Jalbani Nida S, Solangi Amber R, Khuhawar Muhammad Yar, Memon Shahabuddin, Junejo Ranjhan, Memon Ayaz Ali
University of Sindh National Center of Excellence in Analytical Chemistry, Jamshoro, Pakistan.
University of Sindh Institute of Advanced Research Studies in Chemical Sciences, Jamshoro, Pakistan.
Turk J Pharm Sci. 2020 Oct;17(5):465-473. doi: 10.4274/tjps.galenos.2019.42243. Epub 2020 Oct 30.
Non-steroidal anti-inflammatory drugs (NSAIDs) are widely used for the treatment of acute to chronic pain. A simple, fast, and reliable gas chromatographic (GC) method with flame ionization detection has been developed for the determination of NSAIDs such as diclofenac sodium, ibuprofen, and mefenamic acid after derivatization with ethyl chloroformate.
The GC conditions were optimized as elution from a DB-1 column (30 mx0.32 mm id) at column temperature 150 °C for 3 min, followed by a heating rate of 20 °C/min up to 280 °C and a hold time of 5 min. The nitrogen flow rate was 2.5 mL/min. For spectrophotometric studies, the absorbance was measured against methanol at a wavelength of 200-500 nm.
The calibration curves were linear within 2-10 μg/mL with limits of detection of 0.4-0.6 μg/mL of each drug. The derivatization elution, separation, and quantitation were repeatable (n=3) with relative standard deviation (RSD) within 3.9%. The method was applied for the analysis of the drugs from pharmaceutical formulations and the results of the analysis agreed with labeled values with RSDs within 0.5-3.9%. The results were also confirmed by standard addition method. The percent recovery was calculated with spiked deproteinized human blood serum and urine samples and % recovery of the drugs was obtained within 96-98% with RSDs within 3.1%.
The validated method proved its ability for the assay of NSAIDs in bulk and dosage form in a short analysis time. The method was also useful for the analysis of biological samples.
非甾体抗炎药(NSAIDs)广泛用于治疗急性至慢性疼痛。已开发出一种简单、快速且可靠的带有火焰离子化检测的气相色谱(GC)方法,用于测定经氯甲酸乙酯衍生化后的双氯芬酸钠、布洛芬和甲芬那酸等NSAIDs。
GC条件优化为:在DB - 1柱(30 m×0.32 mm内径)上,柱温150°C保持3分钟,然后以20°C/分钟的升温速率升至280°C并保持5分钟。氮气流量为2.5 mL/分钟。对于分光光度研究,在200 - 500 nm波长下以甲醇为参比测量吸光度。
校准曲线在2 - 10 μg/mL范围内呈线性,每种药物的检测限为0.4 - 0.6 μg/mL。衍生化洗脱、分离和定量具有可重复性(n = 3),相对标准偏差(RSD)在3.9%以内。该方法用于分析药物制剂中的药物,分析结果与标示值相符,RSD在0.5 - 3.9%以内。结果也通过标准加入法得到证实。用加标的脱蛋白人血清和尿液样品计算回收率,药物回收率在96 - 98%之间,RSD在3.1%以内。
经验证的方法证明了其在短分析时间内测定原料药和剂型中NSAIDs的能力。该方法也可用于生物样品的分析。