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用于鼻内给药的载5-氟尿嘧啶壳聚糖微球的制备及性质

Preparation and Properties of 5-Fluorouracil-Loaded Chitosan Microspheres for the Intranasal Administration.

作者信息

Li Wanqing, Ba Hongyuan, Huang Peng, Zheng Aiping, Yang Xi

机构信息

School of Preclinical Medicine, Beijing University of Chinese Medicine Beijing, China.

Academy of Sports Medicine and Physiotherapy, Beijing Sport University Beijing, China.

出版信息

Drug Res (Stuttg). 2018 Dec;68(12):673-679. doi: 10.1055/a-0586-8406. Epub 2018 Jul 2.

Abstract

OBJECTIVE

To study the preparation technique of 5-fluorouracil and the release characteristic of 5-fluorouracil-loaded chitosan microspheres for the intranasal administration.

METHODS

5-fluorouracil-loaded chitosan microspheres were prepared by emulsion chemical cross-link technique. The orthogonal experimental design was used to optimize the preparation procedure. Dynamic dialysis method was applied to determine the release characteristic of microspheres in vitro and its influencing factors. Swelling behavior was expressed by swelling ratio. The degree of mucoadhesion was investigated by determining the mucociliary transport rate(MTR) of the microparticle across a frog palate.

RESULTS

Microspheres with a good shape and narrow size distribution were prepared. The average diameter was 43±4 μm. The drug loading was (38.5±1.0) %. The entrapment efficiency was (79.0±1.8) %. The drug release profile in vitro could be described by Higuichi eqution as Q=0.1035t+0.0284 (r=0.9965). Chitosan had good mucoadhesive property and caused a significant reduction in MTR(P<0.01).

CONCLUSION

The optimized technique has a good reproducibility and a high entrapment efficiency, so it could be used to prepare 5-fluorouracil-loaded chitosan microspheres for the intranasal administration.Chitosan is a good material for nasal preparation and has prospective development in the pharmaceutical field.

摘要

目的

研究5-氟尿嘧啶的制备工艺及5-氟尿嘧啶壳聚糖微球的鼻腔给药释放特性。

方法

采用乳化化学交联技术制备5-氟尿嘧啶壳聚糖微球。运用正交试验设计优化制备工艺。采用动态透析法测定微球的体外释放特性及其影响因素。用溶胀率表示溶胀行为。通过测定微球在蛙腭上的黏液纤毛转运速率(MTR)来研究黏附程度。

结果

制备出形状良好、粒径分布窄的微球。平均粒径为43±4μm。载药量为(38.5±1.0)%。包封率为(79.0±1.8)%。体外药物释放曲线可用Higuichi方程描述为Q = 0.1035t + 0.0284(r = 0.9965)。壳聚糖具有良好的黏附性,可使MTR显著降低(P < 0.01)。

结论

优化后的工艺具有良好的重现性和较高的包封率,可用于制备鼻腔给药的5-氟尿嘧啶壳聚糖微球。壳聚糖是一种良好的鼻腔制剂材料,在药学领域具有广阔的发展前景。

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