Determination of SU5416, a novel angiogenesis inhibitor, in human plasma by liquid chromatography

被引:1
|
作者
Tohnya, TM [1 ]
Kim, S [1 ]
Fine, HA [1 ]
Dunn, L [1 ]
Figg, WD [1 ]
Sparreboom, A [1 ]
机构
[1] NCI, Ctr Canc Res, Clin Pharmacol Res Core, Med Oncol Clin Res Unit, Bethesda, MD 20892 USA
关键词
SU5416; angiogenesis inhibitor;
D O I
10.1016/j.jchromb.2004.02.036
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A high-performance liquid chromatographic (HPLC) assay with UV detection has been developed for the quantitative determination of the antiangiogenic agent SU5416 in human plasma. Sample pretreatment involved a single protein-precipitation step with acetonitrile containing the internal standard. chrysin. Separation of the compounds of interest was achieved on a column packed with HP Zorbax C-8 material (5 mum particle size: length: 150 mm: i.d.: 4.6 mm) using a dual solvent system of 0.01 M aqueous ammonium acetate and acetonitrile delivered as a nonlinear gradient at a flow-rate of 1.00 ml/min. Simultaneous UV detection was performed at 440 nm (SU5416) and 268 nm (chrysin). The calibration graph was fit to log-transformed response-concentration data over a range of 10-5000 ng/ml. Values for accuracy and precision, obtained from six quality controls analyzed on different days in replicates of 3 or 6, ranged 92.9-109 and 0.8-6.2%, respectively. The developed method was successfully applied to study the pharmacokinetics of SU5416 in a cancer patient receiving the drug as a I h infusion. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:135 / 140
页数:6
相关论文
共 50 条
  • [41] Mechanisms underlying the synergistic effect of SU5416 and cisplatin on cytotoxicity in human ovarian tumor cells
    Zhong, XS
    Li, XP
    Wang, GD
    Zhu, YF
    Hu, GD
    Zhao, JS
    Neace, C
    Ding, H
    Reed, E
    Li, QQ
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2004, 25 (02) : 445 - 451
  • [42] SU5416,a novel receptor tyrosine kinase inhibitor, in the treatment of patients with refractory, c-kit positive, acute myeloid leukemia.
    Fiedler, W
    Mesters, R
    Staib, P
    Kuse, R
    Duehrsen, U
    Flasshove, M
    Truemper, L
    Cavalli, F
    Ottmann, O
    Kelsey, S
    Scigalla, P
    Loges, S
    Tinnefeld, H
    Hossfeld, DK
    Berdel, WE
    BLOOD, 2001, 98 (11) : 124A - 124A
  • [43] Expression and localization of vascular endothelial growth factor and its receptors in the pig uterus during peri-implantation and determination of the in vitro effect of the angiogenesis inhibitor SU5416 on VEGF system expression
    Lopez, Rodrigo Gonz
    del Castillo, David Alejandro Contreras Caro
    Magana, Griselda Valdez
    Silva, Rosa Elena Sarmiento
    Castaneda, Francisco Ernesto Martinez
    Ortega, Maria Elena Trujillo
    THERIOGENOLOGY, 2023, 207 : 49 - 60
  • [44] Triple combination of irradiation, chemotherapy (pemetrexed), and VEGFR inhibition (SU5416) in human endothelial and tumor cells
    Bischof, M
    Abdollahi, A
    Gong, P
    Stoffregen, C
    Lipson, KE
    Debus, J
    Weber, KJ
    Huber, PE
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 60 (04): : 1220 - 1232
  • [45] Determination of melagatran, a novel, direct thrombin inhibitor, in human plasma and urine by liquid chromatography-mass spectrometry
    Larsson, M
    Logren, U
    Ahnoff, M
    Lindmark, B
    Abrahamsson, P
    Svennberg, H
    Persson, BA
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2002, 766 (01): : 47 - 55
  • [46] Inflammatory breast cancer as a model disease to study tumor angiogenesis: Results of a phase IB trial of combination SU5416 and doxorubicin
    Overmoyer, Beth
    Fu, Pingfu
    Hoppel, Charles
    Radivoyevitch, Tomas
    Shenk, Robert
    Persons, Marjie
    Silverman, Paula
    Robertson, Kelly
    Ziats, Nicholas P.
    Wasman, Jay K.
    Abdul-Karim, Fadi W.
    Jesberger, John A.
    Duerk, Jeffrey
    Hartman, Paul
    Hanks, Shelli
    Lewin, Jonathan
    Dowlati, Afshin
    McCrae, Keith
    Ivy, Percy
    Remick, Scot C.
    CLINICAL CANCER RESEARCH, 2007, 13 (19) : 5862 - 5868
  • [47] The multi-targeted kinase inhibitor SU5416 inhibits small cell lung cancer growth and angiogenesis, in part by blocking Kit-mediated VEGF expression
    Litz, J
    Warshamana-Greene, GS
    Sulanke, G
    Lipson, KE
    Krystal, GW
    LUNG CANCER, 2004, 46 (03) : 283 - 291
  • [48] Stable remission after administration of the receptor tyrosine kinase inhibitor SU5416 in a patient with refractory acute myeloid leukemia
    Mesters, RM
    Padró, T
    Bieker, R
    Steins, M
    Kreuter, M
    Göner, M
    Kelsey, S
    Scigalla, P
    Fiedler, W
    Büchner, T
    Berdel, WE
    BLOOD, 2001, 98 (01) : 241 - 243
  • [49] Improved effect of an antiangiogenic tyrosine kinase inhibitor (SU5416) by combinations with fractionated radiotherapy or low molecular weight heparin
    Lund, EL
    Olsen, MWB
    Lipson, KE
    McMahon, G
    Howlett, AR
    Kristjansen, PEG
    NEOPLASIA, 2003, 5 (02): : 155 - 160
  • [50] Activity profile of SU5416, a small molecule Flk-1/KDR inhibitor, in tumor xenograft models.
    Cherrington, JM
    Laird, AD
    Strawn, L
    Shenoy, N
    Tang, F
    Blake, R
    Yamada, Y
    Yonekura, K
    McMahon, G
    Shawver, L
    CLINICAL CANCER RESEARCH, 1999, 5 : 3812S - 3812S