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通过分光光度法对美洛昔康片剂剂型进行溶出度研究及定量分析。

Dissolution studies and quantification of meloxicam in tablet dosage form by spectrophotometry.

作者信息

Induri Madhusudhanareddy, Mantripragada Bhagavan Raju, Yejella Rajendra Prasad, Kunda Pavankumar Reddy, Nannapaneni Dharma Theja, Boddu Rajkumar

机构信息

Department of Pharmaceutical Chemistry, Malla Reddy College of Pharmacy, Secunderabad, Andhra Pradesh, India.

出版信息

Pak J Pharm Sci. 2012 Jan;25(1):283-7.

Abstract

Two simple and inexpensive UV spectrophotometric methods were developed for the quantification and dissolution studies of meloxicam in tablet dosage forms. Meloxicam was estimated at 365nm and 360nm in Method I and Method II, respectively. The calibration curve was linear over a concentration range from 2.0 to 12.0μg/ml for both methods. The limit of detection and limit of quantitation were found to be 0.12μg/ml and 0.38μg/ml, 0.09μg/ml and 0.27μg/ml for Method I and Method II, respectively. The percentage recoveries of meloxicam were found to be 99.68 to 100.61% and 99.11 to 100.96% for Method I and Method II, respectively. It was concluded that the developed methods are precise, accurate and were successfully applied for the estimation of meloxicam in pharmaceutical formulations and in vitro dissolution studies.

摘要

开发了两种简单且成本低廉的紫外分光光度法,用于美洛昔康片剂剂型的定量和溶出度研究。在方法I和方法II中,分别于365nm和360nm处测定美洛昔康。两种方法的校准曲线在2.0至12.0μg/ml的浓度范围内均呈线性。方法I的检测限和定量限分别为0.12μg/ml和0.38μg/ml,方法II的检测限和定量限分别为0.09μg/ml和0.27μg/ml。方法I和美洛昔康的回收率分别为99.68%至100.61%和99.11%至100.96%。结论是,所开发的方法精确、准确,并成功应用于药物制剂中美洛昔康的测定和体外溶出度研究。

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