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Simple rapid validated RP-LC method for the estimation of flurbiprofen in rabbit serum and aqueous humor

机译:简单快速,快速验证的RP-LC方法评估兔血清和房水中的氟比洛芬

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摘要

New reversed-phase liquid chromatographic methods, with UV detection, were developed for the quantitative estimation of flurbiprofen in rabbit blood serum and aqueous humor. The mobile phase and other chromatographic conditions were optimized to minimize interference from biological matrix and at the same time provide sufficient sensitivity for the method to be adopted for in vivo studies of ophthalmic formulations of flurbiprofen. Acetonitrile was used to precipitate proteins from serum or aqueous humor during sample preparation. A mobile phase of methanol: acetonitrile: phosphate buffer pH 5.6 (40: 20: 40) was employed with UV detection at 248nm for estimation of drug in both the biological matrix. The retention time and asymmetry factor for the proposed method of estimation in serum and aqueous humor was found to be 3.1312 +/- 0.0101 min and 1.1310 +/- 0.0091 respectively. The linear regression equations obtained by least square regression method, were Area (mu Vsec) = 52.27 x Conc. (in ng/ml) - 1618.70 in serum and Area (mu Vsec) 61.79 x Conc. (in ng/ml) - 783.24 in aqueous humor. The results of analysis were treated statistically, as per ICH guidelines for validation of analytical procedures, USP-2003, and by recovery studies. The results were found to be accurate, reproducible and free from interference. The developed methods were further used for estimation of flurbiprofen in rabbit serum and aqueous humor following single topical administration of in-house aqueous drop and market formulation to rabbit eye.
机译:开发了具有紫外检测功能的新型反相液相色谱方法,用于定量评估兔血清和房水中的氟比洛芬。优化了流动相和其他色谱条件,以最大程度地减少对生物基质的干扰,同时为氟比洛芬眼科制剂的体内研究所采用的方法提供足够的灵敏度。在样品制备过程中,使用乙腈从血清或房水中沉淀蛋白质。使用甲醇:乙腈:磷酸盐缓冲液pH 5.6(40:20:40)的流动相,在248nm处进行UV检测,以评估两种生物基质中的药物。所提出的估计方法在血清和房水中的保留时间和不对称因子分别为3.1312 +/- 0.0101分钟和1.1310 +/- 0.0091。通过最小二乘回归法获得的线性回归方程为面积(mu Vsec)= 52.27 x Conc。 (ng / ml)-血清和面积(mu Vsec)为1618.70 x Conc。 (ng / ml)-783.24房水。根据ICH确认分析程序的准则,USP-2003和回收率研究,对分析结果进行统计学处理。发现结果是准确的,可重复的并且没有干扰。在对兔眼单次局部给药室内水剂和市售制剂后,将开发的方法进一步用于评估兔血清和房水中的氟比洛芬。

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