Eckstein J A, Swanson S P
Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.
J Chromatogr B Biomed Appl. 1995 Jun 9;668(1):153-8. doi: 10.1016/0378-4347(95)00058-q.
A method for the analysis of the AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate) receptor antagonist LY300164 (compound I) and its N-acetyl metabolite (compound II) in plasma was developed. The assay utilized solid-phase extraction on a C18 Bond Elut cartridge followed by reversed-phase HPLC with UV detection at 310 nm. The method exhibited a large linear range from 0.05 microgram/ml to 50 micrograms/ml with an intra-assay accuracy for compound I and compound II ranging from 89.0% to 114.5% and intra-assay precision ranging from 0.5 to 15.3% in mouse, rat, dog, and monkey plasma. The inter-assay accuracy of compound I and compound II was 93.3% to 101.8% and the inter-assay precision was 1.6% to 11.2% in dog plasma. The lower limit of quantitation was 0.05 microgram/ml for compound I in plasma from all species tested. The lower limit of quantitation for compound II was 0.05 microgram/ml in dog and monkey plasma and 0.1 microgram/ml in mouse and rat plasma. Extracts of compound I and II from dog plasma were shown to be stable for 24 h at room temperature, and both compounds were stable when spiked into rat and monkey plasma frozen at -70 degrees C for 27 days. The method has shown to be useful in the investigation of the pharmacokinetics of the parent compound (I) and metabolite (II) in preclinical studies.
建立了一种分析血浆中AMPA(α-氨基-3-羟基-5-甲基-4-异恶唑丙酸)受体拮抗剂LY300164(化合物I)及其N-乙酰代谢物(化合物II)的方法。该测定采用C18 Bond Elut柱进行固相萃取,然后进行反相高效液相色谱,在310 nm处进行紫外检测。该方法在0.05微克/毫升至50微克/毫升范围内具有较大的线性范围,化合物I和化合物II在小鼠、大鼠、狗和猴血浆中的批内准确度为89.0%至114.5%,批内精密度为0.5%至15.3%。化合物I和化合物II在狗血浆中的批间准确度为93.3%至101.8%,批间精密度为1.6%至11.2%。在所有测试物种的血浆中,化合物I的定量下限为0.05微克/毫升。化合物II在狗和猴血浆中的定量下限为0.05微克/毫升,在小鼠和大鼠血浆中的定量下限为0.1微克/毫升。狗血浆中化合物I和II的提取物在室温下可稳定24小时,当将这两种化合物加入到-70℃冷冻的大鼠和猴血浆中时,它们在27天内都保持稳定。该方法已证明在临床前研究中对母体化合物(I)和代谢物(II)的药代动力学研究有用。