Literature DB >> 30414836

Time dependent HPLC analysis of the product ratio of enzymatically reduced prodrug CB1954 by a modified and immobilised nitroreductase.

Patrick Ball1, Emma Thompson1, Simon Anderson1, Vanessa Gwenin1, Chris Gwenin2.   

Abstract

Directed enzyme prodrug therapy is a chemotherapy strategy that utilises prodrug-activating enzymes to activate prodrugs at the tumour location, thus reducing off-target effects. The most commonly investigated enzyme for use with the CB1954 prodrug is the NfnB nitroreductase from E. coli. Literature states that CB1954 is reduced by NfnB at the 2- or 4-position at a 1:1 ratio; deviation from this ratio has been observed in the literature, but not further investigated. The kinetic parameters for the genetically-modified enzymes; NfnB-his, NfnB-cys and AuNP-NfnB-cys were assessed and HPLC analysis was used to determine the hydroxylamine product ratios formed when reacted with CB1954. Time-dependent HPLC studies were carried out to assess how this ratio changes over time. It was shown that the hydroxylamine ratio formed by the reduction of CB1954 by a nitroreductase changes over time and that this change in ratio relates directly to the kinetics of the reaction. Thus, the hydroxylamine ratio measured using HPLC at a given time point was not a true indication of the preference of the nitroreductase enzymes during catalysis. These results question how nitroreductases are evaluated in terms of the hydroxylamine ratio and it is suspected that this phenomenon may also apply to other enzyme/prodrug combinations. Crown
Copyright © 2018. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  CB1954; DEPT; HPLC; Nitroreductase; Prodrug

Mesh:

Substances:

Year:  2018        PMID: 30414836     DOI: 10.1016/j.ejps.2018.11.001

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  4 in total

1.  The YfkO Nitroreductase from Bacillus Licheniformis on Gold-Coated Superparamagnetic Nanoparticles: Towards a Novel Directed Enzyme Prodrug Therapy Approach.

Authors:  Patrick Ball; Robert Hobbs; Simon Anderson; Emma Thompson; Vanessa Gwenin; Christopher Von Ruhland; Christopher Gwenin
Journal:  Pharmaceutics       Date:  2021-04-09       Impact factor: 6.321

Review 2.  The Role of Nitroreductases in Resistance to Nitroimidazoles.

Authors:  Carol Thomas; Christopher D Gwenin
Journal:  Biology (Basel)       Date:  2021-05-01

3.  Cell-Penetrating Peptides as a Tool for the Cellular Uptake of a Genetically Modified Nitroreductase for use in Directed Enzyme Prodrug Therapy.

Authors:  Simon D Anderson; Robert J Hobbs; Vanessa V Gwenin; Patrick Ball; Lindsey A Bennie; Jonathan A Coulter; Chris D Gwenin
Journal:  J Funct Biomater       Date:  2019-10-01

4.  Evaluation of two xenobiotic reductases from Pseudomonas putida for their suitability for magnetic nanoparticle-directed enzyme prodrug therapy as a novel approach to cancer treatment.

Authors:  Patrick Ball; Jennifer Halliwell; Simon Anderson; Vanessa Gwenin; Christopher Gwenin
Journal:  Microbiologyopen       Date:  2020-09-26       Impact factor: 3.139

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.