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Blue-LED assisted Photodegradation kinetics of rhodamine-6G dye, enhanced anticancer activity and cleavage of plasmids using Au-ZnO nanocomposite

The plasmonic metal doping on the UV-active metal oxide nanoparticle turns the resultant plasmonic metal-metal oxide (PMMO) into visible light active and upon exogenous illumination the photogenerated energetic charge carriers and the in situ generated reactive oxygen species (ROS, e.g. ·OH and O2−·...

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Published in:Heliyon 2025-01, Vol.11 (1), p.e41061, Article e41061
Main Authors: Thangamuniyandi, Pilavadi, Umapathy, Devan, Nagarajan, Loganathan, Velanganni Arockiam, Antony Joseph
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description The plasmonic metal doping on the UV-active metal oxide nanoparticle turns the resultant plasmonic metal-metal oxide (PMMO) into visible light active and upon exogenous illumination the photogenerated energetic charge carriers and the in situ generated reactive oxygen species (ROS, e.g. ·OH and O2−·) authoritatively enhances its biological and catalytic activity. Herein, a hexagonal rod-shaped ZnO nanoparticles (NP) precursor was prepared using the sol-gel method, which in the presence of varying concentrations of gold (0.005M, 0.01M, and 0.015M) via a greener citrate reduction method afforded a nanocrystalline Au-ZnO nanocomposite. Using which, the visible-light driven photo-degradation kinetics investigation of rhodamine-6G (R6G) dye under blue LED irradiation were carried out. The use of 20 mg 0.015-Au-ZnO completes the degradation of R6G (97.0 %, k = 6.5 X 10−3s−1 at pH 7) within 55 min while 50 mg of 0.015-Au-ZnO catalyst improves the rate of R6G degradation (15 min 97.8 %, k = 14.8 × 10−3 s−1) and it is reusable up to three cycles. The LC-MS spectra of the remains of R6G (after 15 min) identified various low molecular ions (up m/z = 65). Further, the blue-LED assisted anti-cancer studies (MTT assay) using 0.015-Au-ZnO towards human lung cancer cells (A549), breast cancer cells (SKBr3) show high anti-proliferation rate and low cytotoxicity against healthy human embryonic kidney cells (HEK-293) with an IC50 value of 65, 53 and 124 μg/mL respectively. Also, the AO-EB dual staining and DCFH-DA analysis of SKBr3 and A549 cells revealed ROS-mediated cell death via apoptosis. Moreover, plasmid cleavage studies against supercoiled pBR322 DNA result in single-stranded linear DNA without traversing the nicked circular form, suggesting the possible DNA targeting activity of Au-ZnO nanozyme. Thus, the synthesized Au-ZnO nanocomposite shows excellent photocatalytic and biological activity. [Display omitted] •A greener citrate reduction method was employed to synthesize plasmonic metal-metal oxide (PMMO) such as Au-ZnO nanocomposites with various concentrations of gold.•Au-ZnO was utilized to perform a blue LED driven Rhodamine-6G dye degradation and 0.015-Au-ZnO is exceedingly good ((98 %, 15 min, 0.014 s−1).•Au-ZnO shows excellent anti-cancer activity against both SKBR3 and A549 cells owing to the in-situ generation of reactive oxygen species (ROS) under blue LED illumination.•EPR studies with TEMPO after LED exposure trap the in situ generated ROS species such
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Herein, a hexagonal rod-shaped ZnO nanoparticles (NP) precursor was prepared using the sol-gel method, which in the presence of varying concentrations of gold (0.005M, 0.01M, and 0.015M) via a greener citrate reduction method afforded a nanocrystalline Au-ZnO nanocomposite. Using which, the visible-light driven photo-degradation kinetics investigation of rhodamine-6G (R6G) dye under blue LED irradiation were carried out. The use of 20 mg 0.015-Au-ZnO completes the degradation of R6G (97.0 %, k = 6.5 X 10−3s−1 at pH 7) within 55 min while 50 mg of 0.015-Au-ZnO catalyst improves the rate of R6G degradation (15 min 97.8 %, k = 14.8 × 10−3 s−1) and it is reusable up to three cycles. The LC-MS spectra of the remains of R6G (after 15 min) identified various low molecular ions (up m/z = 65). Further, the blue-LED assisted anti-cancer studies (MTT assay) using 0.015-Au-ZnO towards human lung cancer cells (A549), breast cancer cells (SKBr3) show high anti-proliferation rate and low cytotoxicity against healthy human embryonic kidney cells (HEK-293) with an IC50 value of 65, 53 and 124 μg/mL respectively. Also, the AO-EB dual staining and DCFH-DA analysis of SKBr3 and A549 cells revealed ROS-mediated cell death via apoptosis. Moreover, plasmid cleavage studies against supercoiled pBR322 DNA result in single-stranded linear DNA without traversing the nicked circular form, suggesting the possible DNA targeting activity of Au-ZnO nanozyme. Thus, the synthesized Au-ZnO nanocomposite shows excellent photocatalytic and biological activity. [Display omitted] •A greener citrate reduction method was employed to synthesize plasmonic metal-metal oxide (PMMO) such as Au-ZnO nanocomposites with various concentrations of gold.•Au-ZnO was utilized to perform a blue LED driven Rhodamine-6G dye degradation and 0.015-Au-ZnO is exceedingly good ((98 %, 15 min, 0.014 s−1).•Au-ZnO shows excellent anti-cancer activity against both SKBR3 and A549 cells owing to the in-situ generation of reactive oxygen species (ROS) under blue LED illumination.•EPR studies with TEMPO after LED exposure trap the in situ generated ROS species such as O2−. radical.</description><identifier>ISSN: 2405-8440</identifier><identifier>EISSN: 2405-8440</identifier><identifier>DOI: 10.1016/j.heliyon.2024.e41061</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Acridine orange-ethidium bromide (AO-EB) dual staining ; Apoptosis ; Plasmide cleavage ; Plasmonic metal-metal oxide ; Rhodamine-6G Photodegradation</subject><ispartof>Heliyon, 2025-01, Vol.11 (1), p.e41061, Article e41061</ispartof><rights>2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0003-2879-3092</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2405844024170922$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids></links><search><creatorcontrib>Thangamuniyandi, Pilavadi</creatorcontrib><creatorcontrib>Umapathy, Devan</creatorcontrib><creatorcontrib>Nagarajan, Loganathan</creatorcontrib><creatorcontrib>Velanganni Arockiam, Antony Joseph</creatorcontrib><title>Blue-LED assisted Photodegradation kinetics of rhodamine-6G dye, enhanced anticancer activity and cleavage of plasmids using Au-ZnO nanocomposite</title><title>Heliyon</title><description>The plasmonic metal doping on the UV-active metal oxide nanoparticle turns the resultant plasmonic metal-metal oxide (PMMO) into visible light active and upon exogenous illumination the photogenerated energetic charge carriers and the in situ generated reactive oxygen species (ROS, e.g. ·OH and O2−·) authoritatively enhances its biological and catalytic activity. Herein, a hexagonal rod-shaped ZnO nanoparticles (NP) precursor was prepared using the sol-gel method, which in the presence of varying concentrations of gold (0.005M, 0.01M, and 0.015M) via a greener citrate reduction method afforded a nanocrystalline Au-ZnO nanocomposite. Using which, the visible-light driven photo-degradation kinetics investigation of rhodamine-6G (R6G) dye under blue LED irradiation were carried out. The use of 20 mg 0.015-Au-ZnO completes the degradation of R6G (97.0 %, k = 6.5 X 10−3s−1 at pH 7) within 55 min while 50 mg of 0.015-Au-ZnO catalyst improves the rate of R6G degradation (15 min 97.8 %, k = 14.8 × 10−3 s−1) and it is reusable up to three cycles. The LC-MS spectra of the remains of R6G (after 15 min) identified various low molecular ions (up m/z = 65). Further, the blue-LED assisted anti-cancer studies (MTT assay) using 0.015-Au-ZnO towards human lung cancer cells (A549), breast cancer cells (SKBr3) show high anti-proliferation rate and low cytotoxicity against healthy human embryonic kidney cells (HEK-293) with an IC50 value of 65, 53 and 124 μg/mL respectively. Also, the AO-EB dual staining and DCFH-DA analysis of SKBr3 and A549 cells revealed ROS-mediated cell death via apoptosis. Moreover, plasmid cleavage studies against supercoiled pBR322 DNA result in single-stranded linear DNA without traversing the nicked circular form, suggesting the possible DNA targeting activity of Au-ZnO nanozyme. Thus, the synthesized Au-ZnO nanocomposite shows excellent photocatalytic and biological activity. 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Herein, a hexagonal rod-shaped ZnO nanoparticles (NP) precursor was prepared using the sol-gel method, which in the presence of varying concentrations of gold (0.005M, 0.01M, and 0.015M) via a greener citrate reduction method afforded a nanocrystalline Au-ZnO nanocomposite. Using which, the visible-light driven photo-degradation kinetics investigation of rhodamine-6G (R6G) dye under blue LED irradiation were carried out. The use of 20 mg 0.015-Au-ZnO completes the degradation of R6G (97.0 %, k = 6.5 X 10−3s−1 at pH 7) within 55 min while 50 mg of 0.015-Au-ZnO catalyst improves the rate of R6G degradation (15 min 97.8 %, k = 14.8 × 10−3 s−1) and it is reusable up to three cycles. The LC-MS spectra of the remains of R6G (after 15 min) identified various low molecular ions (up m/z = 65). Further, the blue-LED assisted anti-cancer studies (MTT assay) using 0.015-Au-ZnO towards human lung cancer cells (A549), breast cancer cells (SKBr3) show high anti-proliferation rate and low cytotoxicity against healthy human embryonic kidney cells (HEK-293) with an IC50 value of 65, 53 and 124 μg/mL respectively. Also, the AO-EB dual staining and DCFH-DA analysis of SKBr3 and A549 cells revealed ROS-mediated cell death via apoptosis. Moreover, plasmid cleavage studies against supercoiled pBR322 DNA result in single-stranded linear DNA without traversing the nicked circular form, suggesting the possible DNA targeting activity of Au-ZnO nanozyme. Thus, the synthesized Au-ZnO nanocomposite shows excellent photocatalytic and biological activity. [Display omitted] •A greener citrate reduction method was employed to synthesize plasmonic metal-metal oxide (PMMO) such as Au-ZnO nanocomposites with various concentrations of gold.•Au-ZnO was utilized to perform a blue LED driven Rhodamine-6G dye degradation and 0.015-Au-ZnO is exceedingly good ((98 %, 15 min, 0.014 s−1).•Au-ZnO shows excellent anti-cancer activity against both SKBR3 and A549 cells owing to the in-situ generation of reactive oxygen species (ROS) under blue LED illumination.•EPR studies with TEMPO after LED exposure trap the in situ generated ROS species such as O2−. radical.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.heliyon.2024.e41061</doi><orcidid>https://orcid.org/0000-0003-2879-3092</orcidid><oa>free_for_read</oa></addata></record>
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subjects Acridine orange-ethidium bromide (AO-EB) dual staining
Apoptosis
Plasmide cleavage
Plasmonic metal-metal oxide
Rhodamine-6G Photodegradation
title Blue-LED assisted Photodegradation kinetics of rhodamine-6G dye, enhanced anticancer activity and cleavage of plasmids using Au-ZnO nanocomposite
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