Ormaplatin [tetrachloro(d,1-trans) 1,2-diaminocyclohexaneplatinum(IV)] (also known as tetraplatin) is a second generation platinum drug that has recently entered phase I clinical trials. We have characterized the biotransformation of ormaplatin in tissue culture medium, in L1210 cells, and in rat plasma (both in vitro and in vivo). We have also shown that both diethyldithiocarbonate (DDTC) and S-2(3-aminopropylamino)ethylphosphorothioic acid (WR-2721) are effective at reducing ormaplatin toxicity in the Fischer-344 rat and have characterized the effects of DDTC on the plasma biotransformations or ormaplatin. We now propose the following: (1) We plan to determine the and therapeutic effectiveness of the major plasma biotransformation products. These data should allow one to optimize the therapeutic potential of ormaplatin by selecting protocols that maximize the therapeutically effective biotransformation products and minimize the toxic ones. (2) We plan to characterize the intracellular biotransformations of ormaplatin in various tissues (liver, kidney, spleen and intestine) of the rat. These studies should allow a better understanding of the tissue selective toxicity of ormaplatin and other platinum drugs. (3) We plan to determine the effects of DDTC and WR-2721 on the intracellular tissue biotransformations of ormaplatin. In the case of DDTC we also plan to quantitate its effectiveness at removing Pt-protein adducts and quenching PtDNA monoadducts in the same tissues. (4) We also plan to determine the effect of i.v. sodium thiosulfate on the toxicity of i.p. ormaplatin in the Fischer-344 rat and determine the effect of thiosulfate on the peritoneal, plasma and tissue biotranformations of ormaplatin under the same treatment conditions. These studies should improve our understanding of how these compounds reduce the toxicity of ormaplatin and related compounds such as cisplatin. These data might also allow the selection and/or design of modifiers which have improved selectivity for reducing the toxic side effects of platinum drugs without intefering with their therapeutic usefulness.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA055326-02
Application #
3199849
Study Section
Experimental Therapeutics Subcommittee 1 (ET)
Project Start
1991-07-01
Project End
1994-06-30
Budget Start
1992-07-01
Budget End
1993-06-30
Support Year
2
Fiscal Year
1992
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Medicine
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
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Luo, F R; Wyrick, S D; Chaney, S G (1999) Biotransformations of oxaliplatin in rat blood in vitro. J Biochem Mol Toxicol 13:159-69
Luo, F R; Wyrick, S D; Chaney, S G (1999) Comparative neurotoxicity of oxaliplatin, ormaplatin, and their biotransformation products utilizing a rat dorsal root ganglia in vitro explant culture model. Cancer Chemother Pharmacol 44:29-38
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Holmes, J; Stanko, J; Varchenko, M et al. (1998) Comparative neurotoxicity of oxaliplatin, cisplatin, and ormaplatin in a Wistar rat model. Toxicol Sci 46:342-51
Chaney, S G; Sancar, A (1996) DNA repair: enzymatic mechanisms and relevance to drug response. J Natl Cancer Inst 88:1346-60
Sakata, M; Chaney, S G; Spriggs, D R (1995) Possible correlation between ormaplatin biotransformations and neurotoxicity. Oncol Res 7:67-71
Thompson, D C; Vaisman, A; Sakata, M K et al. (1995) Organ-specific biotransformation of ormaplatin in the Fischer 344 rat. Cancer Chemother Pharmacol 36:439-47
Thompson, D C; Wyrick, S D; Holbrook, D J et al. (1995) Effects of anesthetics on ormaplatin biotransformations in the Fischer 344 rat. Cancer Invest 13:555-7

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