| Literature DB >> 28150217 |
Autumn D Paro1,2, Ilanchezhian Shanmugam2,3, Anne L van de Ven4,5.
Abstract
Metallic nanoparticles with a high atomic number release Auger electrons in response to external beam X-ray radiation. When these nanoparticles are selectively delivered to tumors, they have the potential to locally enhance the effects of radiation therapy. Optimizing the therapeutic efficacy of these nanoparticles, however, remains a challenging and time-consuming task. Here we describe three different assays that can be used to experimentally quantify and optimize the in vitro therapeutic efficacy of nanoparticle-mediated X-ray radiation enhancement. These include an IC50 extended dose response curve, clonogenic cell survival assay, and immunoblotting. Collectively, these assays provide information about whether a given nanoparticle provides radiosensitization, the extent of the radiosensitization, and the potential mechanism of radiosensitization.Entities:
Keywords: Clonogenic assay; DNA damage; IC50; Immunoblotting; Metallic nanoparticles; Radiosensitization; Surviving fraction
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Year: 2017 PMID: 28150217 PMCID: PMC5512559 DOI: 10.1007/978-1-4939-6646-2_25
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745