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Synergistic Cytotoxicity Of Shikonin‐Silver Nanoparticles As An Opportunity For Lung Cancer
The combined action of shikonin and silver nanoparticles (AgNPs) for apoptosis in human cancer cells has not been elucidated. Hence, we investigated the synergistic combinatorial effect of shikonin and AgNPs in human lung cancer cells. Shikonin was used as a reducing and capping agent for AgNPs synt...
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Published in: | Journal of labelled compounds & radiopharmaceuticals 2020-01, Vol.63 (1), p.25-32 |
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description | The combined action of shikonin and silver nanoparticles (AgNPs) for apoptosis in human cancer cells has not been elucidated. Hence, we investigated the synergistic combinatorial effect of shikonin and AgNPs in human lung cancer cells. Shikonin was used as a reducing and capping agent for AgNPs synthesis as a green method avoiding the hazards of chemical methods. Radiolabeling of shikonin‐AgNPs with radioactive iodine forming [131I]I‐Shikonin‐AgNPs was carried out to enable the intracellular tracking of NPs. The antitumor effect of a combined treatment (shikonin‐AgNPs) was evaluated using tissue culture assay. The 50% inhibitory concentration (IC50) of SHK‐AgNPs on A549 cells after 24 hours determined by an MTT assay is 2.4 ± 0.11 μg/mL. As a deduction, this study revealed that the combination of shikonin and AgNPs treatment significantly inhibited cell viability and proliferation of A549 cells (human lung carcinoma cell line) with a great potential than the monotherapy.
A shikonin silver nanoparticles were synthesized, characterized and tested in‐vitro for there synergestic cytotoxic effect against human lung carcinoma cell line and then tracked in‐vivo to study its biodistribution and affinity to lung cell and showed high affinity to lung tissues. so, shikonin Ag‐NPs may be considered as an opportunity to lung cancer. |
doi_str_mv | 10.1002/jlcr.3818 |
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A shikonin silver nanoparticles were synthesized, characterized and tested in‐vitro for there synergestic cytotoxic effect against human lung carcinoma cell line and then tracked in‐vivo to study its biodistribution and affinity to lung cell and showed high affinity to lung tissues. so, shikonin Ag‐NPs may be considered as an opportunity to lung cancer.</description><identifier>ISSN: 0362-4803</identifier><identifier>ISSN: 1099-1344</identifier><identifier>EISSN: 1099-1344</identifier><identifier>DOI: 10.1002/jlcr.3818</identifier><identifier>PMID: 31785206</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>A549 Cells ; Anticancer properties ; Antineoplastic Agents - chemical synthesis ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - pharmacology ; Antitumor activity ; Apoptosis ; Cell culture ; Cell proliferation ; Cell Proliferation - drug effects ; Cell Survival - drug effects ; Cell viability ; Combinatorial analysis ; Cytotoxicity ; Deduction ; Drug Synergism ; Hazard mitigation ; Humans ; Iodine ; Lung cancer ; Lung carcinoma ; Lung Neoplasms - drug therapy ; Lung Neoplasms - pathology ; Metal Nanoparticles - chemistry ; Nanoparticles ; Naphthoquinones - chemistry ; Naphthoquinones - pharmacology ; Organic chemistry ; radiolabeling ; Radiolabelling ; Shikonin ; Silver ; Silver - chemistry ; Silver - pharmacology ; silver nanoparticle ; Tissue culture ; Toxicity</subject><ispartof>Journal of labelled compounds & radiopharmaceuticals, 2020-01, Vol.63 (1), p.25-32</ispartof><rights>2019 John Wiley & Sons, Ltd.</rights><rights>2020 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3538-d01e047e2dafcc63a2e3ef3e962cbf5a716465d802ca88b58b64f19c3060b0f73</citedby><cites>FETCH-LOGICAL-c3538-d01e047e2dafcc63a2e3ef3e962cbf5a716465d802ca88b58b64f19c3060b0f73</cites><orcidid>0000-0001-6778-7424 ; 0000-0001-7095-5978 ; 0000-0001-5377-9124</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31785206$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fayez, Hend</creatorcontrib><creatorcontrib>El‐Motaleb, Mohamed Abd</creatorcontrib><creatorcontrib>Selim, Adli Abdullah</creatorcontrib><title>Synergistic Cytotoxicity Of Shikonin‐Silver Nanoparticles As An Opportunity For Lung Cancer</title><title>Journal of labelled compounds & radiopharmaceuticals</title><addtitle>J Labelled Comp Radiopharm</addtitle><description>The combined action of shikonin and silver nanoparticles (AgNPs) for apoptosis in human cancer cells has not been elucidated. Hence, we investigated the synergistic combinatorial effect of shikonin and AgNPs in human lung cancer cells. Shikonin was used as a reducing and capping agent for AgNPs synthesis as a green method avoiding the hazards of chemical methods. Radiolabeling of shikonin‐AgNPs with radioactive iodine forming [131I]I‐Shikonin‐AgNPs was carried out to enable the intracellular tracking of NPs. The antitumor effect of a combined treatment (shikonin‐AgNPs) was evaluated using tissue culture assay. The 50% inhibitory concentration (IC50) of SHK‐AgNPs on A549 cells after 24 hours determined by an MTT assay is 2.4 ± 0.11 μg/mL. As a deduction, this study revealed that the combination of shikonin and AgNPs treatment significantly inhibited cell viability and proliferation of A549 cells (human lung carcinoma cell line) with a great potential than the monotherapy.
A shikonin silver nanoparticles were synthesized, characterized and tested in‐vitro for there synergestic cytotoxic effect against human lung carcinoma cell line and then tracked in‐vivo to study its biodistribution and affinity to lung cell and showed high affinity to lung tissues. so, shikonin Ag‐NPs may be considered as an opportunity to lung cancer.</description><subject>A549 Cells</subject><subject>Anticancer properties</subject><subject>Antineoplastic Agents - chemical synthesis</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antitumor activity</subject><subject>Apoptosis</subject><subject>Cell culture</subject><subject>Cell proliferation</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Cell viability</subject><subject>Combinatorial analysis</subject><subject>Cytotoxicity</subject><subject>Deduction</subject><subject>Drug Synergism</subject><subject>Hazard mitigation</subject><subject>Humans</subject><subject>Iodine</subject><subject>Lung cancer</subject><subject>Lung carcinoma</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - pathology</subject><subject>Metal Nanoparticles - chemistry</subject><subject>Nanoparticles</subject><subject>Naphthoquinones - chemistry</subject><subject>Naphthoquinones - pharmacology</subject><subject>Organic chemistry</subject><subject>radiolabeling</subject><subject>Radiolabelling</subject><subject>Shikonin</subject><subject>Silver</subject><subject>Silver - chemistry</subject><subject>Silver - pharmacology</subject><subject>silver nanoparticle</subject><subject>Tissue culture</subject><subject>Toxicity</subject><issn>0362-4803</issn><issn>1099-1344</issn><issn>1099-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp10MFO3DAQBmCrAnUX6KEvgCJxKYfA2E4c54iiLi1asVIXjihyvM7iJWsHO2nJrY_AM_IkdVjaA1IlS3PwN79GP0KfMZxhAHK-aaQ7oxzzD2iKIc9jTJNkD02BMhInHOgEHXi_AQh_SfIRTSjOeEqATdHdcjDKrbXvtIyKobOdfdJSd0O0qKPlvX6wRpuX389L3fxULroWxrbCBdwoH12EZ6JF21rX9WZcmlkXzXuzjgphpHJHaL8WjVef3uYhup19vSm-xfPF5ffiYh5LmlIerwArSDJFVqKWklFBFFU1VTkjsqpTkWGWsHTFgUjBeZXyiiU1ziUFBhXUGT1EX3a5rbOPvfJdudVeqqYRRtnel4QSoHkGLA_05B3d2N6ZcF1QKWFAMWVBne6UdNZ7p-qydXor3FBiKMfOy7Hzcuw82OO3xL7aqtU_-bfkAM534Jdu1PD_pPJqXvx4jfwDKfqMiA</recordid><startdate>202001</startdate><enddate>202001</enddate><creator>Fayez, Hend</creator><creator>El‐Motaleb, Mohamed Abd</creator><creator>Selim, Adli Abdullah</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6778-7424</orcidid><orcidid>https://orcid.org/0000-0001-7095-5978</orcidid><orcidid>https://orcid.org/0000-0001-5377-9124</orcidid></search><sort><creationdate>202001</creationdate><title>Synergistic Cytotoxicity Of Shikonin‐Silver Nanoparticles As An Opportunity For Lung Cancer</title><author>Fayez, Hend ; El‐Motaleb, Mohamed Abd ; Selim, Adli Abdullah</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3538-d01e047e2dafcc63a2e3ef3e962cbf5a716465d802ca88b58b64f19c3060b0f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>A549 Cells</topic><topic>Anticancer properties</topic><topic>Antineoplastic Agents - chemical synthesis</topic><topic>Antineoplastic Agents - chemistry</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antitumor activity</topic><topic>Apoptosis</topic><topic>Cell culture</topic><topic>Cell proliferation</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>Cell viability</topic><topic>Combinatorial analysis</topic><topic>Cytotoxicity</topic><topic>Deduction</topic><topic>Drug Synergism</topic><topic>Hazard mitigation</topic><topic>Humans</topic><topic>Iodine</topic><topic>Lung cancer</topic><topic>Lung carcinoma</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - pathology</topic><topic>Metal Nanoparticles - chemistry</topic><topic>Nanoparticles</topic><topic>Naphthoquinones - chemistry</topic><topic>Naphthoquinones - pharmacology</topic><topic>Organic chemistry</topic><topic>radiolabeling</topic><topic>Radiolabelling</topic><topic>Shikonin</topic><topic>Silver</topic><topic>Silver - chemistry</topic><topic>Silver - pharmacology</topic><topic>silver nanoparticle</topic><topic>Tissue culture</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fayez, Hend</creatorcontrib><creatorcontrib>El‐Motaleb, Mohamed Abd</creatorcontrib><creatorcontrib>Selim, Adli Abdullah</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of labelled compounds & radiopharmaceuticals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fayez, Hend</au><au>El‐Motaleb, Mohamed Abd</au><au>Selim, Adli Abdullah</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synergistic Cytotoxicity Of Shikonin‐Silver Nanoparticles As An Opportunity For Lung Cancer</atitle><jtitle>Journal of labelled compounds & radiopharmaceuticals</jtitle><addtitle>J Labelled Comp Radiopharm</addtitle><date>2020-01</date><risdate>2020</risdate><volume>63</volume><issue>1</issue><spage>25</spage><epage>32</epage><pages>25-32</pages><issn>0362-4803</issn><issn>1099-1344</issn><eissn>1099-1344</eissn><abstract>The combined action of shikonin and silver nanoparticles (AgNPs) for apoptosis in human cancer cells has not been elucidated. Hence, we investigated the synergistic combinatorial effect of shikonin and AgNPs in human lung cancer cells. Shikonin was used as a reducing and capping agent for AgNPs synthesis as a green method avoiding the hazards of chemical methods. Radiolabeling of shikonin‐AgNPs with radioactive iodine forming [131I]I‐Shikonin‐AgNPs was carried out to enable the intracellular tracking of NPs. The antitumor effect of a combined treatment (shikonin‐AgNPs) was evaluated using tissue culture assay. The 50% inhibitory concentration (IC50) of SHK‐AgNPs on A549 cells after 24 hours determined by an MTT assay is 2.4 ± 0.11 μg/mL. As a deduction, this study revealed that the combination of shikonin and AgNPs treatment significantly inhibited cell viability and proliferation of A549 cells (human lung carcinoma cell line) with a great potential than the monotherapy.
A shikonin silver nanoparticles were synthesized, characterized and tested in‐vitro for there synergestic cytotoxic effect against human lung carcinoma cell line and then tracked in‐vivo to study its biodistribution and affinity to lung cell and showed high affinity to lung tissues. so, shikonin Ag‐NPs may be considered as an opportunity to lung cancer.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31785206</pmid><doi>10.1002/jlcr.3818</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-6778-7424</orcidid><orcidid>https://orcid.org/0000-0001-7095-5978</orcidid><orcidid>https://orcid.org/0000-0001-5377-9124</orcidid></addata></record> |
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subjects | A549 Cells Anticancer properties Antineoplastic Agents - chemical synthesis Antineoplastic Agents - chemistry Antineoplastic Agents - pharmacology Antitumor activity Apoptosis Cell culture Cell proliferation Cell Proliferation - drug effects Cell Survival - drug effects Cell viability Combinatorial analysis Cytotoxicity Deduction Drug Synergism Hazard mitigation Humans Iodine Lung cancer Lung carcinoma Lung Neoplasms - drug therapy Lung Neoplasms - pathology Metal Nanoparticles - chemistry Nanoparticles Naphthoquinones - chemistry Naphthoquinones - pharmacology Organic chemistry radiolabeling Radiolabelling Shikonin Silver Silver - chemistry Silver - pharmacology silver nanoparticle Tissue culture Toxicity |
title | Synergistic Cytotoxicity Of Shikonin‐Silver Nanoparticles As An Opportunity For Lung Cancer |
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