首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Simultaneous determination of nine model compounds in permeability samples using RP-HPLC: Application to prove the cassette administration principle in single pass intestinal perfusion study in rats
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Simultaneous determination of nine model compounds in permeability samples using RP-HPLC: Application to prove the cassette administration principle in single pass intestinal perfusion study in rats

机译:RP-HPLC同时测定通透性样品中的9种模型化合物:在大鼠单次肠道灌注研究中证明盒式给药原理的应用

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摘要

A simple, sensitive and specific reversed phase high performance liquid chromatographic (RP-HPLC) method for simultaneous determination of atenolol, paracetamol, hydrochlorothiazide, caffeine, cephalexin, metoprolol, propranolol, ketoprofen along with phenol red (a non-absorbable compound) in samples obtained from intestinal in situ single-pass perfusion studies, was developed and validated. Chromatography was carried out on RP18 column with mobile phase comprising of 10mM phosphate buffer (pH 2.5) and methanol in gradient mode. The calibration curves were linear for all nine permeability model compounds (r 20.999) across the concentration range of 1.25-40μg/ml. The coefficient of variation for intra and inter-day assay precision was between 0.04 and 3.08% and the accuracy was between 98.39 and 109.45%. Stability studies were carried out at different storage conditions and all the analytes were found to be stable. The method was successfully applied for analysing the permeability samples obtained from in situ single pass perfusion studies. The effective permeability (P eff) values obtained upon cassette administration were in close proximity to the permeability values obtained upon single administration of model compounds. In conclusion, the developed RP-HPLC method can be used for high throughput cassette validation of rat in situ perfusion model for intestinal permeability assessment.
机译:一种简单,灵敏,特异的反相高效液相色谱(RP-HPLC)方法,可同时测定样品中的阿替洛尔,扑热息痛,氢氯噻嗪,咖啡因,头孢氨苄,美托洛尔,普萘洛尔,酮洛芬以及酚红(一种不可吸收的化合物)从肠道原位单次灌流研究中获得的结果已得到开发和验证。在RP18色谱柱上进行色谱分离,流动相包括10mM磷酸盐缓冲液(pH 2.5)和甲醇(梯度模式)。在1.25-40μg/ ml的浓度范围内,所有九种渗透性模型化合物(r 2> 0.999)的校准曲线均为线性。日内和日间分析精度的变异系数在0.04至3.08%之间,准确度在98.39至109.45%之间。在不同的储存条件下进行了稳定性研究,发现所有分析物都是稳定的。该方法成功地用于分析从原位单程灌注研究获得的渗透率样品。盒施用后获得的有效渗透率(P eff)值与单次施用模型化合物时获得的渗透率值非常接近。总之,开发的RP-HPLC方法可用于大鼠原位灌注模型的高通量盒验证,以评估肠道通透性。

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