Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells

Zinc oxide nanoparticles are used increasingly as antimicrobial and therapeutic agents, and the addition of metal ions such as silver may improve their potent cytotoxicity. However, there have been concerns about safety. In this work, we investigated the cytotoxic activity of newly synthesized silve...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Rad, Mina Mahdavi [verfasserIn] Najafzadeh, Nowruz [verfasserIn] Tata, Nasrin [verfasserIn] Jafari, Alireza [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2018

Schlagwörter:	cytotoxicity ZnO nanoparticles Ag-ZnO nanocomposites cell cycle arrest

Übergeordnetes Werk:	Enthalten in: Pharmaceutical chemistry journal - Dordrecht [u.a.] : Springer Science + Business Media B.V, 1967, 52(2018), 2 vom: Mai, Seite 112-116
Übergeordnetes Werk:	volume:52 ; year:2018 ; number:2 ; month:05 ; pages:112-116

Links:	Volltext

DOI / URN:	10.1007/s11094-018-1774-9

Katalog-ID:	SPR016542681

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matchkey_str	article:15739031:2018----::gnnncmoiecueyooiiynidcclcceretnuagsr
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publishDate	2018
allfields	10.1007/s11094-018-1774-9 doi (DE-627)SPR016542681 (SPR)s11094-018-1774-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.40 bkl Rad, Mina Mahdavi verfasserin aut Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Zinc oxide nanoparticles are used increasingly as antimicrobial and therapeutic agents, and the addition of metal ions such as silver may improve their potent cytotoxicity. However, there have been concerns about safety. In this work, we investigated the cytotoxic activity of newly synthesized silver/zinc oxide nanocomposites (Ag-ZnO NCs) versus ZnO nanoparticles (NPs) against human melanoma (A375) and gastric carcinoma (AGS). The cytotoxicity of Ag-ZnO NCs versus ZnO NPs was evaluated by cell viability assays and the cell cycle analyses were performed by flow cytometry using DAPI staining. Both ZnO NPs and Ag-ZnO NCs significantly reduced cell viability in a dose-dependent manner. We found that Ag-ZnO NCs cytotoxicity was lower than that of ZnO NPs in the same concentration range. Furthermore, the cytotoxicity caused by Ag-ZnO NCs and ZnO induced the accumulation of melanoma cells in S phase and gastric cancer cells in G2/M phase. It was concluded that Ag-ZnO NCs were less toxic than ZnO NPs. This approach provides a rational basis for evaluating the potential harm of ZnO NPs and Ag-ZnO NCs as food packaging materials and cancer therapy agents. cytotoxicity (dpeaa)DE-He213 ZnO nanoparticles (dpeaa)DE-He213 Ag-ZnO nanocomposites (dpeaa)DE-He213 cell cycle arrest (dpeaa)DE-He213 Najafzadeh, Nowruz verfasserin aut Tata, Nasrin verfasserin aut Jafari, Alireza verfasserin aut Enthalten in Pharmaceutical chemistry journal Dordrecht [u.a.] : Springer Science + Business Media B.V, 1967 52(2018), 2 vom: Mai, Seite 112-116 (DE-627)325700621 (DE-600)2039418-4 1573-9031 nnns volume:52 year:2018 number:2 month:05 pages:112-116 https://dx.doi.org/10.1007/s11094-018-1774-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.40 ASE AR 52 2018 2 05 112-116
spelling	10.1007/s11094-018-1774-9 doi (DE-627)SPR016542681 (SPR)s11094-018-1774-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.40 bkl Rad, Mina Mahdavi verfasserin aut Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Zinc oxide nanoparticles are used increasingly as antimicrobial and therapeutic agents, and the addition of metal ions such as silver may improve their potent cytotoxicity. However, there have been concerns about safety. In this work, we investigated the cytotoxic activity of newly synthesized silver/zinc oxide nanocomposites (Ag-ZnO NCs) versus ZnO nanoparticles (NPs) against human melanoma (A375) and gastric carcinoma (AGS). The cytotoxicity of Ag-ZnO NCs versus ZnO NPs was evaluated by cell viability assays and the cell cycle analyses were performed by flow cytometry using DAPI staining. Both ZnO NPs and Ag-ZnO NCs significantly reduced cell viability in a dose-dependent manner. We found that Ag-ZnO NCs cytotoxicity was lower than that of ZnO NPs in the same concentration range. Furthermore, the cytotoxicity caused by Ag-ZnO NCs and ZnO induced the accumulation of melanoma cells in S phase and gastric cancer cells in G2/M phase. It was concluded that Ag-ZnO NCs were less toxic than ZnO NPs. This approach provides a rational basis for evaluating the potential harm of ZnO NPs and Ag-ZnO NCs as food packaging materials and cancer therapy agents. cytotoxicity (dpeaa)DE-He213 ZnO nanoparticles (dpeaa)DE-He213 Ag-ZnO nanocomposites (dpeaa)DE-He213 cell cycle arrest (dpeaa)DE-He213 Najafzadeh, Nowruz verfasserin aut Tata, Nasrin verfasserin aut Jafari, Alireza verfasserin aut Enthalten in Pharmaceutical chemistry journal Dordrecht [u.a.] : Springer Science + Business Media B.V, 1967 52(2018), 2 vom: Mai, Seite 112-116 (DE-627)325700621 (DE-600)2039418-4 1573-9031 nnns volume:52 year:2018 number:2 month:05 pages:112-116 https://dx.doi.org/10.1007/s11094-018-1774-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.40 ASE AR 52 2018 2 05 112-116
allfields_unstemmed	10.1007/s11094-018-1774-9 doi (DE-627)SPR016542681 (SPR)s11094-018-1774-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.40 bkl Rad, Mina Mahdavi verfasserin aut Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Zinc oxide nanoparticles are used increasingly as antimicrobial and therapeutic agents, and the addition of metal ions such as silver may improve their potent cytotoxicity. However, there have been concerns about safety. In this work, we investigated the cytotoxic activity of newly synthesized silver/zinc oxide nanocomposites (Ag-ZnO NCs) versus ZnO nanoparticles (NPs) against human melanoma (A375) and gastric carcinoma (AGS). The cytotoxicity of Ag-ZnO NCs versus ZnO NPs was evaluated by cell viability assays and the cell cycle analyses were performed by flow cytometry using DAPI staining. Both ZnO NPs and Ag-ZnO NCs significantly reduced cell viability in a dose-dependent manner. We found that Ag-ZnO NCs cytotoxicity was lower than that of ZnO NPs in the same concentration range. Furthermore, the cytotoxicity caused by Ag-ZnO NCs and ZnO induced the accumulation of melanoma cells in S phase and gastric cancer cells in G2/M phase. It was concluded that Ag-ZnO NCs were less toxic than ZnO NPs. This approach provides a rational basis for evaluating the potential harm of ZnO NPs and Ag-ZnO NCs as food packaging materials and cancer therapy agents. cytotoxicity (dpeaa)DE-He213 ZnO nanoparticles (dpeaa)DE-He213 Ag-ZnO nanocomposites (dpeaa)DE-He213 cell cycle arrest (dpeaa)DE-He213 Najafzadeh, Nowruz verfasserin aut Tata, Nasrin verfasserin aut Jafari, Alireza verfasserin aut Enthalten in Pharmaceutical chemistry journal Dordrecht [u.a.] : Springer Science + Business Media B.V, 1967 52(2018), 2 vom: Mai, Seite 112-116 (DE-627)325700621 (DE-600)2039418-4 1573-9031 nnns volume:52 year:2018 number:2 month:05 pages:112-116 https://dx.doi.org/10.1007/s11094-018-1774-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.40 ASE AR 52 2018 2 05 112-116
allfieldsGer	10.1007/s11094-018-1774-9 doi (DE-627)SPR016542681 (SPR)s11094-018-1774-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.40 bkl Rad, Mina Mahdavi verfasserin aut Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Zinc oxide nanoparticles are used increasingly as antimicrobial and therapeutic agents, and the addition of metal ions such as silver may improve their potent cytotoxicity. However, there have been concerns about safety. In this work, we investigated the cytotoxic activity of newly synthesized silver/zinc oxide nanocomposites (Ag-ZnO NCs) versus ZnO nanoparticles (NPs) against human melanoma (A375) and gastric carcinoma (AGS). The cytotoxicity of Ag-ZnO NCs versus ZnO NPs was evaluated by cell viability assays and the cell cycle analyses were performed by flow cytometry using DAPI staining. Both ZnO NPs and Ag-ZnO NCs significantly reduced cell viability in a dose-dependent manner. We found that Ag-ZnO NCs cytotoxicity was lower than that of ZnO NPs in the same concentration range. Furthermore, the cytotoxicity caused by Ag-ZnO NCs and ZnO induced the accumulation of melanoma cells in S phase and gastric cancer cells in G2/M phase. It was concluded that Ag-ZnO NCs were less toxic than ZnO NPs. This approach provides a rational basis for evaluating the potential harm of ZnO NPs and Ag-ZnO NCs as food packaging materials and cancer therapy agents. cytotoxicity (dpeaa)DE-He213 ZnO nanoparticles (dpeaa)DE-He213 Ag-ZnO nanocomposites (dpeaa)DE-He213 cell cycle arrest (dpeaa)DE-He213 Najafzadeh, Nowruz verfasserin aut Tata, Nasrin verfasserin aut Jafari, Alireza verfasserin aut Enthalten in Pharmaceutical chemistry journal Dordrecht [u.a.] : Springer Science + Business Media B.V, 1967 52(2018), 2 vom: Mai, Seite 112-116 (DE-627)325700621 (DE-600)2039418-4 1573-9031 nnns volume:52 year:2018 number:2 month:05 pages:112-116 https://dx.doi.org/10.1007/s11094-018-1774-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.40 ASE AR 52 2018 2 05 112-116
allfieldsSound	10.1007/s11094-018-1774-9 doi (DE-627)SPR016542681 (SPR)s11094-018-1774-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.40 bkl Rad, Mina Mahdavi verfasserin aut Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Zinc oxide nanoparticles are used increasingly as antimicrobial and therapeutic agents, and the addition of metal ions such as silver may improve their potent cytotoxicity. However, there have been concerns about safety. In this work, we investigated the cytotoxic activity of newly synthesized silver/zinc oxide nanocomposites (Ag-ZnO NCs) versus ZnO nanoparticles (NPs) against human melanoma (A375) and gastric carcinoma (AGS). The cytotoxicity of Ag-ZnO NCs versus ZnO NPs was evaluated by cell viability assays and the cell cycle analyses were performed by flow cytometry using DAPI staining. Both ZnO NPs and Ag-ZnO NCs significantly reduced cell viability in a dose-dependent manner. We found that Ag-ZnO NCs cytotoxicity was lower than that of ZnO NPs in the same concentration range. Furthermore, the cytotoxicity caused by Ag-ZnO NCs and ZnO induced the accumulation of melanoma cells in S phase and gastric cancer cells in G2/M phase. It was concluded that Ag-ZnO NCs were less toxic than ZnO NPs. This approach provides a rational basis for evaluating the potential harm of ZnO NPs and Ag-ZnO NCs as food packaging materials and cancer therapy agents. cytotoxicity (dpeaa)DE-He213 ZnO nanoparticles (dpeaa)DE-He213 Ag-ZnO nanocomposites (dpeaa)DE-He213 cell cycle arrest (dpeaa)DE-He213 Najafzadeh, Nowruz verfasserin aut Tata, Nasrin verfasserin aut Jafari, Alireza verfasserin aut Enthalten in Pharmaceutical chemistry journal Dordrecht [u.a.] : Springer Science + Business Media B.V, 1967 52(2018), 2 vom: Mai, Seite 112-116 (DE-627)325700621 (DE-600)2039418-4 1573-9031 nnns volume:52 year:2018 number:2 month:05 pages:112-116 https://dx.doi.org/10.1007/s11094-018-1774-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA SSG-OPC-PHA SSG-OPC-ASE GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.40 ASE AR 52 2018 2 05 112-116
language	English
source	Enthalten in Pharmaceutical chemistry journal 52(2018), 2 vom: Mai, Seite 112-116 volume:52 year:2018 number:2 month:05 pages:112-116
sourceStr	Enthalten in Pharmaceutical chemistry journal 52(2018), 2 vom: Mai, Seite 112-116 volume:52 year:2018 number:2 month:05 pages:112-116
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	cytotoxicity ZnO nanoparticles Ag-ZnO nanocomposites cell cycle arrest
dewey-raw	610
isfreeaccess_bool	false
container_title	Pharmaceutical chemistry journal
authorswithroles_txt_mv	Rad, Mina Mahdavi @@aut@@ Najafzadeh, Nowruz @@aut@@ Tata, Nasrin @@aut@@ Jafari, Alireza @@aut@@
publishDateDaySort_date	2018-05-01T00:00:00Z
hierarchy_top_id	325700621
dewey-sort	3610
id	SPR016542681
language_de	englisch
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author	Rad, Mina Mahdavi
spellingShingle	Rad, Mina Mahdavi ddc 610 bkl 44.40 misc cytotoxicity misc ZnO nanoparticles misc Ag-ZnO nanocomposites misc cell cycle arrest Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells
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topic_title	610 ASE 44.40 bkl Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells cytotoxicity (dpeaa)DE-He213 ZnO nanoparticles (dpeaa)DE-He213 Ag-ZnO nanocomposites (dpeaa)DE-He213 cell cycle arrest (dpeaa)DE-He213
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title	Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells
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title_full	Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells
author_sort	Rad, Mina Mahdavi
journal	Pharmaceutical chemistry journal
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author_browse	Rad, Mina Mahdavi Najafzadeh, Nowruz Tata, Nasrin Jafari, Alireza
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title_sort	ag – zno nanocomposites cause cytotoxicity and induce cell cycle arrest in human gastric and melanoma cancer cells
title_auth	Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells
abstract	Zinc oxide nanoparticles are used increasingly as antimicrobial and therapeutic agents, and the addition of metal ions such as silver may improve their potent cytotoxicity. However, there have been concerns about safety. In this work, we investigated the cytotoxic activity of newly synthesized silver/zinc oxide nanocomposites (Ag-ZnO NCs) versus ZnO nanoparticles (NPs) against human melanoma (A375) and gastric carcinoma (AGS). The cytotoxicity of Ag-ZnO NCs versus ZnO NPs was evaluated by cell viability assays and the cell cycle analyses were performed by flow cytometry using DAPI staining. Both ZnO NPs and Ag-ZnO NCs significantly reduced cell viability in a dose-dependent manner. We found that Ag-ZnO NCs cytotoxicity was lower than that of ZnO NPs in the same concentration range. Furthermore, the cytotoxicity caused by Ag-ZnO NCs and ZnO induced the accumulation of melanoma cells in S phase and gastric cancer cells in G2/M phase. It was concluded that Ag-ZnO NCs were less toxic than ZnO NPs. This approach provides a rational basis for evaluating the potential harm of ZnO NPs and Ag-ZnO NCs as food packaging materials and cancer therapy agents.
abstractGer	Zinc oxide nanoparticles are used increasingly as antimicrobial and therapeutic agents, and the addition of metal ions such as silver may improve their potent cytotoxicity. However, there have been concerns about safety. In this work, we investigated the cytotoxic activity of newly synthesized silver/zinc oxide nanocomposites (Ag-ZnO NCs) versus ZnO nanoparticles (NPs) against human melanoma (A375) and gastric carcinoma (AGS). The cytotoxicity of Ag-ZnO NCs versus ZnO NPs was evaluated by cell viability assays and the cell cycle analyses were performed by flow cytometry using DAPI staining. Both ZnO NPs and Ag-ZnO NCs significantly reduced cell viability in a dose-dependent manner. We found that Ag-ZnO NCs cytotoxicity was lower than that of ZnO NPs in the same concentration range. Furthermore, the cytotoxicity caused by Ag-ZnO NCs and ZnO induced the accumulation of melanoma cells in S phase and gastric cancer cells in G2/M phase. It was concluded that Ag-ZnO NCs were less toxic than ZnO NPs. This approach provides a rational basis for evaluating the potential harm of ZnO NPs and Ag-ZnO NCs as food packaging materials and cancer therapy agents.
abstract_unstemmed	Zinc oxide nanoparticles are used increasingly as antimicrobial and therapeutic agents, and the addition of metal ions such as silver may improve their potent cytotoxicity. However, there have been concerns about safety. In this work, we investigated the cytotoxic activity of newly synthesized silver/zinc oxide nanocomposites (Ag-ZnO NCs) versus ZnO nanoparticles (NPs) against human melanoma (A375) and gastric carcinoma (AGS). The cytotoxicity of Ag-ZnO NCs versus ZnO NPs was evaluated by cell viability assays and the cell cycle analyses were performed by flow cytometry using DAPI staining. Both ZnO NPs and Ag-ZnO NCs significantly reduced cell viability in a dose-dependent manner. We found that Ag-ZnO NCs cytotoxicity was lower than that of ZnO NPs in the same concentration range. Furthermore, the cytotoxicity caused by Ag-ZnO NCs and ZnO induced the accumulation of melanoma cells in S phase and gastric cancer cells in G2/M phase. It was concluded that Ag-ZnO NCs were less toxic than ZnO NPs. This approach provides a rational basis for evaluating the potential harm of ZnO NPs and Ag-ZnO NCs as food packaging materials and cancer therapy agents.
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title_short	Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells
url	https://dx.doi.org/10.1007/s11094-018-1774-9
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author2	Najafzadeh, Nowruz Tata, Nasrin Jafari, Alireza
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doi_str	10.1007/s11094-018-1774-9
up_date	2024-07-03T23:39:18.767Z
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Ag – ZnO Nanocomposites Cause Cytotoxicity and Induce Cell Cycle Arrest in Human Gastric and Melanoma Cancer Cells

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