Electrospray ionization mass spectrometry coupled to reversed-phase ion-pair high-performance liquid chromatography for quantitation of sodium borocaptate and application to pharmacokinetic analysis

被引:10
作者
Gibson, CR
Staubus, AE
Barth, RF
Yang, WL
Kleinholz, NM
Jones, RB
Green-Church, KB
Tjarks, W
Soloway, AH
机构
[1] Ohio State Univ, Coll Pharm, Dept Pathol, Columbus, OH 43210 USA
[2] Ohio State Univ, Campus Chem Instrumentat Ctr, Mass Spectrometry Facil, Columbus, OH 43210 USA
关键词
D O I
10.1021/ac0112723
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have developed a quantitative assay using electrospray ionization mass spectrometry coupled to reversed-phase ion-pair liquid chromatography (LC/MS) for quantitation of sodium borocaptate (BSH) in human plasma. The assay was developed using a Micromass Q-TOF II mass spectrometer equipped with an orthogonal electrospray source. The mobile phase was a 1:1 solution of methanol and 5 mM aqueous tetrabutylammonium acetate flowing at 0.2 mL/min, and the chromatography was performed using a Machery-Nagel Nucleosil C18 column. Plasma samples from patients who had received an intravenous infusion of sodium borocaptate (Na2B12H11SH), frequently referred to as BSH, were prepared for analysis by precipitation with acetonitrile. Following this, the supernatants were collected, and 40 muL was injected onto the column for analysis. The LC/MS assay was linear over a BSH plasma concentration range of 20-0.5 mug/mL with acceptable variability for both intra- and interassay precision. The LC/MS assay was used to generate pilot pharmacokinetic data for the plasma disposition of BSH in humans. The disposition of BSH was found to be consistent with a two-compartment model with first-order elimination from the central compartment. The mean total body plasma clearance was 95.7 +/- 30.8 mL/min and the harmonic mean terminal half-life was 3.6 h.
引用
收藏
页码:2394 / 2399
页数:6
相关论文
共 20 条
[1]   Identification of adenine nucleotide-containing metabolites of bisphosphonate drugs using ion-pair liquid chromatography-electrospray mass spectrometry [J].
Auriola, S ;
Frith, J ;
Rogers, MJ ;
Koivuniemi, A ;
Mönkkönen, J .
JOURNAL OF CHROMATOGRAPHY B, 1997, 704 (1-2) :187-195
[2]   DETERMINATION OF BORON IN TISSUES AND CELLS USING DIRECT-CURRENT PLASMA ATOMIC EMISSION-SPECTROSCOPY [J].
BARTH, RF ;
ADAMS, DM ;
SOLOWAY, AH ;
MECHETNER, EB ;
ALAM, F ;
ANISUZZAMAN, AKM .
ANALYTICAL CHEMISTRY, 1991, 63 (09) :890-893
[3]   Boron neutron capture therapy of brain tumors: An emerging therapeutic modality [J].
Barth, RF ;
Soloway, AH ;
Goodman, JH ;
Gahbauer, RA ;
Gupta, N ;
Blue, TE ;
Yang, WL ;
Tjarks, W .
NEUROSURGERY, 1999, 44 (03) :433-450
[4]   STATISTICAL ESTIMATIONS IN PHARMACOKINETICS [J].
BOXENBAU.HG ;
RIEGELMA.S ;
ELASHOFF, RM .
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1974, 2 (02) :123-148
[5]   The radiation biology of boron neutron capture therapy [J].
Coderre, JA ;
Morris, GM .
RADIATION RESEARCH, 1999, 151 (01) :1-18
[6]   Pharmacokinetics of Na2B12H11SH (BSH) in patients with malignant brain tumours as prerequisite for a phase I clinical trial of boron neutron capture [J].
Gabel, D ;
Preusse, D ;
Haritz, D ;
Grochulla, F ;
Haselsberger, K ;
Fankhauser, H ;
Ceberg, C ;
Peters, HD ;
Klotz, U .
ACTA NEUROCHIRURGICA, 1997, 139 (07) :606-612
[7]  
Gibson CR, 2001, DRUG METAB DISPOS, V29, P1588
[8]  
Goodman JH, 2000, NEUROSURGERY, V47, P608
[9]   CLINICAL PHASE-I STUDY OF NA2B12H11SH (BSH) IN PATIENTS WITH MALIGNANT GLIOMA AS PRECONDITION FOR BORON NEUTRON-CAPTURE THERAPY (BNCT) [J].
HARITZ, D ;
GABEL, D ;
HUISKAMP, R .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1994, 28 (05) :1175-1181
[10]  
HASELSBERGER K, 1994, CANCER RES, V54, P6318