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用邻苯二甲酸纤维素制备的喷雾干燥产品中盐酸罂粟碱的药物可利用度。

Pharmaceutical availability of papaverine hydrochloride from spray-dried products prepared with cellulose phthalates.

作者信息

Senjković R, Bećirević M, Rudić J

机构信息

Faculty of Pharmacy and Biochemistry, University of Zagreb, Yugoslavia.

出版信息

Pharmazie. 1990 Oct;45(10):749-51.

PMID:2089385
Abstract

Papaverine hydrochloride suspensions in acetone/methanol (1:1) solutions of cellulose acetate phthalate, hydroxypropylmethyl cellulose phthalate HP 50 and HP 55 were spray-dried by means of Aeromatic, type Strea-1 device. Encapsulated particles were characterized by drug content, average volume-surface, flow rates, and porosities. Encapsulated products were compressed with and without additives (10% corn starch, 3% talc and 1.5% magnesium stearate). Dissolution tests of the compressed tablets in water were evaluated. The results of the dissolution of papaverine hydrochloride from directly compressed encapsulated particles were linearized by the Higuchi model, while for compressed tablets containing adjuvants a third root of undissolved drug vs. time model was used. The kind, quantity and technology of compressed tablets production influenced the drug release.

摘要

采用Aeromatic公司的Strea-1型设备对盐酸罂粟碱悬浮液在醋酸邻苯二甲酸纤维素、羟丙基甲基纤维素邻苯二甲酸酯HP 50和HP 55的丙酮/甲醇(1:1)溶液中进行喷雾干燥。通过药物含量、平均体积-表面积、流速和孔隙率对包封颗粒进行表征。对包封产品在有无添加剂(10%玉米淀粉、3%滑石粉和1.5%硬脂酸镁)的情况下进行压片。评估压片在水中的溶出度测试。直接压片的包封颗粒中盐酸罂粟碱的溶出结果通过Higuchi模型进行线性化处理,而对于含有辅料的压片,则使用未溶解药物的立方根与时间模型。压片生产的种类、数量和工艺会影响药物释放。

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