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Hybrid nanocomposite curcumin-capped gold nanoparticle-reduced graphene oxide: Anti-oxidant potency and selective cancer cytotoxicity

Nanotechnology-based antioxidants and therapeutic agents are believed to be the next generation tools to face the ever-increasing cancer mortality rates. Graphene stands as a preferred nano-therapeutic template, due to the advanced properties and cellular interaction mechanisms. Nevertheless, majori...

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Published in:PloS one 2019-05, Vol.14 (5), p.e0216725
Main Authors: Al-Ani, Lina A, Yehye, Wageeh A, Kadir, Farkaad A, Hashim, Najihah M, AlSaadi, Mohammed A, Julkapli, Nurhidayatullaili M, Hsiao, Vincent K S
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container_issue 5
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container_title PloS one
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creator Al-Ani, Lina A
Yehye, Wageeh A
Kadir, Farkaad A
Hashim, Najihah M
AlSaadi, Mohammed A
Julkapli, Nurhidayatullaili M
Hsiao, Vincent K S
description Nanotechnology-based antioxidants and therapeutic agents are believed to be the next generation tools to face the ever-increasing cancer mortality rates. Graphene stands as a preferred nano-therapeutic template, due to the advanced properties and cellular interaction mechanisms. Nevertheless, majority of graphene-based composites suffer from hindered development as efficient cancer therapeutics. Recent nano-toxicology reviews and recommendations emphasize on the preliminary synthetic stages as a crucial element in driving successful applications results. In this study, we present an integrated, green, one-pot hybridization of target-suited raw materials into curcumin-capped gold nanoparticle-conjugated reduced graphene oxide (CAG) nanocomposite, as a prominent anti-oxidant and anti-cancer agent. Distinct from previous studies, the beneficial attributes of curcumin are employed to their fullest extent, such that they perform dual roles of being a natural reducing agent and possessing antioxidant anti-cancer functional moiety. The proposed novel green synthesis approach secured an enhanced structure with dispersed homogenous AuNPs (15.62 ± 4.04 nm) anchored on reduced graphene oxide (rGO) sheets, as evidenced by transmission electron microscopy, surpassing other traditional chemical reductants. On the other hand, safe, non-toxic CAG elevates biological activity and supports biocompatibility. Free radical DPPH inhibition assay revealed CAG antioxidant potential with IC50 (324.1 ± 1.8%) value reduced by half compared to that of traditional citrate-rGO-AuNP nanocomposite (612.1 ± 10.1%), which confirms the amplified multi-potent antioxidant activity. Human colon cancer cell lines (HT-29 and SW-948) showed concentration- and time-dependent cytotoxicity for CAG, as determined by optical microscopy images and WST-8 assay, with relatively low IC50 values (~100 μg/ml), while preserving biocompatibility towards normal human colon (CCD-841) and liver cells (WRL-68), with high selectivity indices (≥ 2.0) at all tested time points. Collectively, our results demonstrate effective green synthesis of CAG nanocomposite, free of additional stabilizing agents, and its bioactivity as an antioxidant and selective anti-colon cancer agent.
doi_str_mv 10.1371/journal.pone.0216725
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one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Al-Ani, Lina A</au><au>Yehye, Wageeh A</au><au>Kadir, Farkaad A</au><au>Hashim, Najihah M</au><au>AlSaadi, Mohammed A</au><au>Julkapli, Nurhidayatullaili M</au><au>Hsiao, Vincent K S</au><au>Mishra, Yogendra Kumar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hybrid nanocomposite curcumin-capped gold nanoparticle-reduced graphene oxide: Anti-oxidant potency and selective cancer cytotoxicity</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2019-05-14</date><risdate>2019</risdate><volume>14</volume><issue>5</issue><spage>e0216725</spage><pages>e0216725-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Nanotechnology-based antioxidants and therapeutic agents are believed to be the next generation tools to face the ever-increasing cancer mortality rates. Graphene stands as a preferred nano-therapeutic template, due to the advanced properties and cellular interaction mechanisms. Nevertheless, majority of graphene-based composites suffer from hindered development as efficient cancer therapeutics. Recent nano-toxicology reviews and recommendations emphasize on the preliminary synthetic stages as a crucial element in driving successful applications results. In this study, we present an integrated, green, one-pot hybridization of target-suited raw materials into curcumin-capped gold nanoparticle-conjugated reduced graphene oxide (CAG) nanocomposite, as a prominent anti-oxidant and anti-cancer agent. Distinct from previous studies, the beneficial attributes of curcumin are employed to their fullest extent, such that they perform dual roles of being a natural reducing agent and possessing antioxidant anti-cancer functional moiety. The proposed novel green synthesis approach secured an enhanced structure with dispersed homogenous AuNPs (15.62 ± 4.04 nm) anchored on reduced graphene oxide (rGO) sheets, as evidenced by transmission electron microscopy, surpassing other traditional chemical reductants. On the other hand, safe, non-toxic CAG elevates biological activity and supports biocompatibility. Free radical DPPH inhibition assay revealed CAG antioxidant potential with IC50 (324.1 ± 1.8%) value reduced by half compared to that of traditional citrate-rGO-AuNP nanocomposite (612.1 ± 10.1%), which confirms the amplified multi-potent antioxidant activity. Human colon cancer cell lines (HT-29 and SW-948) showed concentration- and time-dependent cytotoxicity for CAG, as determined by optical microscopy images and WST-8 assay, with relatively low IC50 values (~100 μg/ml), while preserving biocompatibility towards normal human colon (CCD-841) and liver cells (WRL-68), with high selectivity indices (≥ 2.0) at all tested time points. Collectively, our results demonstrate effective green synthesis of CAG nanocomposite, free of additional stabilizing agents, and its bioactivity as an antioxidant and selective anti-colon cancer agent.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31086406</pmid><doi>10.1371/journal.pone.0216725</doi><tpages>e0216725</tpages><orcidid>https://orcid.org/0000-0003-1543-9887</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
ispartof PloS one, 2019-05, Vol.14 (5), p.e0216725
issn 1932-6203
1932-6203
language eng
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source Publicly Available Content Database; PubMed Central
subjects Anticancer properties
Antineoplastic Agents - chemistry
Antineoplastic Agents - pharmacology
Antioxidants
Antioxidants (Nutrients)
Antioxidants - chemistry
Antioxidants - pharmacology
Apoptosis
Biocompatibility
Biological activity
Biology and Life Sciences
Cancer
Cancer therapies
Cancer treatment
Catalysis
Cell cycle
Cell Line, Tumor
Cell Survival - drug effects
Chemical compounds
Citric acid
Colon
Colon cancer
Colorectal cancer
Curcumin
Curcumin - chemistry
Curcumin - pharmacology
Cytotoxicity
Drug development
Electron microscopy
Engineering and Technology
Free radicals
Gold
Gold - chemistry
Graphene
Graphite
Graphite - chemistry
Health aspects
Hepatocytes
Humans
Hybridization
Medical research
Medicine and Health Sciences
Metal Nanoparticles - chemistry
Microscopy
Models, Molecular
Molecular Conformation
Nanocomposites
Nanocomposites - chemistry
Nanomaterials
Nanoparticles
Nanotechnology
Optical microscopy
Organic chemistry
Oxidation-Reduction
Pandas
Patient outcomes
Pharmacology
Physical Sciences
Raw materials
Reagents
Reducing agents
Selectivity
Synthesis
Therapeutics
Time dependence
Toxicity
Toxicology
Transmission electron microscopy
Trinucleotide repeats
Tumor cell lines
title Hybrid nanocomposite curcumin-capped gold nanoparticle-reduced graphene oxide: Anti-oxidant potency and selective cancer cytotoxicity
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