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作为一种粘膜粘附聚合物的亚麻籽粘液的提取、表征及评价。 (注:Linn. 一般指亚麻籽,这里按照常见情况进行了补充翻译,仅为符合完整语义的推测性补充,具体含义需结合原文更多背景信息确定)

Extraction, Characterization, and Evaluation of Linn. Mucilage as a Mucoadhesive Polymer.

作者信息

Embafrash Berhe Hailemichael, Tesfay Mezgebo Desta, Abrha Solomon, Gebremeskel Haile Tsadkan, Molla Fantahun

机构信息

Department of Pharmacy, Ayder Comprehensive and Specialized Hospital, College of Health Sciences, Mekelle University, P.O. Box 1871, Mekelle, Ethiopia.

Department of Pharmaceutics, School of Pharmacy, College of Health Sciences, Mekelle University, P.O. Box 1871, Mekelle, Ethiopia.

出版信息

Adv Pharmacol Pharm Sci. 2023 Aug 14;2023:5535344. doi: 10.1155/2023/5535344. eCollection 2023.

Abstract

Being biocompatible, less toxic, cheap, easily available, and environmentally friendly, there is an increased trust in natural polymers in the drug delivery system. Mucilages, among the natural polymers, are the primary metabolites of plants that have been widely utilized in pharmaceutical manufacturing for different purposes, and mucoadhesive is one among them. The present study was designed to investigate the use of LSM as a mucoadhesive polymer using ibuprofen as a model drug. The mucilage was extracted following an aqueous extraction method and its percentage yield was found to be 13.2% w/w. Besides, three microsphere formulations of ibuprofen were prepared using synthetic polymer hydroxyl propyl methyl cellulose (HPMC) K100M and the LSM in polymer to drug ratios of 1 : 1, 1 : 5, and 3 : 5 by applying ionotropic gelation followed by solvent evaporation methods. The microspheres were evaluated for various micromeritic properties and all the formulations exhibited free-flowing properties. Optical microscopic pictures of almost all the microspheres except F3 and F6 (which had more or less spherical shapes) were found to have irregular and discrete shapes. Besides, the surfaces of all the formulations were rough in texture. The drug entrapment efficiency of the microspheres was found to be between 52.08% ± 0.80 and 87.97% ± 0.72. The wash-off test evidenced that almost 50 percent (especially F3) of the microspheres were able to adhere up to 18 h and showed remarkable bioadhesion properties. The drug release profile indicated that all the formulations were able to prolong their drug release up to 12 h with a non-fickian release mechanism, except for F4, which followed a fickian release. Therefore, based on the findings of this study, LSM can be used as a potential alternative mucoadhesive excipient for sustained release formulations.

摘要

由于具有生物相容性、低毒性、价格低廉、易于获取且环境友好等特点,药物递送系统中对天然聚合物的信任度日益增加。在天然聚合物中,黏液质是植物的主要代谢产物,已被广泛用于不同目的的药物制造,黏膜黏附剂就是其中之一。本研究旨在以布洛芬为模型药物,研究刺云实胶作为黏膜黏附聚合物的用途。采用水提法提取黏液质,其得率为13.2%(w/w)。此外,通过离子凝胶法继以溶剂蒸发法,使用合成聚合物羟丙基甲基纤维素(HPMC)K100M和刺云实胶,以聚合物与药物比例为1∶1、1∶5和3∶5制备了三种布洛芬微球制剂。对微球的各种粉体学性质进行了评估,所有制剂均表现出自由流动性质。除F3和F6(形状或多或少为球形)外,几乎所有微球的光学显微镜照片显示其形状不规则且离散。此外,所有制剂的表面质地粗糙。微球的药物包封率在52.08%±0.80至87.97%±0.72之间。洗脱试验证明,近50%(尤其是F3)的微球能够黏附长达18小时,并表现出显著的生物黏附特性。药物释放曲线表明,除F4呈现菲克扩散释放外,所有制剂均能够通过非菲克扩散释放机制将药物释放延长至12小时。因此,基于本研究结果,刺云实胶可作为一种潜在的替代黏膜黏附辅料用于缓释制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06e/10442183/5eb893af1f44/APS2023-5535344.001.jpg

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