Literature DB >> 6785339

An enzymatic method for microdetermination of aphidicolin: a promising anticancer drug.

G Pedrali-Noy, C C Kuenzle, F Focher, M Belvedere, S Spadari.   

Abstract

We have developed a method, based on the in vitro inhibition of purified human DNA polymerase alpha, the major enzyme of DNA replication, which allows the rapid and accurate determination of pmol amounts of aphidicolin, a promising anticancer drug. The efficacy of this simple method was verified by the determination of aphidicolin in the liver, spleen, blood and urine of mice treated parenterically with the drug. Given its sensitivity and the avoidance of radioactive tracers, this enzymatic method is suitable for the determination of the drug in body fluids and tissue biopsies from living humans. It allows the detection and quantitation of aphidicolin in the presence of inactive metabolite(s) with very similar chemical structure(s) such as those generated by liver microsomal oxidases. The technique will also be useful to monitor the purification of the drug from cultures of Cephalosporium aphidicola.

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Year:  1981        PMID: 6785339     DOI: 10.1016/0165-022x(81)90024-5

Source DB:  PubMed          Journal:  J Biochem Biophys Methods        ISSN: 0165-022X


  3 in total

1.  Common fragile sites are conserved features of human and mouse chromosomes and relate to large active genes.

Authors:  Anne Helmrich; Karen Stout-Weider; Klaus Hermann; Evelin Schrock; Thomas Heiden
Journal:  Genome Res       Date:  2006-09-05       Impact factor: 9.043

2.  Inactivation of aphidicolin by plant cells.

Authors:  F Sala; C Sala; M G Galli; E Nielsen; G Pedrali-Noy; S Spadari
Journal:  Plant Cell Rep       Date:  1983-10       Impact factor: 4.570

3.  Structure-activity relationships for the inhibition of DNA polymerase alpha by aphidicolin derivatives.

Authors:  G Prasad; R A Edelson; P D Gorycki; T L Macdonald
Journal:  Nucleic Acids Res       Date:  1989-08-11       Impact factor: 16.971

  3 in total

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