Department of Drug Discovery and Biomedical Sciences, Medical University of South Carolina, Charleston, South Carolina
Department of Drug Discovery and Biomedical Sciences, Medical University of South Carolina, Charleston, South Carolina.
Drug Metab Dispos. 2019 Jul;47(7):764-767. doi: 10.1124/dmd.119.087189. Epub 2019 Apr 26.
A tenable hypothesis is presented which explains disparities between older oral dl-MPH bioavailability data generated using chiral derivatization-gas chromatography versus more recent findings using chiral liquid chromatography. These disparities persist in current literature. The gas chromatographic methods found that the absolute bioavailability of d-MPH is 23% and that of l-MPH is 5% (i.e., 82% as the active d-isomer), while liquid chromatographic methods consistently report that approximately 99% of circulating MPH is d-MPH. Older methods used perfluoroacylated S-prolyl derivatizing agents which have a history of imprecision due to the susceptibility of the prolyl S-configuration to isomerize to the R-enantiomer. Accordingly, any R-prolyl impurity in the chiral derivatization reagent yields the (R,R,R)-MPH-prolyl diastereomer which, in being related as the opposite enantiomer of (S,S,S)-prolyl-MPH, co-elutes with l-(S,S)-MPH. This results in overestimation of the percent l-MPH at the expense of underestimating d-MPH. Unless compelling reasons exist to justify use of any chiral discriminators, less complex and less costly achiral analysis of plasma MPH appears appropriate for d-MPH quantitation since 99% exists as d-MPH. However, simultaneous plasma monitoring of d-MPH and l-MPH may be warranted when alterations in first-pass hepatic metabolism by carboxylesterase 1 (CES1) occurs. For example, (a) with transdermal dl-MPH delivery; (b) in cases of concomitant dl-MPH and a CES1 inhibitor, e.g., ethanol, which elevates l-MPH and d-MPH concentrations; (d) in forensic studies of intravenous or intranasal dl-MPH abuse; (e) were dl-MPH to be formulated as a free base sublingual product; or (f) as emerging advances in dl-MPH gene-dose effects warrant isomer correlations.
提出了一个可行的假设,解释了使用手性衍生化-气相色谱法生成的老年口服 dl-MPH 生物利用度数据与使用手性液相色谱法获得的最近发现之间的差异。这些差异在当前文献中仍然存在。气相色谱法发现,d-MPH 的绝对生物利用度为 23%,l-MPH 的生物利用度为 5%(即活性 d-对映体为 82%),而液相色谱法一致报告说,大约 99%的循环 MPH 为 d-MPH。较旧的方法使用全氟酰化 S-脯氨酸衍生化试剂,由于脯氨酸 S-构型易于异构化为 R-对映体,因此这些试剂的历史上存在不准确性。因此,手性衍生化试剂中的任何 R-脯氨酸杂质都会产生(R,R,R)-MPH-脯氨酸非对映异构体,与 l-(S,S)-MPH 相关,与 l-(S,S)-MPH 共洗脱。这导致 l-MPH 的百分比高估,而 d-MPH 的百分比低估。除非有令人信服的理由证明使用任何手性鉴别器是合理的,否则对于 d-MPH 定量,使用不太复杂和成本较低的非手性分析血浆 MPH 似乎更为合适,因为 99%的 MPH 以 d-MPH 形式存在。然而,当羧基酯酶 1(CES1)发生首过肝代谢改变时,可能需要同时监测血浆中的 d-MPH 和 l-MPH。例如,(a) 经皮 dl-MPH 给药;(b) 在 dl-MPH 和 CES1 抑制剂同时存在的情况下,例如乙醇,可升高 l-MPH 和 d-MPH 浓度;(d) 在静脉内或鼻内滥用 dl-MPH 的法医研究中;(e) dl-MPH 被制成游离碱舌下产品;或 (f) 随着 dl-MPH 基因剂量效应的新进展需要对映体相关性。