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Combined gas chromatographic-mass spectrometric procedure for the measurement of captopril and sulfur-conjugated metabolites of captopril in plasma and urine.

作者信息

Drummer O H, Jarrott B, Louis W J

出版信息

J Chromatogr. 1984 Jan 13;305(1):83-93. doi: 10.1016/s0378-4347(00)83316-2.

DOI:10.1016/s0378-4347(00)83316-2
PMID:6368577
Abstract

A gas chromatographic-mass spectrometric method is described for the simultaneous measurement of the novel anti-hypertensive drug captopril, and the following metabolites: captopril disulfide dimer, S-methyl captopril, and S-methyl captopril sulfone. With this method all derivatives can be chromatographed using conventional gas chromatography of hexafluoroisopropyl esters in one temperature-programmed run and these can then be quantitated using selected-ion monitoring techniques. Using urine or plasma, captopril, S-methyl captopril and the disulfide dimer of captopril in concentrations as low as 1 ng/ml, 10 ng/ml and 25 ng/ml, respectively can be detected. The reproducibility of the method is satisfactory both within-assay and inter-assay. This technique has demonstrated that the pattern of urinary excretion of these compounds in both man and rat was similar. Excretion of unchanged captopril, S-methyl captopril and the disulfide dimer over 6 h in man given captopril (50 or 100 mg) chronically was 18.3%, 0.97% and 3.06%, respectively. Corresponding excretion of these three compounds in the rat following a single 10 mg/kg dose was 18.3%, 2.69% and 1.8%, respectively. A possible sulfone oxidation product of S-methyl captopril was not detected in the urine of either man or rat.

摘要

相似文献

1
Combined gas chromatographic-mass spectrometric procedure for the measurement of captopril and sulfur-conjugated metabolites of captopril in plasma and urine.
J Chromatogr. 1984 Jan 13;305(1):83-93. doi: 10.1016/s0378-4347(00)83316-2.
2
Quantitative determination of captopril in blood and captopril and its disulfide metabolites in plasma by gas chromatography.
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Determination of captopril in human blood and urine by GLC-selected ion monitoring mass spectrometry after oral coadministration with its isotopomer.口服卡托普利及其同位素异构体后,通过气相色谱-选择离子监测质谱法测定人血液和尿液中的卡托普利。
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Identification and determination of the S-methyl metabolite of captopril in human plasma by selected-ion monitoring gas chromatography-mass spectrometry.采用选择离子监测气相色谱-质谱法鉴定和测定人血浆中卡托普利的S-甲基代谢物。
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Effect of probenecid on the disposition of captopril and captopril dimer in the rat.丙磺舒对大鼠体内卡托普利及其二聚体处置的影响。
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Biochem Pharmacol. 1983 May 15;32(10):1563-8. doi: 10.1016/0006-2952(83)90328-3.

引用本文的文献

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Pharmacokinetics of captopril in healthy subjects and in patients with cardiovascular diseases.卡托普利在健康受试者和心血管疾病患者中的药代动力学。
Clin Pharmacokinet. 1988 Apr;14(4):241-59. doi: 10.2165/00003088-198814040-00002.
2
Captopril. An update of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in hypertension and congestive heart failure.卡托普利。其药效学和药代动力学特性的最新进展,以及在高血压和充血性心力衰竭中的治疗应用。
Drugs. 1988 Nov;36(5):540-600. doi: 10.2165/00003495-198836050-00003.
3
Clinical pharmacokinetics of the newer ACE inhibitors. A review.
新型血管紧张素转换酶抑制剂的临床药代动力学。综述。
Clin Pharmacokinet. 1990 Sep;19(3):177-96. doi: 10.2165/00003088-199019030-00003.