião Maria Palmira Daflon

机构信息

School of Pharmaceutical Science, São Paulo State University (UNESP), Araraquara, Road Araraquara-Jaú, Km 01, Araraquara, São Paulo 14801-902, Brazil.

出版信息

Pharmaceutics. 2021 Mar 19;13(3):407. doi: 10.3390/pharmaceutics13030407.

Abstract

Polymer blends of gellan gum (GG)/retrograded starch(RS) and GG/pectin (P) were cross-linked with calcium, aluminum, or both to prepare mucoadhesive microparticles as oral carriers of drugs or nano systems. Cross-linking with different cations promoted different effects on each blend, which can potentially be explored as novel strategies for modulating physical-chemical and mucoadhesive properties of microparticles. Particles exhibited spherical shapes, diameters from 888 to 1764 µm, and span index values lower than 0.5. Blends of GG:P cross-linked with aluminum resulted in smaller particles than those obtained by calcium cross-linking. GG:RS particles exhibited larger sizes, but cross-linking this blend with calcium promoted diameter reduction. The uptake rates of acid medium were lower than phosphate buffer (pH 6.8), especially GG:RS based particles cross-linked with calcium. On the other hand, particles based on GG:P cross-linked with calcium absorbed the highest volume of acid medium. The percentage of systems erosion was higher in acid medium, but apparently occurred in the outermost layer of the particle. In pH 6.8, erosion was lower, but caused expressive swelling of the matrixes. Calcium cross-linking of GG:RS promoted a significantly reduction on enzymatic degradation at both pH 1.2 and 6.8, which is a promising feature that can provide drug protection against premature degradation in the stomach. In contrast, GG:P microparticles cross-linked with calcium suffered high degradation at both pH values, an advantageous feature for quickly releasing drugs at different sites of the gastrointestinal tract. The high mucoadhesive ability of the microparticles was evidenced at both pH values, and the Freundlich parameters indicated stronger particle-mucin interactions at pH 6.8.

摘要

结冷胶(GG)/回生淀粉(RS)和GG/果胶(P)的聚合物共混物与钙、铝或两者交联,以制备作为药物口服载体或纳米系统的粘膜粘附微粒。与不同阳离子交联对每种共混物产生不同影响,这有可能被探索为调节微粒物理化学和粘膜粘附特性的新策略。微粒呈球形,直径为888至1764 µm,跨度指数值低于0.5。与铝交联的GG:P共混物产生的颗粒比钙交联得到的颗粒更小。GG:RS颗粒尺寸更大,但将该共混物与钙交联可促进直径减小。酸性介质的摄取率低于磷酸盐缓冲液(pH 6.8),尤其是与钙交联的基于GG:RS的颗粒。另一方面,与钙交联的基于GG:P的颗粒吸收酸性介质的量最高。在酸性介质中系统侵蚀的百分比更高,但显然发生在颗粒的最外层。在pH 6.8时,侵蚀较低,但导致基质明显肿胀。GG:RS的钙交联在pH 1.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1621/8035971/cb8624ddaaa2/pharmaceutics-13-00407-g001.jpg

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