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盐酸苯海拉明负载的中性微粒用乙基纤维素水分散体包衣后的控释行为。

Controlled-release behavior of diphenhydramine hydrochloride loaded neutral microgranules and coated using ethylcellulose water dispersion.

作者信息

Opota D O, Joachim G, Kalantzis G, Piccerelle P, Reynier J P, Joachim J

机构信息

Laboratoire de Pharmacie Galénique et Cosmétologie, Faculté de Pharmacie, Marseille, France.

出版信息

Drug Dev Ind Pharm. 1999 Jan;25(1):81-7. doi: 10.1081/ddc-100102145.

Abstract

The development of a loading method of a water-soluble drug using aqueous binding solution to produce microgranules that were then coated with an aqueous ethylcellulose dispersion to sustain drug release is described. The results, in terms of drug used, showed that besides the fluidized bed parameters, the amount of drug dissolved in the binder solution plays an important role in obtaining a satisfying result during the spraying process. Thus, it seems necessary to determine the critical concentration above which the material started to adhere to the interior of the fluidization column, and the possibility of drug layering onto carrier material is aggravated. ANOVA of the time parameter for release of 63.2% of total drug (td) value showed significant influence of ethylcellulose (Aquacoat ECD-30) and dibutyl sebacate concentration on diphenhydramine hydrochloride (DPH) release. The dissolution rate decreased with an increase in polymer concentration. The diffusional exponent n of the Peppas equation indicated that the DPH release kinetic was non-Fickian but approached Fickian diffusion, particularly at higher coating levels.

摘要

描述了一种使用水性粘合剂溶液制备水溶性药物微颗粒的负载方法,该微颗粒随后用水性乙基纤维素分散体包衣以实现药物缓释。就所用药物而言,结果表明,除了流化床参数外,溶解在粘合剂溶液中的药物量在喷雾过程中获得满意结果方面起着重要作用。因此,似乎有必要确定临界浓度,超过该浓度材料开始粘附在流化柱内部,并且药物分层到载体材料上的可能性会增加。对总药物释放63.2%的时间参数(td值)进行方差分析表明,乙基纤维素(Aquacoat ECD - 30)和癸二酸二丁酯浓度对盐酸苯海拉明(DPH)释放有显著影响。溶解速率随聚合物浓度的增加而降低。Peppas方程的扩散指数n表明,DPH释放动力学是非菲克ian的,但接近菲克扩散,特别是在较高包衣水平时。

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