| Literature DB >> 30611856 |
Mehri Mirrahimi1, Ziaeddin Abed1, Jaber Beik1, Isaac Shiri2, Amin Shiralizadeh Dezfuli3, Vahid Pirhajati Mahabadi4, S Kamran Kamrava5, Habib Ghaznavi6, Ali Shakeri-Zadeh7.
Abstract
The current interest in cancer research is being shifted from individual therapy to combinatorial therapy. In this contribution, a novel multifunctional nanoplatform comprising alginate nanogel co-loaded with cisplatin and gold nanoparticles (AuNPs) has been firstly developed to combine photothermal therapy and chemotherapy. The antitumor efficacy of the as-prepared nanocomplex was tested against CT26 colorectal tumor model. The nanocomplex showed an improved chemotherapy efficacy than free cisplatin and caused a significantly higher tumor inhibition rate. The in vivo thermometry results indicated that the tumors treated with the nanocomplex had faster temperature rise rate under 532 nm laser irradiation and received dramatically higher thermal doses due to optical absorption properties of AuNPs. The combined action of chemo-photothermal therapy using the nanocomplex dramatically suppressed tumor growth up to 95% of control and markedly prolonged the animal survival rate. Moreover, tumor metabolism was quantified by [18F]FDG (2-deoxy-2-[18F]fluoro-D-glucose)-positron emission tomography (PET) imaging and revealed that the combination of the nanocomplex and laser irradiation have the potential to eradicate microscopic residual tumor to prevent cancer relapse. Therefore, the nanocomplex can afford a potent anticancer efficacy whereby heat and drug can be effectively deliver to the tumor, and at the same time the high dose-associated side effects due to the separate application of chemotherapy and thermal therapy could be potentially reduced.Entities:
Keywords: Alginate; Chemo-photothermal therapy; Cisplatin; Gold nanoparticles; Positron emission tomography
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Year: 2019 PMID: 30611856 DOI: 10.1016/j.phrs.2019.01.005
Source DB: PubMed Journal: Pharmacol Res ISSN: 1043-6618 Impact factor: 7.658