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反相高效液相色谱法同时测定帕博西尼和来曲唑的优化和验证。

Optimization and validation of RP-HPLC method for simultaneous estimation of palbociclib and letrozole.

机构信息

a Rajarambapu College of Pharmacy , Sangli , India.

b Rajarambapu College of Pharmacy, Pharmaceutical Chemistry , Sangli , India.

出版信息

Toxicol Mech Methods. 2018 Mar;28(3):187-194. doi: 10.1080/15376516.2017.1388458. Epub 2017 Nov 3.

Abstract

A simple, rapid, and robust RP-HPLC method have been developed and validated to measure palbociclib (PB) and letrozole (LT) at single wavelength (254 nm). A isocratic elution of samples performed on Intersil C (4.6 mm × 250 mm particle size 5 μm) column with mobile phase consisting 0.02 M sodium dihydrogen phosphate buffer (pH 5.5): acetonitrile: methanol (80:10:10 v/v/v) delivered at flow rate 1.0 mL min. A good linear response was achieved over the range of 5-50 μg mL. The LODs for PB and LT were found to be 0.098 and 0.0821 µg mL, while the LOQs for PB and LT were 0.381-0.315 µg mL, respectively. The method was quantitatively evaluated in terms of system suitability test, linearity, precision, accuracy (recovery) and robustness as per standard guidelines. The method is simple, convenient and suitable for the analysis of PB and LT in bulk drug.

摘要

建立并验证了一种简单、快速、可靠的反相高效液相色谱法,用于在单波长(254nm)下测定帕博西尼(PB)和来曲唑(LT)。样品在 Intersil C(4.6mm×250mm,粒径 5μm)柱上进行等度洗脱,流动相由 0.02M 磷酸二氢钠缓冲液(pH5.5):乙腈:甲醇(80:10:10 v/v/v)组成,流速为 1.0mL/min。在 5-50μg/mL 范围内,获得了良好的线性响应。PB 和 LT 的检出限分别为 0.098 和 0.0821μg/mL,定量限分别为 0.381-0.315μg/mL。该方法按照标准指南,从系统适用性试验、线性、精密度、准确度(回收率)和耐用性等方面进行了定量评估。该方法简单、方便,适用于原料药中 PB 和 LT 的分析。

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