Literature DB >> 22014024

Colloidal gold modified with a genetically engineered nitroreductase: toward a novel enzyme delivery system for cancer prodrug therapy.

Vanessa V Gwenin1, Chris D Gwenin, Maher Kalaji.   

Abstract

Directed enzyme prodrug therapy is an extensive area of research in cancer chemotherapy. Although very promising, the current directed approaches are still hampered by inefficient enzyme expression and tumor targeting. This work investigates the viability of using metal nanoparticles as a novel delivery vehicle for prodrug-activating enzymes. Using genetically incorporated amino acid sequences, a nitroreductase from E. coli was directly immobilized onto a 50 nm gold colloid, as confirmed by gel electrophoresis, DLS, and UV-vis spectroscopy. The resulting conjugates showed excellent stability in changing proton and sodium chloride environments, including PBS at 37 °C. Remarkably, the immobilized nitroreductase retained more than 99% activity to the CB1954 prodrug without the need for stabilizers. This work provides the foundation for attaching prodrug-activating enzymes to metal nanoparticles for future use in directed enzyme prodrug therapy.
© 2011 American Chemical Society

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 22014024     DOI: 10.1021/la202951p

Source DB:  PubMed          Journal:  Langmuir        ISSN: 0743-7463            Impact factor:   3.882


  8 in total

1.  Magnetic tumor targeting of β-glucosidase immobilized iron oxide nanoparticles.

Authors:  Jie Zhou; Jian Zhang; Allan E David; Victor C Yang
Journal:  Nanotechnology       Date:  2013-08-23       Impact factor: 3.874

2.  Enhanced and selective delivery of enzyme therapy to 9L-glioma tumor via magnetic targeting of PEG-modified, β-glucosidase-conjugated iron oxide nanoparticles.

Authors:  Jie Zhou; Jian Zhang; Wenxi Gao
Journal:  Int J Nanomedicine       Date:  2014-06-10

3.  Oxcarbazepine-loaded polymeric nanoparticles: development and permeability studies across in vitro models of the blood-brain barrier and human placental trophoblast.

Authors:  Antonio Lopalco; Hazem Ali; Nunzio Denora; Erik Rytting
Journal:  Int J Nanomedicine       Date:  2015-03-11

4.  Utilization of Enzyme-Immobilized Mesoporous Silica Nanocontainers (IBN-4) in Prodrug-Activated Cancer Theranostics.

Authors:  Bau-Yen Hung; Yaswanth Kuthati; Ranjith Kumar Kankala; Shravankumar Kankala; Jin-Pei Deng; Chen-Lun Liu; Chia-Hung Lee
Journal:  Nanomaterials (Basel)       Date:  2015-12-04       Impact factor: 5.076

5.  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 6.  Superparamagnetic iron oxide nanoparticles: magnetic nanoplatforms as drug carriers.

Authors:  Sumit Arora
Journal:  Int J Nanomedicine       Date:  2012-07-06

7.  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

8.  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

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.