Bioanalytical method development and validation for a large peptide HIV fusion inhibitor (Enfuvirtide, T-20) and its metabolite in human plasma using LC-MS/MS

被引:48
作者
Chang, D
Kolis, SJ
Linderholm, KH
Julian, TF
Nachi, R
Dzerk, AM
Lin, PP
Lee, JW
Bansal, SK
机构
[1] Hoffmann La Roche Inc, Nutley, NJ 07110 USA
[2] MDS Pharma Serv, Lincoln, NE 68501 USA
关键词
HIV fusion inhibitor; Enfuvirtide; T-20; LC-MS/MS; polypeptide bioanalysis; gp41;
D O I
10.1016/j.jpba.2005.01.024
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method for measuring a human immunodeficiency virus (HIV) cell membrane fusion inhibitor (T-20/Ro 29-9800) and its metabolite (M-20/Ro 50-6343) in human plasma by liquid chromatography tandem mass spectrometry (LC-MS/MS) was developed. The relatively large peptide analytes and their corresponding deuterated (d(10)) peptides used as internal standard were isolated from plasma by protein precipitation with two volumes of acetonitrile to plasma. A large pore size reversed-phase C-18 column was employed to elute the peptides. A triple quadrupole mass spectrometer with electrospray interface operating in positive ion and multiple reaction monitoring modes with transitions m/z 1124 -> 1343 for both T-20 and M-20 was utilized for peak detection. The advantages of the method were a simple sample preparation, specific and sensitive MS/MS detection, and a wide dynamic range of 10-2000 ng/ml for T-20. The method was validated and used for analyzing samples from clinical studies to provide pharmacokinetic profiles of the HIV fusion inhibitor peptide drug and its metabolite. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:487 / 496
页数:10
相关论文
共 12 条
[1]   ENHANCED SENSITIVITY FOR PEPTIDE-MAPPING WITH ELECTROSPRAY LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY IN THE PRESENCE OF SIGNAL SUPPRESSION DUE TO TRIFLUOROACETIC ACID-CONTAINING MOBILE PHASES [J].
APFFEL, A ;
FISCHER, S ;
GOLDBERG, G ;
GOODLEY, PC ;
KUHLMANN, FE .
JOURNAL OF CHROMATOGRAPHY A, 1995, 712 (01) :177-190
[2]  
Bonfiglio R, 1999, RAPID COMMUN MASS SP, V13, P1175, DOI 10.1002/(SICI)1097-0231(19990630)13:12<1175::AID-RCM639>3.3.CO
[3]  
2-S
[4]   Quantitative electrospray LC-MS and LC-MS/MS in biomedicine [J].
Carrascal, M ;
Schneider, K ;
Calaf, RE ;
van Leeuwen, S ;
Canosa, D ;
Gelpí, E ;
Abian, J .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1998, 17 (6-7) :1129-1138
[5]   HIGH-SPEED LIQUID-CHROMATOGRAPHY TANDEM MASS-SPECTROMETRY FOR THE DETERMINATION OF DRUGS IN BIOLOGICAL SAMPLES [J].
COVEY, TR ;
LEE, ED ;
HENION, JD .
ANALYTICAL CHEMISTRY, 1986, 58 (12) :2453-2460
[6]   A mass spectrometric method for quantitation of intact insulin in blood samples [J].
Darby, SM ;
Miller, ML ;
Allen, RO ;
LeBeau, M .
JOURNAL OF ANALYTICAL TOXICOLOGY, 2001, 25 (01) :8-14
[7]  
FDA, 2001, GUID IND BIO METH VA
[8]   Potent suppression of HIV-1 replication in humans by T-20, a peptide inhibitor of gp41-mediated virus entry [J].
Kilby, JM ;
Hopkins, S ;
Venetta, TM ;
DiMassimo, B ;
Cloud, GA ;
Lee, JY ;
Alldredge, L ;
Hunter, E ;
Lambert, D ;
Bolognesi, D ;
Mathews, T ;
Johnson, MR ;
Nowak, MA ;
Shaw, GM ;
Saag, MS .
NATURE MEDICINE, 1998, 4 (11) :1302-1307
[9]   Bioanalytical Method Validation—A Revisit with a Decade of Progress [J].
Vinod P. Shah ;
Kamal K. Midha ;
John W. A. Findlay ;
Howard M. Hill ;
James D. Hulse ;
Iain J. McGilveray ;
Gordon McKay ;
Krys J. Miller ;
Rabindra N. Patnaik ;
Mark L. Powell ;
Alfred Tonelli ;
C. T. Viswanathan ;
Avraham Yacobi .
Pharmaceutical Research, 2000, 17 (12) :1551-1557
[10]   A SYNTHETIC PEPTIDE FROM HIV-1 GP41 IS A POTENT INHIBITOR OF VIRUS-MEDIATED CELL-CELL FUSION [J].
WILD, C ;
GREENWELL, T ;
MATTHEWS, T .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1993, 9 (11) :1051-1053