Control of Drug Dissolution Rate from Film Dosage Forms Containing Valsartan.

International Scholarly Research Notices Pub Date : 2016-05-23 eCollection Date: 2016-01-01 DOI:10.1155/2016/5135173
Yoshifumi Murata, Kyoko Kofuji, Chieko Maida
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引用次数: 5

Abstract

Film dosage forms (FDs) containing valsartan (VST), a popular antihypertensive drug, were prepared using a casting method with sodium alginate and other polysaccharides as the film base. Drug dissolution profiles of the FDs were investigated in limited medium. The FDs were 170-200 μm thick and were easy to handle. All FDs immediately swelled and disintegrated in the medium. About 23% of the VST incorporated into the FD prepared with 1.5% sodium alginate dissolved at 5 min. The initial dissolution rate of VST increased upon the addition of chitosan to the film base; this effect was not observed in the case of chitin. On the other hand, the rate apparently decreased upon modification with alginic acid. In addition, the solubility of VST in the dissolution medium was changed by the addition of chitosan or alginic acid. FDs prepared with polysaccharides are useful for simplifying the administration of drugs to patients, and the drug dissolution rate from FDs can be controlled by modification.

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含缬沙坦薄膜剂型药物溶出度的控制。
以海藻酸钠和其他多糖为膜基,采用铸造法制备了缬沙坦(VST)薄膜剂型。研究了FDs在有限介质中的药物溶出谱。fd厚度为170 ~ 200 μm,易于操作。所有fd立即膨胀并在介质中分解。约23%的VST纳入FD, 1.5%海藻酸钠溶解5分钟。壳聚糖加入膜基后,VST的初始溶解速率增加;这种效果在几丁质中没有观察到。另一方面,褐藻酸修饰后,反应速率明显降低。此外,壳聚糖或海藻酸的加入改变了VST在溶解介质中的溶解度。用多糖制备的体外溶出剂有助于简化患者给药,而且体外溶出剂的溶出率可以通过修饰来控制。
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