Literature DB >> 29704231

Management of extravasation of oxaliplatin by mimicking its biotransformation.

F Bahadori1, M Demiray2,3.   

Abstract

Although oxaliplatin (Oxali) plays a key role in the treatment of many types of cancer and has been reported to be an irritant, there is no specific and effective method for its extravasation and failure in Oxali extravasation management results in the need for plastic surgery. In the body, Oxali bio-transforms upon dilution in chloride-containing buffer salts to its di-chloro derivative and loses an oxalate molecule. Consequently, the chloride ions exchange with water molecules in the intracellular environment to produce the di-aqua derivative, which is the most active biotransformation product of Oxali in terms of forming the DNA adducts. Thus, inhibiting transformation of di-chloro to di-aqua derivatives by accumulating chloride ions at the site of extravasation and saturating the Oxali molecule with these ions is a strategy that could help manage extravasation. Injecting normal saline at this site is a simple yet effective way to achieve this goal.

Entities:  

Keywords:  Biotransformation; Chemotherapy; DNA damage; Extravasation; Guideline; Normal saline; Oxaliplatin; Toxicity

Mesh:

Substances:

Year:  2018        PMID: 29704231     DOI: 10.1007/s12094-018-1854-z

Source DB:  PubMed          Journal:  Clin Transl Oncol        ISSN: 1699-048X            Impact factor:   3.405


  13 in total

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4.  Cross-linking of complementary strands of DNA in mammalian cells by antitumour platinum compounds.

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5.  Role of calcium/ magnesium infusion in oxaliplatin-based chemotherapy for colorectal cancer patients.

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6.  Cytotoxicity, cellular uptake, and cellular biotransformations of oxaliplatin in human colon carcinoma cells.

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8.  Comparison of the reactivity of oxaliplatin, pt(diaminocyclohexane)Cl2 and pt(diaminocyclohexane1)(OH2)2(2+) with guanosine and L-methionine.

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Authors:  P Allain; O Heudi; A Cailleux; A Le Bouil; F Larra; M Boisdron-Celle; E Gamelin
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10.  Predicting effects on oxaliplatin clearance: in vitro, kinetic and clinical studies of calcium- and magnesium-mediated oxaliplatin degradation.

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