Läer S, Scholz H, Uebeler P, Neumann J, Zimmermann N
Abteilung Allgemeine Pharmakologie, Universitäts-Krankenhaus Eppendorf, Hamburg, Germany.
J Chromatogr Sci. 1997 Mar;35(3):93-6. doi: 10.1093/chromsci/35.3.93.
A new high-performance liquid chromatographic method has been developed for the determination of diltiazem in human cardiac tissue. Tissue samples are homogenized and digested with trypsin solution. Diltiazem and the internal standard are extracted with acetone. The extract is evaporated to dryness and reconstituted in potassium phosphate buffer. Samples are then cleaned up with solid-phase extraction columns. Diltiazem and the internal standard show recoveries of 59% +/- 16 and 52% +/- 13. The linearity range is 0.12-2.25 ng/mg wet weight. The limit of quantitation is 0.12 ng/mg (w/w). The percentage coefficient of variation of intra-assay varies between 3.57 and 11.2, and that of interassay varies between 5.42 and 11.7. As an application of the assay, a diltiazem cardiac tissue level in a patient on oral therapy for supraventricular tachycardia is reported.
已开发出一种新型高效液相色谱法用于测定人体心脏组织中的地尔硫䓬。将组织样品匀浆并用胰蛋白酶溶液消化。用地尔硫䓬和内标物用丙酮萃取。提取物蒸发至干,并用磷酸钾缓冲液复溶。然后用固相萃取柱对样品进行净化。地尔硫䓬和内标物的回收率分别为59%±16和52%±13。线性范围为0.12 - 2.25 ng/mg湿重。定量限为0.12 ng/mg(w/w)。批内变异系数百分比在3.57至11.2之间,批间变异系数百分比在5.42至11.7之间。作为该测定法的应用,报告了一名接受口服治疗室上性心动过速患者的地尔硫䓬心脏组织水平。