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Human plasma protein corona decreases the toxicity of pillar-layer metal organic framework
This scenario was designed to investigate the protein corona pattern on the pillar-layer surface of a Cu-based metal–organic framework (MOF) in human plasma. The [Cu(L)(L / )].1.3DMA (MOF-1) {L = 4, 4 / -bipyridine and L / = 5-aminoisophthalic acid}, was synthesized through the sonochemical irradia...
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Published in: | Scientific reports 2020-09, Vol.10 (1), p.14569, Article 14569 |
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creator | Jafari, Samira Izadi, Zhila Alaei, Loghman Jaymand, Mehdi Samadian, Hadi Kashani, Vali ollah Derakhshankhah, Hossein Hayati, Payam Noori, Foad Mansouri, Kamran Moakedi, Faezeh Janczak, Jan Soltanian Fard, Mohammad Jaafar Fayaz bakhsh, Nozar |
description | This scenario was designed to investigate the protein corona pattern on the pillar-layer surface of a Cu-based metal–organic framework (MOF) in human plasma. The [Cu(L)(L
/
)].1.3DMA (MOF-1) {L = 4, 4
/
-bipyridine and L
/
= 5-aminoisophthalic acid}, was synthesized through the sonochemical irradiation approach as well as characterized by various techniques like scanning electron microscopy, Fourier-transform infrared spectroscopy, X-ray powder diffraction and single-crystal X-ray diffraction. The space group was determined to be an orthorhombic space group (
Pbam
) by single-crystal X-ray diffraction. Single-crystal X-ray analyses on MOF-1 showed that Cu
+2
ion was 6-coordinated. Besides, to study and clarify interactions between MOFs and biological milieu, human whole blood plasma was selected as a model. Fluorescence spectroscopy and SDS-PAGE techniques were employed to explore quantitative and qualitative in situ characterization of protein corona as well. Furthermore, cell viability in a cancerous cell lines was evaluated by MTT assay in the presence and absence of the corona. The results from SDS-PAGE illustrated that the most adsorbed quantity among plasma proteins belongs to fibrinogen (α, β and γ chains), and this protein showed the maximum frequency on the MOF-1s surface, so the possible interactions of MOF-1s with fibrinogen also studied using fluorescence spectroscopy and corresponding data were plotted. According to the obtained data from MTT assay, these structures have concentration-dependent toxicity. In brief, based on the obtained data in the current study, the designed MOF can be introduced as a new desirable carrier for drug/gen delivery after further prerequisite assessments. |
doi_str_mv | 10.1038/s41598-020-71170-z |
format | article |
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/
)].1.3DMA (MOF-1) {L = 4, 4
/
-bipyridine and L
/
= 5-aminoisophthalic acid}, was synthesized through the sonochemical irradiation approach as well as characterized by various techniques like scanning electron microscopy, Fourier-transform infrared spectroscopy, X-ray powder diffraction and single-crystal X-ray diffraction. The space group was determined to be an orthorhombic space group (
Pbam
) by single-crystal X-ray diffraction. Single-crystal X-ray analyses on MOF-1 showed that Cu
+2
ion was 6-coordinated. Besides, to study and clarify interactions between MOFs and biological milieu, human whole blood plasma was selected as a model. Fluorescence spectroscopy and SDS-PAGE techniques were employed to explore quantitative and qualitative in situ characterization of protein corona as well. Furthermore, cell viability in a cancerous cell lines was evaluated by MTT assay in the presence and absence of the corona. The results from SDS-PAGE illustrated that the most adsorbed quantity among plasma proteins belongs to fibrinogen (α, β and γ chains), and this protein showed the maximum frequency on the MOF-1s surface, so the possible interactions of MOF-1s with fibrinogen also studied using fluorescence spectroscopy and corresponding data were plotted. According to the obtained data from MTT assay, these structures have concentration-dependent toxicity. In brief, based on the obtained data in the current study, the designed MOF can be introduced as a new desirable carrier for drug/gen delivery after further prerequisite assessments.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-020-71170-z</identifier><identifier>PMID: 32884004</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>639/301 ; 639/301/54 ; 639/301/54/1754 ; Breast Neoplasms - drug therapy ; Breast Neoplasms - pathology ; Cell culture ; Cell Proliferation ; Computer applications ; Copper ; Drug Delivery Systems ; Female ; Fluorescence ; Gel electrophoresis ; Genomes ; Humanities and Social Sciences ; Humans ; Infrared spectroscopy ; Irradiation ; Mathematical models ; MCF-7 Cells ; Metabolic pathways ; Metabolism ; Metal-Organic Frameworks - chemistry ; Metal-Organic Frameworks - pharmacology ; multidisciplinary ; Ordinary differential equations ; Protein Corona - chemistry ; Science ; Science (multidisciplinary) ; Serum Albumin, Human - pharmacology ; Serum Globulins - pharmacology ; Sodium lauryl sulfate ; Stochasticity ; X-ray diffraction</subject><ispartof>Scientific reports, 2020-09, Vol.10 (1), p.14569, Article 14569</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-b7cdf2761c66f0734ffb04401bf2e54a2bd9b38428dadf777ddb3fd2391112d23</citedby><cites>FETCH-LOGICAL-c474t-b7cdf2761c66f0734ffb04401bf2e54a2bd9b38428dadf777ddb3fd2391112d23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1888631189/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1888631189?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32884004$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jafari, Samira</creatorcontrib><creatorcontrib>Izadi, Zhila</creatorcontrib><creatorcontrib>Alaei, Loghman</creatorcontrib><creatorcontrib>Jaymand, Mehdi</creatorcontrib><creatorcontrib>Samadian, Hadi</creatorcontrib><creatorcontrib>Kashani, Vali ollah</creatorcontrib><creatorcontrib>Derakhshankhah, Hossein</creatorcontrib><creatorcontrib>Hayati, Payam</creatorcontrib><creatorcontrib>Noori, Foad</creatorcontrib><creatorcontrib>Mansouri, Kamran</creatorcontrib><creatorcontrib>Moakedi, Faezeh</creatorcontrib><creatorcontrib>Janczak, Jan</creatorcontrib><creatorcontrib>Soltanian Fard, Mohammad Jaafar</creatorcontrib><creatorcontrib>Fayaz bakhsh, Nozar</creatorcontrib><title>Human plasma protein corona decreases the toxicity of pillar-layer metal organic framework</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>This scenario was designed to investigate the protein corona pattern on the pillar-layer surface of a Cu-based metal–organic framework (MOF) in human plasma. The [Cu(L)(L
/
)].1.3DMA (MOF-1) {L = 4, 4
/
-bipyridine and L
/
= 5-aminoisophthalic acid}, was synthesized through the sonochemical irradiation approach as well as characterized by various techniques like scanning electron microscopy, Fourier-transform infrared spectroscopy, X-ray powder diffraction and single-crystal X-ray diffraction. The space group was determined to be an orthorhombic space group (
Pbam
) by single-crystal X-ray diffraction. Single-crystal X-ray analyses on MOF-1 showed that Cu
+2
ion was 6-coordinated. Besides, to study and clarify interactions between MOFs and biological milieu, human whole blood plasma was selected as a model. Fluorescence spectroscopy and SDS-PAGE techniques were employed to explore quantitative and qualitative in situ characterization of protein corona as well. Furthermore, cell viability in a cancerous cell lines was evaluated by MTT assay in the presence and absence of the corona. The results from SDS-PAGE illustrated that the most adsorbed quantity among plasma proteins belongs to fibrinogen (α, β and γ chains), and this protein showed the maximum frequency on the MOF-1s surface, so the possible interactions of MOF-1s with fibrinogen also studied using fluorescence spectroscopy and corresponding data were plotted. According to the obtained data from MTT assay, these structures have concentration-dependent toxicity. In brief, based on the obtained data in the current study, the designed MOF can be introduced as a new desirable carrier for drug/gen delivery after further prerequisite assessments.</description><subject>639/301</subject><subject>639/301/54</subject><subject>639/301/54/1754</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - pathology</subject><subject>Cell culture</subject><subject>Cell Proliferation</subject><subject>Computer applications</subject><subject>Copper</subject><subject>Drug Delivery Systems</subject><subject>Female</subject><subject>Fluorescence</subject><subject>Gel electrophoresis</subject><subject>Genomes</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Infrared spectroscopy</subject><subject>Irradiation</subject><subject>Mathematical models</subject><subject>MCF-7 Cells</subject><subject>Metabolic pathways</subject><subject>Metabolism</subject><subject>Metal-Organic Frameworks - chemistry</subject><subject>Metal-Organic Frameworks - pharmacology</subject><subject>multidisciplinary</subject><subject>Ordinary differential equations</subject><subject>Protein Corona - chemistry</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Serum Albumin, Human - pharmacology</subject><subject>Serum Globulins - pharmacology</subject><subject>Sodium lauryl sulfate</subject><subject>Stochasticity</subject><subject>X-ray 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organic framework</title><author>Jafari, Samira ; Izadi, Zhila ; Alaei, Loghman ; Jaymand, Mehdi ; Samadian, Hadi ; Kashani, Vali ollah ; Derakhshankhah, Hossein ; Hayati, Payam ; Noori, Foad ; Mansouri, Kamran ; Moakedi, Faezeh ; Janczak, Jan ; Soltanian Fard, Mohammad Jaafar ; Fayaz bakhsh, Nozar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-b7cdf2761c66f0734ffb04401bf2e54a2bd9b38428dadf777ddb3fd2391112d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>639/301</topic><topic>639/301/54</topic><topic>639/301/54/1754</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - pathology</topic><topic>Cell culture</topic><topic>Cell Proliferation</topic><topic>Computer applications</topic><topic>Copper</topic><topic>Drug Delivery Systems</topic><topic>Female</topic><topic>Fluorescence</topic><topic>Gel electrophoresis</topic><topic>Genomes</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Infrared spectroscopy</topic><topic>Irradiation</topic><topic>Mathematical models</topic><topic>MCF-7 Cells</topic><topic>Metabolic pathways</topic><topic>Metabolism</topic><topic>Metal-Organic Frameworks - chemistry</topic><topic>Metal-Organic Frameworks - pharmacology</topic><topic>multidisciplinary</topic><topic>Ordinary differential equations</topic><topic>Protein Corona - chemistry</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Serum Albumin, Human - pharmacology</topic><topic>Serum Globulins - pharmacology</topic><topic>Sodium lauryl sulfate</topic><topic>Stochasticity</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jafari, Samira</creatorcontrib><creatorcontrib>Izadi, Zhila</creatorcontrib><creatorcontrib>Alaei, 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Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jafari, Samira</au><au>Izadi, Zhila</au><au>Alaei, Loghman</au><au>Jaymand, Mehdi</au><au>Samadian, Hadi</au><au>Kashani, Vali ollah</au><au>Derakhshankhah, Hossein</au><au>Hayati, Payam</au><au>Noori, Foad</au><au>Mansouri, Kamran</au><au>Moakedi, Faezeh</au><au>Janczak, Jan</au><au>Soltanian Fard, Mohammad Jaafar</au><au>Fayaz bakhsh, Nozar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human plasma protein corona decreases the toxicity of pillar-layer metal organic framework</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2020-09-03</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>14569</spage><pages>14569-</pages><artnum>14569</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>This scenario was designed to investigate the protein corona pattern on the pillar-layer surface of a Cu-based metal–organic framework (MOF) in human plasma. The [Cu(L)(L
/
)].1.3DMA (MOF-1) {L = 4, 4
/
-bipyridine and L
/
= 5-aminoisophthalic acid}, was synthesized through the sonochemical irradiation approach as well as characterized by various techniques like scanning electron microscopy, Fourier-transform infrared spectroscopy, X-ray powder diffraction and single-crystal X-ray diffraction. The space group was determined to be an orthorhombic space group (
Pbam
) by single-crystal X-ray diffraction. Single-crystal X-ray analyses on MOF-1 showed that Cu
+2
ion was 6-coordinated. Besides, to study and clarify interactions between MOFs and biological milieu, human whole blood plasma was selected as a model. Fluorescence spectroscopy and SDS-PAGE techniques were employed to explore quantitative and qualitative in situ characterization of protein corona as well. Furthermore, cell viability in a cancerous cell lines was evaluated by MTT assay in the presence and absence of the corona. The results from SDS-PAGE illustrated that the most adsorbed quantity among plasma proteins belongs to fibrinogen (α, β and γ chains), and this protein showed the maximum frequency on the MOF-1s surface, so the possible interactions of MOF-1s with fibrinogen also studied using fluorescence spectroscopy and corresponding data were plotted. According to the obtained data from MTT assay, these structures have concentration-dependent toxicity. In brief, based on the obtained data in the current study, the designed MOF can be introduced as a new desirable carrier for drug/gen delivery after further prerequisite assessments.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32884004</pmid><doi>10.1038/s41598-020-71170-z</doi><oa>free_for_read</oa></addata></record> |
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subjects | 639/301 639/301/54 639/301/54/1754 Breast Neoplasms - drug therapy Breast Neoplasms - pathology Cell culture Cell Proliferation Computer applications Copper Drug Delivery Systems Female Fluorescence Gel electrophoresis Genomes Humanities and Social Sciences Humans Infrared spectroscopy Irradiation Mathematical models MCF-7 Cells Metabolic pathways Metabolism Metal-Organic Frameworks - chemistry Metal-Organic Frameworks - pharmacology multidisciplinary Ordinary differential equations Protein Corona - chemistry Science Science (multidisciplinary) Serum Albumin, Human - pharmacology Serum Globulins - pharmacology Sodium lauryl sulfate Stochasticity X-ray diffraction |
title | Human plasma protein corona decreases the toxicity of pillar-layer metal organic framework |
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