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Starch-Capped AgNPs' as Potential Cytotoxic Agents against Prostate Cancer Cells

Title
Starch-Capped AgNPs' as Potential Cytotoxic Agents against Prostate Cancer Cells
Type
Article in International Scientific Journal
Year
2021
Authors
Morais, M
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Machado, V
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Dias, F
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Palmeira, C
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Martins, G
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Fonseca, M
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Martins, CSM
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Teixeira, AL
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Joao A V Prior
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FFUP
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Rui Medeiros
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ICBAS
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Journal
Title: NanomaterialsImported from Authenticus Search for Journal Publications
Vol. 11
Pages: 1-17
ISSN: 2079-4991
Publisher: MDPI
Other information
Authenticus ID: P-00T-BQP
Abstract (EN): One of the major therapeutic approaches of prostate cancer (PC) is androgen deprivation therapy (ADT), but patients develop resistance within 2-3 years, making the development of new therapeutic approaches of great importance. Silver nanoparticles (AgNPs) synthesized through green approaches have been studied as anticancer agents because of their physical-chemical properties. This study explored the cytotoxic capacity of starch-capped AgNPs, synthesized through green methods, in LNCaP and in PC-3 cells, a hormonal-sensitive and hormone-resistant PC cell line, respectively. These AgNPs were synthesized in a microwave pressurized synthesizer and characterized by ultraviolet-visible (UV-Vis) spectroscopy, transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDX). Their cytotoxicity was assessed regarding their ability to alter morphological aspect (optical microscopy), induce damage in cytoplasmic membrane (Trypan Blue Assay), mitochondria (WST-1 assay), cellular proliferation (BrdU assay), and cell cycle (Propidium iodide and flow-cytometry). AgNPs showed surface plasmon resonance (SPR) of approximately 408 nm and average size of 3 nm. The starch-capped AgNPs successfully induced damage in cytoplasmic membrane and mitochondria, at concentrations equal and above 20 ppm. These damages lead to cell cycle arrest in G0/G1 and G2/M, blockage of proliferation and death in LNCaP and PC-3 cells, respectively. This data shows these AgNPs' potential as anticancer agents for the different stages of PC.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 17
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