壳聚糖-微晶纤维素共混物作为直接压缩赋形剂的评价。

Journal of drug delivery Pub Date : 2017-01-01 Epub Date: 2017-12-19 DOI:10.1155/2017/8563858
Emmanuel O Olorunsola, Grace A Akpan, Michael U Adikwu
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引用次数: 17

摘要

本研究旨在评价壳聚糖-微晶纤维素共混物作为直接压缩赋形剂的性能。对蟹壳壳聚糖、α-乳糖一水和微晶纤维素粉末进行了表征。将微晶纤维素和壳聚糖按9:1、4:1、2:1和1:1的比例共混制成直接压缩赋形剂,占甲硝唑片的60%。还生产了含有微晶纤维素和α-乳糖一水合物混合物的类似片剂以及含有纯微晶纤维素的片剂。测定了片剂的致密度、抗拉强度、孔隙率、崩解时间和溶出度。与微晶纤维素和乳糖相比,壳聚糖具有较高的含水率(7.66%)和较高的吸湿能力(1.33%)。其流动性能也较好(Carr’s index为18.9%,Hausner’s ratio为1.23)。随着壳聚糖含量的增加,片剂的压实密度增加,抗拉强度降低。与乳糖相比,随着壳聚糖比例的增加,崩解时间延长,溶出速率降低。研究表明,壳聚糖能促进粉剂的流动性和片剂的快速崩解。然而,加入等比例的微晶纤维素和壳聚糖可以生产缓释片。因此,壳聚糖在低浓度时促进片剂的崩解,在高浓度时促进片剂的缓释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of Chitosan-Microcrystalline Cellulose Blends as Direct Compression Excipients.

Evaluation of Chitosan-Microcrystalline Cellulose Blends as Direct Compression Excipients.

Evaluation of Chitosan-Microcrystalline Cellulose Blends as Direct Compression Excipients.

This study was aimed at evaluating chitosan-microcrystalline cellulose blends as direct compression excipients. Crab shell chitosan, α-lactose monohydrate, and microcrystalline cellulose powders were characterized. Blends of the microcrystalline cellulose and chitosan in ratios 9 : 1, 4 : 1, 2 : 1, and 1 : 1 as direct compression excipients were made to constitute 60% of metronidazole tablets. Similar tablets containing blends of the microcrystalline cellulose and α-lactose monohydrate as well as those containing pure microcrystalline cellulose were also produced. The compact density, tensile strength, porosity, disintegration time, and dissolution rate of tablets were determined. Chitosan had higher moisture content (7.66%) and higher moisture sorption capacity (1.33%) compared to microcrystalline cellulose and lactose. It also showed better flow properties (Carr's index of 18.9% and Hausner's ratio of 1.23). Compact density of tablets increased but tensile strength decreased with increase in the proportion of chitosan in the binary mixtures. In contrast to lactose, the disintegration time increased and the dissolution rate decreased with increase in the proportion of chitosan. This study has shown that chitosan promotes flowability of powder mix and rapid disintegration of tablet. However, incorporation of equal proportions of microcrystalline cellulose and chitosan leads to production of extended-release tablet. Therefore, chitosan promotes tablet disintegration at low concentration and enables extended-release at higher concentration.

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来源期刊
Journal of drug delivery
Journal of drug delivery PHARMACOLOGY & PHARMACY-
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