Quantitative determination of capsaicin, a transient receptor potential channel vanilloid 1 agonist, by liquid chromatography quadrupole ion trap mass spectrometry: evaluation of in vitro metabolic stability

被引:22
作者
Beaudry, Francis [1 ]
Vachon, Pascal [1 ]
机构
[1] Univ Montreal, Fac Vet Med, Dept Vet Biomed, Mass Spectrometry & Med Chem Lab,Grp Rech Pharmac, St Hyacinthe, PQ J2S 2M2, Canada
关键词
capsaicin; bioanalysis; intrinsic clearance; microsomes; metabolism; liquid chromatography; electrospray; mass spectrometry; TRPV1; PHARMACOKINETICS; PREDICTION; EUGENOL;
D O I
10.1002/bmc.1107
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Capsaicin is the most abundant pungent molecule present in red peppers and it is widely used for food flavoring, in pepper spray in self-defense devices and more recently in ointments for the relief of neuropathic pain. Capsaicin is a selective agonist of transient receptor potential channel, vanilloid subfamily member 1. A selective and sensitive quantitative method for the determination of capsaicin by LC-ESI/MS/MS was developed. The method consisted of a protein precipitation extraction followed by analysis using liquid chromatography electrospray quadrupole ion trap mass spectrometry. The chromatographic separation was achieved using a 100 x 2 mm C-18 Waters Symmetry column combined with a gradient mobile phase composed of acetonitrile and 0.1 % formic acid aqueous solution at a flow rate of 220 mu L/min. The mass spectrometer was operating in full-scan MS/MS mode using two-segment analysis. An analytical range of 10-5000 ng/mL was used in the calibration curve constructed in rat plasma. The interbatch precision and accuracy observed were 6.5,6.7,5.3 and 101.2,102.7,103.5% at 50, 500 and 5000 ng/mL, respectively. An in vitro metabolic stability study was performed in rat, dog and mouse liver microsomes and the novel analytical method was adapted and used to determine intrinsic clearance of capsaicin. Results suggest very rapid degradation with T-1/2 ranging from 2.3 to 4.1 min and high clearance values suggesting that drug bioavailability will be considerably reduced, consequently affecting drug response and efficacy. Copyright (c) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:204 / 211
页数:8
相关论文
共 31 条
[1]   Electrospray ionization suppression, a physical or a chemical phenomenon? [J].
Beaudry, F ;
Vachon, P .
BIOMEDICAL CHROMATOGRAPHY, 2006, 20 (02) :200-205
[2]  
Beaudry F., 1999, Pharm Sci, V1, P2437
[3]   Impaired nociception and pain sensation in mice lacking the capsaicin receptor [J].
Caterina, MJ ;
Leffler, A ;
Malmberg, AB ;
Martin, WJ ;
Trafton, J ;
Petersen-Zeitz, KR ;
Koltzenburg, M ;
Basbaum, AI ;
Julius, D .
SCIENCE, 2000, 288 (5464) :306-313
[4]   The capsaicin receptor: a heat-activated ion channel in the pain pathway [J].
Caterina, MJ ;
Schumacher, MA ;
Tominaga, M ;
Rosen, TA ;
Levine, JD ;
Julius, D .
NATURE, 1997, 389 (6653) :816-824
[5]  
*CDER CVM, 2001, GUID IND BIOAN METH
[6]   In vitro hepatic and skin metabolism of capsaicin [J].
Chanda, Sanjay ;
Bashir, Mohammad ;
Babbar, Sunita ;
Koganti, Aruna ;
Bley, Keith .
DRUG METABOLISM AND DISPOSITION, 2008, 36 (04) :670-675
[7]   Biochemical pharmacology of the vanilloid receptor TRPV1 - An update [J].
Cortright, DN ;
Szallasi, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2004, 271 (10) :1814-1819
[8]   Vanilloid receptor-1 is essential for inflammatory thermal hyperalgesia [J].
Davis, JB ;
Gray, J ;
Gunthorpe, MJ ;
Hatcher, JP ;
Davey, PT ;
Overend, P ;
Harries, MH ;
Latcham, J ;
Clapham, C ;
Atkinson, K ;
Hughes, SA ;
Rance, K ;
Grau, E ;
Harper, AJ ;
Pugh, PL ;
Rogers, DC ;
Bingham, S ;
Randall, A ;
Sheardown, SA .
NATURE, 2000, 405 (6783) :183-187
[9]   Determination of capsaicin and dihydrocapsaicin in Capsicum fruits by liquid chromatography-electrospray/time-of-flight mass spectrometry [J].
Garces-Claver, Ana ;
Arnedo-Andres, Maria S. ;
Abadia, Javier ;
Gil-Ortega, Ramiro ;
Alvarez-Fernandez, Ana .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2006, 54 (25) :9303-9311
[10]   Pharmacokinetics and anesthetic activity of eugenol in male Sprague-Dawley rats [J].
Guenette, S. A. ;
Beaudry, F. ;
Marier, J. F. ;
Vachon, P. .
JOURNAL OF VETERINARY PHARMACOLOGY AND THERAPEUTICS, 2006, 29 (04) :265-270