High-performance liquid chromatographic analysis of the anti-tumor agent SCH 66336 in cynomolgus monkey plasma and evaluation of its chiral inversion in animals

被引:9
作者
Kim, H
Likhari, P
Lin, CC
Nomeir, AA
机构
[1] Schering Plough Res Inst, Dept Drug Metab & Pharmacokinet, Kenilworth, NJ 07033 USA
[2] Bioassay Lab, Houston, TX 77099 USA
来源
JOURNAL OF CHROMATOGRAPHY B | 1999年 / 728卷 / 01期
关键词
SCH; 66336;
D O I
10.1016/S0378-4347(99)00070-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
SCH 66336 is a novel non-cytotoxic anti-tumor agent that is in phase I/II clinical trials for the treatment of solid tumors. This compound is a single enantiomer with one chiral center. Prior to evaluation of this drug candidate in man, it was necessary to evaluate its pharmacokinetics and possible chiral inversion in animals. Thus, high-performance liquid chromatographic (HPLC) methods have been developed for its determination in cynomolgus monkey plasma and for the evaluation of its chiral inversion in rats and cynomolgus monkeys. The achiral HPLC analysis involved extraction with 30% methylene chloride in hexane followed by separation on a CN column and quantitation by UV absorbance at 280 nm. The method was linear over a concentration range of 0.1 to 20 mu g/ml in monkey plasma. The chiral HPLC analysis involved the use of a Chiralpak AD column set at 39 degrees C with a mobile phase of hexime-ethanol-diethylamine mixture and a UV detector set at 280 nm. Plasma samples were subjected to solid-phase extraction on a C-2 cartridge prior to HPLC analysis. The method was linear over a concentration range of 0.25 to 10 mu g/ml in rat and cynomolgus monkey plasma for both enantiomers. Both methods showed good linearity (r(2)>0.99), accuracy (bias<13%) and precision (CV<12%). Chiral HPLC analysis indicated that SCH 66336 was not subjected to chiral inversion in rats and cynomolgus monkeys (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:133 / 141
页数:9
相关论文
共 16 条
  • [1] RAS GENES
    BARBACID, M
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 : 779 - 827
  • [2] Novel tricyclic inhibitors of farnesyl protein transferase - Biochemical characterization and inhibition of Ras modification in transfected Cos cells
    Bishop, WR
    Bond, R
    Petrin, J
    Wang, L
    Patton, R
    Doll, R
    Njoroge, G
    Catino, J
    Schwartz, J
    Windsor, W
    Syto, R
    Schwartz, J
    Carr, D
    James, L
    Kirschmeier, P
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (51) : 30611 - 30618
  • [3] P21RAS IS MODIFIED BY A FARNESYL ISOPRENOID
    CASEY, PJ
    SOLSKI, PA
    DER, CJ
    BUSS, JE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (21) : 8323 - 8327
  • [4] GARCIA AM, 1993, J BIOL CHEM, V268, P18415
  • [5] GILBALDI M, 1982, PHARMACOKINETICS, P409
  • [6] GLOMSET JA, 1994, ANNU REV CELL BIOL, V10, P181, DOI 10.1146/annurev.cb.10.110194.001145
  • [7] SEPARATION OF DRUG ENANTIOMERS BY HPLC USING CHIRAL STATIONARY PHASES - A SELECTIVE REVIEW
    GUBITZ, G
    [J]. CHROMATOGRAPHIA, 1990, 30 (9-10) : 555 - 564
  • [8] ALL RAS PROTEINS ARE POLYISOPRENYLATED BUT ONLY SOME ARE PALMITOYLATED
    HANCOCK, JF
    MAGEE, AI
    CHILDS, JE
    MARSHALL, CJ
    [J]. CELL, 1989, 57 (07) : 1167 - 1177
  • [9] ENANTIOSELECTIVE ASPECTS OF DRUG-ACTION AND DISPOSITION - THERAPEUTIC PITFALLS
    JAMALI, F
    MEHVAR, R
    PASUTTO, FM
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 1989, 78 (09) : 695 - 715
  • [10] BENZODIAZEPINE PEPTIDOMIMETICS - POTENT INHIBITORS OF RAS FARNESYLATION IN ANIMAL-CELLS
    JAMES, GL
    GOLDSTEIN, JL
    BROWN, MS
    RAWSON, TE
    SOMERS, TC
    MCDOWELL, RS
    CROWLEY, CW
    LUCAS, BK
    LEVINSON, AD
    MARSTERS, JC
    [J]. SCIENCE, 1993, 260 (5116) : 1937 - 1942