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采用加权回归法快速灵敏地反相高效液相色谱法测定药品中的酮咯酸

Rapid and Sensitive Reverse-phase High-performance Liquid Chromatography Method for Estimation of Ketorolac in Pharmaceuticals Using Weighted Regression.

作者信息

Dubey S K, Duddelly S, Jangala H, Saha R N

机构信息

Department of Pharmacy, Birla Institute of Technology and Science, Pilani 333 031, India.

出版信息

Indian J Pharm Sci. 2013 Jan;75(1):89-93. doi: 10.4103/0250-474X.113535.

Abstract

A reliable, rapid and sensitive isocratic reverse phase high-performance liquid chromatography method has been developed and validated for assay of ketorolac tromethamine in tablets and ophthalmic dosage forms using diclofenac sodium as an internal standard. An isocratic separation of ketorolac tromethamine was achieved on Oyster BDS (150×4.6 mm i.d., 5 μm particle size) column using mobile phase of methanol:acetonitrile:sodium dihydrogen phosphate (20 mM; pH 5.5) (50:10:40, %v/v) at a flow rate of 1.0 ml/min. The eluents were monitored at 322 nm for ketorolac and at 282 nm for diclofenac sodium with a photodiode array detector. The retention times of ketorolac and diclofenac sodium were found to be 1.9 min and 4.6 min, respectively. Response was a linear function of drug concentration in the range of 0.01-15 μg/ml (R (2)=0.994; linear regression model using weighing factor 1/x (2)) with a limit of detection and quantification of 0.002 μg/ml and 0.007 μg/ml, respectively. The % recovery and % relative standard deviation values indicated the method was accurate and precise.

摘要

已开发并验证了一种可靠、快速且灵敏的等度反相高效液相色谱法,以双氯芬酸钠为内标物,用于测定片剂和眼用剂型中的酮咯酸氨丁三醇。在Oyster BDS(内径150×4.6 mm,粒径5μm)柱上,以甲醇:乙腈:磷酸二氢钠(20 mM;pH 5.5)(50:10:40,%v/v)为流动相,流速为1.0 ml/min,实现了酮咯酸氨丁三醇的等度分离。使用光电二极管阵列检测器,在322 nm处监测酮咯酸的洗脱液,在282 nm处监测双氯芬酸钠的洗脱液。发现酮咯酸和双氯芬酸钠的保留时间分别为1.9分钟和4.6分钟。在0.01 - 15μg/ml范围内,响应是药物浓度的线性函数(R(2)=0.994;使用加权因子1/x(2)的线性回归模型),检测限和定量限分别为0.002μg/ml和0.007μg/ml。回收率和相对标准偏差百分比值表明该方法准确且精密。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c48e/3719155/2a8b4d56d62d/IJPhS-75-89-g001.jpg

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