混合水增溶法测定原料药及其剂型中美洛昔康的新型生态友好分光光度法

Sreenath R, Remi S L
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引用次数: 0

摘要

溶解度是评价难溶性药物的关键因素。文献调查表明,难溶性药物的分光光度法测定多采用有机溶剂。有机溶剂的缺点是成本高、毒性大、污染大、挥发性差。亲水增溶方法涉及通过添加亲水剂来增加难溶性药物在水中的溶解度。大多数非甾体抗炎药,如美洛昔康,甲氧芬酸,乙酰氯芬酸,都难溶于水。结果表明,美洛昔康可溶于10%苯甲酸钠和10%辛酸钠的混合溶液中,吸光度在364nm处最大。该方法在2 ~ 10µg/ml范围内呈线性,相关系数(R2)为0.9968。该方法的定量限和定量限分别为0.2634µg/ml和0.7983µg/ml。以10%苯甲酸钠和10%辛酸钠为亲水剂,建立了一种简便、安全、灵敏、经济的美洛昔康分光光度测定方法。该增溶方法可用于排除使用有机溶剂来估计难溶性药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Ecofriendly Novel Spectrophotometric Estimation and Validation of Meloxicam in Bulk Drug and their Dosage Form by mixed Hydrotropic Solubilization Method
Solubility is a crucial factor during estimation of poorly soluble drugs. Literature survey reveals spectrophotometric estimation of poorly soluble drugs are mostly done by employing organic solvents. The drawbacks of organic solvents include higher cost, toxicity, pollution and error due to volatility. Hydrotropic solubilisation method involves increasing the solubility of a poorly soluble drug in water with the addition of hydrotropic agents. Most of NSAIDs like Meloxicam, Mefenamic acid, Aceclofenacetc are poorly soluble in water. Meloxicam was found to be soluble in mixed hydrotropic solution of 10% sodium benzoate and 10% sodium caprylate with maximum absorbance at 364 nm. The developed method was found to be linear in the range of 2-10 µg/ml with correlation coefficient (R2) of 0.9968. The LOD and LOQ of proposed method was found to be 0.2634 µg/ml and 0.7983 µg/ml respectively. A novel, simple, safe, sensitive and cost-effective spectrophotometric estimation method was developed for estimation of Meloxicam using 10% sodium benzoate and 10% sodium caprylate as hydrotropic agent. This solubilization method can be employed to preclude the use of organic solvents for the estimation of poorly soluble drugs.
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