Yeung P K, Mosher S J, Klassen G A, McGilveray I J
College of Pharmacy, Dalhousie University, Halifax, Nova Scotia, Canada.
Ther Drug Monit. 1991 Jul;13(4):369-74. doi: 10.1097/00007691-199107000-00015.
Diltiazem (DTZ) is a calcium antagonist widely used in the treatment of angina and related heart diseases. It is extensively metabolized into a host of metabolites, some of which have potent pharmacological activities. Previous work has shown that DTZ and its major metabolite N-desmethyl-DTZ (MA) were unstable and readily decomposed to deacetyl-DTZ (M1) and deacetyl N-desmethyl-DTZ (M2), respectively. This report describes the stability of DTZ and its metabolites in plasma samples stored at -20 and -70 degrees C for different periods up to 12 weeks. The results indicate that in those samples obtained from volunteers who received DTZ, no deterioration of DTZ or MA occurred up to 8 weeks, but considerable deterioration of DTZ to M1 and MA to M2 (p less than 0.01) occurred after 12 weeks. However, in samples prepared by adding DTZ and its metabolites to outdated plasma (spiked plasma), deterioration of DTZ occurred after 4-6 weeks of storage, but there were no concomitant increases in concentrations of M1 or M2. Thus, it appears that decomposition of DTZ and MA was affected by the nature of the plasma materials, but the reason for the differences in analyte stability observed between volunteers' and spiked plasma is not known. Also, it appeared that DTZ and its metabolites in plasma samples stored at -70 degrees C may be more stable than those at -20 degrees C, although further studies are required to substantiate this observation. On the basis of these results, plasma samples obtained from patients or volunteers receiving DTZ should be analyzed within 8 weeks when the samples are stored frozen at -20 degrees C.
地尔硫䓬(DTZ)是一种广泛用于治疗心绞痛及相关心脏病的钙拮抗剂。它会广泛代谢为多种代谢产物,其中一些具有强大的药理活性。先前的研究表明,DTZ及其主要代谢产物N-去甲基-DTZ(MA)不稳定,容易分别分解为脱乙酰基-DTZ(M1)和脱乙酰基N-去甲基-DTZ(M2)。本报告描述了DTZ及其代谢产物在-20℃和-70℃下储存不同时间段(最长12周)的血浆样本中的稳定性。结果表明,在从接受DTZ的志愿者获得的那些样本中,在8周内DTZ或MA没有发生降解,但在12周后DTZ大量降解为M1,MA大量降解为M2(p<0.01)。然而,在通过将DTZ及其代谢产物添加到过期血浆(加标血浆)中制备的样本中,DTZ在储存4-6周后发生降解,但M1或M2的浓度没有随之增加。因此,似乎DTZ和MA的分解受到血浆材料性质的影响,但在志愿者血浆和加标血浆中观察到的分析物稳定性差异的原因尚不清楚。此外,虽然需要进一步研究来证实这一观察结果,但似乎储存在-70℃的血浆样本中的DTZ及其代谢产物可能比储存在-20℃的更稳定。基于这些结果,当样本在-20℃冷冻储存时,从接受DTZ的患者或志愿者获得的血浆样本应在8周内进行分析。