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生物样品中盐酸劳卡尼及其三种主要代谢物的气相色谱同步测定。

Simultaneous gas chromatographic determination of lorcainide hydrochloride and three of its principal metabolites in biological samples.

作者信息

Woestenborghs R, Michiels M, Heykants J

出版信息

J Chromatogr. 1979 Oct 11;164(2):169-76. doi: 10.1016/s0378-4347(00)81185-8.

DOI:10.1016/s0378-4347(00)81185-8
PMID:541407
Abstract

A method is described for the determination of the antiarrhythmic drug lorcainide hydrochloride and its three main metabolites in plasma, urine, faeces and tissues from man and animals. The procedure involves the extract of the parent drug, its metabolites and the internal standard from the biological materials at different alkaline pH values, back-extraction into sulphuric acid and re-extraction into the organic phase (heptane--isoamyl alcohol). After silylation of the different phenolic and the N-dealkylated metabolites, analyses were carried out by automated gas--liquid chromatography with electron-capture detection. The method has a sensitivity limit of 5 ng for lorcainide, and 10--20 ng for the various metabolites, per millilitre of plasma. The method was applied to urine, faeces, plasma and tissue samples from man and animals. It was also suitable for automatic sample analysis.

摘要

本文描述了一种测定人及动物血浆、尿液、粪便和组织中抗心律失常药物盐酸劳卡尼及其三种主要代谢物的方法。该方法包括在不同碱性pH值下从生物材料中提取母体药物、其代谢物和内标,反萃取到硫酸中,再萃取到有机相(庚烷 - 异戊醇)。对不同的酚类和N - 去烷基化代谢物进行硅烷化后,采用带电子捕获检测的自动气液色谱法进行分析。该方法对血浆中劳卡尼的检测限为每毫升5纳克,对各种代谢物的检测限为10 - 20纳克。该方法应用于人及动物的尿液、粪便、血浆和组织样本。它也适用于自动样品分析。

相似文献

1
Simultaneous gas chromatographic determination of lorcainide hydrochloride and three of its principal metabolites in biological samples.生物样品中盐酸劳卡尼及其三种主要代谢物的气相色谱同步测定。
J Chromatogr. 1979 Oct 11;164(2):169-76. doi: 10.1016/s0378-4347(00)81185-8.
2
Mass spectral investigation of the metabolites of lorcainide in man.人体中劳卡尼代谢物的质谱研究。
Eur J Drug Metab Pharmacokinet. 1983 Oct-Dec;8(4):351-62. doi: 10.1007/BF03188767.
3
The use and limitations of deuterated lorcainide in metabolism and pharmacokinetic studies.氘代劳卡尼在代谢和药代动力学研究中的应用及局限性
Biomed Mass Spectrom. 1985 Jan;12(1):38-42. doi: 10.1002/bms.1200120108.
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The pharmacokinetics and tissue distribution of the new antiarrhythmic agent lorcainide (R 15889) in rats.新型抗心律失常药物劳卡尼(R 15889)在大鼠体内的药代动力学及组织分布
Arzneimittelforschung. 1980;30(4):619-21.
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Excretion and metabolism of lorcainide in rats, dogs and man.劳卡尼在大鼠、狗和人体内的排泄与代谢。
Eur J Drug Metab Pharmacokinet. 1983 Oct-Dec;8(4):335-49. doi: 10.1007/BF03188766.
6
[HPLC method for determination of lorcainide hydrochloride in human serum].高效液相色谱法测定人血清中盐酸劳卡尼
Yao Xue Xue Bao. 1995;30(8):605-9.
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Sensitive gas chromatographic method for the determination of cinnarizine and flunarizine in biological samples.
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Quantitation of flecainide acetate, a new antiarrhythmic agent, in biological fluids by gas chromatography with electron-capture detection.用带电子捕获检测的气相色谱法定量生物流体中的新型抗心律失常药醋酸氟卡尼。
J Pharm Sci. 1984 Oct;73(10):1469-71. doi: 10.1002/jps.2600731037.
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Pharmacodynamics of the initiation of antiarrhythmic therapy with lorcainide.
Am J Cardiol. 1984 Feb 1;53(4):544-51. doi: 10.1016/0002-9149(84)90028-6.
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Pharmacokinetics of lorcainide, a new antiarrhythmic drug, in patients with cardiac rhythm disorders.
Am J Cardiol. 1981 Jul;48(1):157-63. doi: 10.1016/0002-9149(81)90585-3.

引用本文的文献

1
Bioavailability and saturation of the presystemic metabolism of oral lorcainide therapy initiated in three different dose regimens.在三种不同剂量方案下开始口服劳卡尼治疗时的生物利用度及首过代谢的饱和度。
Eur J Clin Pharmacol. 1983;24(4):517-9. doi: 10.1007/BF00609895.
2
Excretion and metabolism of lorcainide in rats, dogs and man.劳卡尼在大鼠、狗和人体内的排泄与代谢。
Eur J Drug Metab Pharmacokinet. 1983 Oct-Dec;8(4):335-49. doi: 10.1007/BF03188766.
3
Clinical pharmacokinetics of the newer antiarrhythmic agents.新型抗心律失常药物的临床药代动力学
Clin Pharmacokinet. 1984 Sep-Oct;9(5):375-403. doi: 10.2165/00003088-198409050-00001.