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含微溶性药物的双相释放片的制剂

Formulation of biphasic release tablets containing slightly soluble drugs.

作者信息

Maggi L, Machiste E O, Torre M L, Conte U

机构信息

Dipartimento di Chimica Farmaceutica, University of Pavia, Pavia, Italy.

出版信息

Eur J Pharm Biopharm. 1999 Jul;48(1):37-42. doi: 10.1016/s0939-6411(99)00019-3.

Abstract

A new biphasic release system for slightly soluble drugs has been proposed. To enhance the dissolution rate, the drug was milled with a superdisintegrant. Then, double-layer tablets were prepared. One layer was formulated to release the drug in a very short time (fast-release). The other consisted of an extended-release hydroxypropylmethylcellulose (HPMC) matrix. Different HPMC concentrations (10, 16 and 22%) and viscosity grades (Methocel K4, K15 and K100M) were used to obtain different release rates of the drug from the extended-release layer, ketoprofen and praziquantel were used as slightly soluble model drugs. The in vitro dissolution tests of the prepared double-layer systems, showed the desired biphasic behaviour: the drug contained in the fast releasing layer dissolved within the first 15 min, while the drug contained in the prolonged-release layer was released at different times, depending on the formulation of the hydrophilic matrix. In particular, an increase in the percentage and viscosity grade of HPMC, in the extended release layer, leads to a decrease in the drug delivery rate and produces a wide range of different release rates from only a few hours up to 24 h.

摘要

已提出一种用于微溶性药物的新型双相释放系统。为提高溶出速率,将药物与超级崩解剂一起研磨。然后,制备双层片剂。一层被设计为在极短时间内释放药物(速释)。另一层由缓释羟丙基甲基纤维素(HPMC)基质组成。使用不同的HPMC浓度(10%、16%和22%)和粘度等级(Methocel K4、K15和K100M)来获得药物从缓释层的不同释放速率,酮洛芬和吡喹酮用作微溶性模型药物。所制备的双层系统的体外溶出试验显示出所需的双相行为:速释层中的药物在最初15分钟内溶解,而缓释层中的药物在不同时间释放,这取决于亲水性基质的配方。特别是,缓释层中HPMC百分比和粘度等级的增加会导致药物释放速率降低,并产生从仅几小时到24小时的广泛不同释放速率。

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