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Formulation and evaluation of sustained released buccoadhesive tablets of Itraconazole

机译:碘康唑持续释放的Bucocoghy粘附片的制剂和评价

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The aim of present research was to report the buccoadhesive tablet of itraconazole to provide localized delivery of drug for the treatment of oral thrush and maintain the drug concentration in the mouth for prolonged period of time thereby improving the oral bioavailability of drug. Buccoadhesive tablet is a sustained release of itraconazole for easy permeation across buccal mucosa and provide a local delivery concentration that may or may not be sufficient to maintain MIC to kill the microorganism. Solid dispersion of itraconazole was prepared by solvent evaporation technique using silica gel act as adsorbent and drug was soluble in chloroform to obtain a slurry or uniform mixture. The buccoadhesive tablet was prepared by direct compression method using different polymers such as Carbopol(C934P),HPMC K4M, Eudragit E100. Five formulations of different concentrations were prepared. Itraconazole strength were kept constant at 30mg and target was fixed at 120mg. After examine the moisture content, bulk density, tapped density, Angle of repose of powder blend get the result were found to be prescribed limit and indicated good flow property. Then the tablets were evaluated for hardness, thickness, weight variation, drug content, friability, swelling index, In-vitro drug release.
机译:目前研究的目的是报告伊唑康唑的Buccoadgesive片剂,为治疗口腔鹅口疮的药物提供局部递送,并使口腔中的药物浓度长时间,从而提高药物的口服生物利用度。 Buccoadghersive平板电脑是伊丙酮的持续释放,以便在颊粘膜上轻松渗透,并提供可能或可能不足以维持MIC以杀死微生物的局部递送浓度。通过硅胶溶剂蒸发技术制备伊唑康唑的固体分散体,用硅胶作用作为吸附剂和药物可溶于氯仿,得到浆料或均匀的混合物。通过使用不同的聚合物如Carbopol(C934P),HPMC K4M,Eudragit E100,通过直接压缩方法制备BucoCoadghable片剂。制备了五种不同浓度的制剂。在30mg的30mg下保持伊丙酮强度恒定,并在120mg下固定靶标。在检查水分含量,散装密度,敲击密度,粉末混合物的休息角得到结果被发现是规定的极限,并表明良好的流动性。然后评价片剂的硬度,厚度,重量变异,药物含量,脆性,溶胀指数,体外药物释放。

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