New high-performance liquid chromatographic method for plasma/serum analysis of lamotrigine

被引:38
作者
Croci, D [1 ]
Salmaggi, A [1 ]
de Grazia, U [1 ]
Bernardi, G [1 ]
机构
[1] Ist Neurochirurg C Besta, Analyt Clinicopharmacol Lab, I-20133 Milan, Italy
关键词
lamotrigine; high-performance liquid chromatography; without extraction;
D O I
10.1097/00007691-200112000-00012
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Lamotrigine is an anticonvulsant drug recently approved in Italy for clinical use. Therapeutic monitoring of lamotrigine is relevant for patient management and avoidance of toxicity. The authors describe a simple, sensitive, and highly selective high-performance liquid chromatography method that does not involved extraction for analysis of serum lamotrigine. Serum (20 muL) with internal standard (BW 725 C) was injected directly into a column (25 cm x 4.6 mm) with an internal surface reversed phase (ISRP). The mobile phase consisted of 0.01 mol/L potassium phosphate bibasic (pH 6.0) and acetonitrile (82:18), the flow rate was 1.0 mL/min, and UV detection was optimized at 330 nm. The overall between-run coefficient of variance ranged from 1.89% to 3.25% and the lowest limit of detection was 0.05 mg/L. High linearity (r = 0.9996) in a wide range of concentrations (0.1-20.0 mg/L) and no interference with other antiepileptic drugs, benzodiazepines, and tricyclic antidepressants were the other characteristics of the method. The innovation of this method is the use of ISRP column and the choice of detection wavelength, which allow a shorter analysis time (5-6 minutes). The possibility of direct injection of plasma samples into the column permits a reduction in reagent consumption and in analytic steps, and hence in analytic error.
引用
收藏
页码:665 / 668
页数:4
相关论文
共 13 条
[1]   VALIDATION OF A RADIOIMMUNOASSAY FOR THE DETERMINATION OF HUMAN PLASMA-CONCENTRATIONS OF LAMOTRIGINE [J].
BIDDLECOMBE, RA ;
DEAN, KL ;
SMITH, CD ;
JEAL, SC .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1990, 8 (8-12) :691-694
[2]   Lamotrigine drug interactions in a TDM material [J].
Böttiger, Y ;
Svensson, JO ;
Ståhle, L .
THERAPEUTIC DRUG MONITORING, 1999, 21 (02) :171-174
[3]   LAMOTRIGINE [J].
BRODIE, MJ .
LANCET, 1992, 339 (8806) :1397-1400
[4]  
CHEUNG H, 1992, EPILEPSY RES, V13, P107
[5]   LAMOTRIGINE, A NEW ANTICONVULSANT - PHARMACOKINETICS IN NORMAL HUMANS [J].
COHEN, AF ;
LAND, GS ;
BREIMER, DD ;
YUEN, WC ;
WINTON, C ;
PECK, AW .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1987, 42 (05) :535-541
[6]  
DOIG MV, 1991, J CHROMATOGR, V554, P181, DOI 10.1016/S0021-9673(01)88448-X
[7]   A LIQUID-CHROMATOGRAPHIC ASSAY USING A HIGH-SPEED COLUMN FOR THE DETERMINATION OF LAMOTRIGINE, A NEW ANTIEPILEPTIC DRUG, IN HUMAN PLASMA [J].
FAZIO, A ;
ARTESI, C ;
RUSSO, M ;
TRIO, R ;
OTERI, G ;
PISANI, F .
THERAPEUTIC DRUG MONITORING, 1992, 14 (06) :509-512
[8]   PHARMACOLOGICAL STUDIES ON LAMOTRIGINE, A NOVEL POTENTIAL ANTIEPILEPTIC DRUG .2. NEUROCHEMICAL STUDIES ON THE MECHANISM OF ACTION [J].
LEACH, MJ ;
MARDEN, CM ;
MILLER, AA .
EPILEPSIA, 1986, 27 (05) :490-497
[9]  
PECK AW, 1991, EPILEPSIA S, V2, P9
[10]   MEASUREMENT OF LAMOTRIGINE UNDER CONDITIONS MEASURING PHENOBARBITONE, PHENYTOIN, AND CARBAMAZEPINE USING REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY AT DUAL WAVELENGTHS [J].
RAMACHANDRAN, S ;
UNDERHILL, S ;
JONES, SR .
THERAPEUTIC DRUG MONITORING, 1994, 16 (01) :75-82