Miller R B, Dadgar D, Lalande M
Analytical Research Center, L.A.B. Bio-Research International Inc., Senneville, Montreal, Quebec, Canada.
J Chromatogr. 1993 May 5;614(2):293-8. doi: 10.1016/0378-4347(93)80321-t.
A sensitive, accurate, and reproducible high-performance liquid chromatographic procedure for the analysis of indapamide in human whole blood is reported. After a single-step liquid-liquid extraction at pH 6.6 using diethyl ether, indapamide was eluted from a Nucleosil C18 5-microns column with 80 mM ammonium acetate, pH 3.5-acetonitrile-2-propanol (65:30:5, v/v/v). The peak height versus whole blood concentration was linear over the range 10.0-500 ng/ml using ultraviolet detection. The mean absolute recovery of indapamide using the described assay was 87.4%. The inter- and intra-day accuracy and precision were within 9.6% of the actual values for all concentrations investigated. Furthermore, this procedure was applied to the analysis of whole blood samples from healthy subjects receiving a single 2.5-mg oral dose of indapamide.
报道了一种灵敏、准确且可重现的高效液相色谱法,用于分析人全血中的吲达帕胺。在pH 6.6条件下用乙醚进行单步液-液萃取后,吲达帕胺用80 mM乙酸铵(pH 3.5)-乙腈-2-丙醇(65:30:5,v/v/v)从Nucleosil C18 5微米柱上洗脱。使用紫外检测时,峰高与全血浓度在10.0 - 500 ng/ml范围内呈线性关系。使用所述测定法时,吲达帕胺的平均绝对回收率为87.4%。对于所有研究浓度,日间和日内准确度及精密度在实际值的9.6%以内。此外,该方法应用于分析接受2.5 mg吲达帕胺单次口服剂量的健康受试者的全血样本。