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Application of a Novel “Turn-on” Fluorescent Material to the Detection of Aluminum Ion in Blood Serum
A novel “turn-on” fluorescent bioprobe, 1,2,3,4,5-penta(4-carboxyphenyl)pyrrole sodium salt (PPPNa), with aggregation-enhanced emission characteristics was synthesized for the in situ quantitative detection of Al3+ in serum. It exhibited a high selectivity to Al3+ in both simulated serum and fetal...
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Published in: | ACS applied materials & interfaces 2018-07, Vol.10 (28), p.23667-23673 |
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description | A novel “turn-on” fluorescent bioprobe, 1,2,3,4,5-penta(4-carboxyphenyl)pyrrole sodium salt (PPPNa), with aggregation-enhanced emission characteristics was synthesized for the in situ quantitative detection of Al3+ in serum. It exhibited a high selectivity to Al3+ in both simulated serum and fetal calf serum with no interferences from other metal ions or serum components observed and no isolation required. A weak interaction between PPPNa and serum albumin was found, which caused no interference, but enhanced fluorescence response of PPPNa to Al3+ and improved detection sensitivity. The limit of detection was determined to be 1.50 μmol/L Al3+ in phosphate-buffered saline solution containing 33 μg/mL bovine serum albumin (BSA) and decreased to 0.98 μmol/L as BSA concentration increased to 100 μg/mL. The fluorescence “turn-on” mechanism of the PPPNa probe to detect Al3+ was proposed. A bidentate complex is formed between the carboxy group of PPPNa and Al3+, causing the photoluminescence (PL) emission enhancement by aggregation. BSA chains further strengthen the stacking compactness of the aggregates of PPPNa and Al3+ and consequently enhance the PL emission of PPPNa by further promoting the restriction of intramolecular rotation of the phenyl ring. Its application to the in situ Al3+ was successfully demonstrated with HeLa cells and NIH 3T3 cells. The low cytotoxicity and highly selective response of PPPNa to Al3+ endow its great potentials to in vivo detecting and imaging of Al3+ as well as an absorbent of Al3+. |
doi_str_mv | 10.1021/acsami.8b07658 |
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It exhibited a high selectivity to Al3+ in both simulated serum and fetal calf serum with no interferences from other metal ions or serum components observed and no isolation required. A weak interaction between PPPNa and serum albumin was found, which caused no interference, but enhanced fluorescence response of PPPNa to Al3+ and improved detection sensitivity. The limit of detection was determined to be 1.50 μmol/L Al3+ in phosphate-buffered saline solution containing 33 μg/mL bovine serum albumin (BSA) and decreased to 0.98 μmol/L as BSA concentration increased to 100 μg/mL. The fluorescence “turn-on” mechanism of the PPPNa probe to detect Al3+ was proposed. A bidentate complex is formed between the carboxy group of PPPNa and Al3+, causing the photoluminescence (PL) emission enhancement by aggregation. BSA chains further strengthen the stacking compactness of the aggregates of PPPNa and Al3+ and consequently enhance the PL emission of PPPNa by further promoting the restriction of intramolecular rotation of the phenyl ring. Its application to the in situ Al3+ was successfully demonstrated with HeLa cells and NIH 3T3 cells. The low cytotoxicity and highly selective response of PPPNa to Al3+ endow its great potentials to in vivo detecting and imaging of Al3+ as well as an absorbent of Al3+.</description><identifier>ISSN: 1944-8244</identifier><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.8b07658</identifier><identifier>PMID: 29932319</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Aluminum - blood ; Animals ; Cell Line ; Fluorescent Dyes ; Humans ; Mice ; Spectrometry, Fluorescence</subject><ispartof>ACS applied materials & interfaces, 2018-07, Vol.10 (28), p.23667-23673</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a330t-a6e26a112271cf7d9f159db2e036b0c1587799e8823ac603e2d4dd4a6588739b3</citedby><cites>FETCH-LOGICAL-a330t-a6e26a112271cf7d9f159db2e036b0c1587799e8823ac603e2d4dd4a6588739b3</cites><orcidid>0000-0002-4847-1472 ; 0000-0003-0239-9601 ; 0000-0001-7437-0678</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29932319$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Pai</creatorcontrib><creatorcontrib>Li, Wangyang</creatorcontrib><creatorcontrib>Guo, Shuai</creatorcontrib><creatorcontrib>Xu, Dongrui</creatorcontrib><creatorcontrib>Wang, Mengni</creatorcontrib><creatorcontrib>Shi, Jianbing</creatorcontrib><creatorcontrib>Cai, Zhengxu</creatorcontrib><creatorcontrib>Tong, Bin</creatorcontrib><creatorcontrib>Dong, Yuping</creatorcontrib><title>Application of a Novel “Turn-on” Fluorescent Material to the Detection of Aluminum Ion in Blood Serum</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl. Mater. Interfaces</addtitle><description>A novel “turn-on” fluorescent bioprobe, 1,2,3,4,5-penta(4-carboxyphenyl)pyrrole sodium salt (PPPNa), with aggregation-enhanced emission characteristics was synthesized for the in situ quantitative detection of Al3+ in serum. It exhibited a high selectivity to Al3+ in both simulated serum and fetal calf serum with no interferences from other metal ions or serum components observed and no isolation required. A weak interaction between PPPNa and serum albumin was found, which caused no interference, but enhanced fluorescence response of PPPNa to Al3+ and improved detection sensitivity. The limit of detection was determined to be 1.50 μmol/L Al3+ in phosphate-buffered saline solution containing 33 μg/mL bovine serum albumin (BSA) and decreased to 0.98 μmol/L as BSA concentration increased to 100 μg/mL. The fluorescence “turn-on” mechanism of the PPPNa probe to detect Al3+ was proposed. A bidentate complex is formed between the carboxy group of PPPNa and Al3+, causing the photoluminescence (PL) emission enhancement by aggregation. BSA chains further strengthen the stacking compactness of the aggregates of PPPNa and Al3+ and consequently enhance the PL emission of PPPNa by further promoting the restriction of intramolecular rotation of the phenyl ring. Its application to the in situ Al3+ was successfully demonstrated with HeLa cells and NIH 3T3 cells. The low cytotoxicity and highly selective response of PPPNa to Al3+ endow its great potentials to in vivo detecting and imaging of Al3+ as well as an absorbent of Al3+.</description><subject>Aluminum - blood</subject><subject>Animals</subject><subject>Cell Line</subject><subject>Fluorescent Dyes</subject><subject>Humans</subject><subject>Mice</subject><subject>Spectrometry, Fluorescence</subject><issn>1944-8244</issn><issn>1944-8252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kMlOwzAURS0EoqWwZYm8REgpHjLYyzIUKjEsKOvISV6EKycudoLEjg-Bn-uXYNRhx8rP0rlX7x2ETikZU8LopSq9avRYFCRLE7GHhlTGcSRYwvZ3cxwP0JH3C0JSzkhyiAZMSs44lUOkJ8ul0aXqtG2xrbHCT_YDDF59fc9710a2XX394KnprQNfQtvhR9WB08rgzuLuDfANdFBu4xPTN7rtGzwLf93iK2NthV_A9c0xOqiV8XCyeUfodXo7v76PHp7vZteTh0hxTrpIpcBSRSljGS3rrJI1TWRVMCA8LUhJE5FlUoIQjKsyJRxYFVdVrML1IuOy4CN0vu5dOvveg-_yRofNjVEt2N7nwYBICJeCBnS8RktnvXdQ50unG-U-c0ryP735Wm--0RsCZ5vuvmig2uFbnwG4WAMhmC9sMBhO_a_tFyNrhjg</recordid><startdate>20180718</startdate><enddate>20180718</enddate><creator>Liu, Pai</creator><creator>Li, Wangyang</creator><creator>Guo, Shuai</creator><creator>Xu, Dongrui</creator><creator>Wang, Mengni</creator><creator>Shi, Jianbing</creator><creator>Cai, Zhengxu</creator><creator>Tong, Bin</creator><creator>Dong, Yuping</creator><general>American Chemical Society</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/0000-0002-4847-1472</orcidid><orcidid>https://orcid.org/0000-0003-0239-9601</orcidid><orcidid>https://orcid.org/0000-0001-7437-0678</orcidid></search><sort><creationdate>20180718</creationdate><title>Application of a Novel “Turn-on” Fluorescent Material to the Detection of Aluminum Ion in Blood Serum</title><author>Liu, Pai ; Li, Wangyang ; Guo, Shuai ; Xu, Dongrui ; Wang, Mengni ; Shi, Jianbing ; Cai, Zhengxu ; Tong, Bin ; Dong, Yuping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a330t-a6e26a112271cf7d9f159db2e036b0c1587799e8823ac603e2d4dd4a6588739b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aluminum - blood</topic><topic>Animals</topic><topic>Cell Line</topic><topic>Fluorescent Dyes</topic><topic>Humans</topic><topic>Mice</topic><topic>Spectrometry, Fluorescence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Pai</creatorcontrib><creatorcontrib>Li, Wangyang</creatorcontrib><creatorcontrib>Guo, Shuai</creatorcontrib><creatorcontrib>Xu, Dongrui</creatorcontrib><creatorcontrib>Wang, Mengni</creatorcontrib><creatorcontrib>Shi, Jianbing</creatorcontrib><creatorcontrib>Cai, Zhengxu</creatorcontrib><creatorcontrib>Tong, Bin</creatorcontrib><creatorcontrib>Dong, Yuping</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>ACS applied materials & interfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Pai</au><au>Li, Wangyang</au><au>Guo, Shuai</au><au>Xu, Dongrui</au><au>Wang, Mengni</au><au>Shi, Jianbing</au><au>Cai, Zhengxu</au><au>Tong, Bin</au><au>Dong, Yuping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of a Novel “Turn-on” Fluorescent Material to the Detection of Aluminum Ion in Blood Serum</atitle><jtitle>ACS applied materials & interfaces</jtitle><addtitle>ACS Appl. Mater. Interfaces</addtitle><date>2018-07-18</date><risdate>2018</risdate><volume>10</volume><issue>28</issue><spage>23667</spage><epage>23673</epage><pages>23667-23673</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><abstract>A novel “turn-on” fluorescent bioprobe, 1,2,3,4,5-penta(4-carboxyphenyl)pyrrole sodium salt (PPPNa), with aggregation-enhanced emission characteristics was synthesized for the in situ quantitative detection of Al3+ in serum. It exhibited a high selectivity to Al3+ in both simulated serum and fetal calf serum with no interferences from other metal ions or serum components observed and no isolation required. A weak interaction between PPPNa and serum albumin was found, which caused no interference, but enhanced fluorescence response of PPPNa to Al3+ and improved detection sensitivity. The limit of detection was determined to be 1.50 μmol/L Al3+ in phosphate-buffered saline solution containing 33 μg/mL bovine serum albumin (BSA) and decreased to 0.98 μmol/L as BSA concentration increased to 100 μg/mL. The fluorescence “turn-on” mechanism of the PPPNa probe to detect Al3+ was proposed. A bidentate complex is formed between the carboxy group of PPPNa and Al3+, causing the photoluminescence (PL) emission enhancement by aggregation. BSA chains further strengthen the stacking compactness of the aggregates of PPPNa and Al3+ and consequently enhance the PL emission of PPPNa by further promoting the restriction of intramolecular rotation of the phenyl ring. Its application to the in situ Al3+ was successfully demonstrated with HeLa cells and NIH 3T3 cells. The low cytotoxicity and highly selective response of PPPNa to Al3+ endow its great potentials to in vivo detecting and imaging of Al3+ as well as an absorbent of Al3+.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>29932319</pmid><doi>10.1021/acsami.8b07658</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-4847-1472</orcidid><orcidid>https://orcid.org/0000-0003-0239-9601</orcidid><orcidid>https://orcid.org/0000-0001-7437-0678</orcidid></addata></record> |
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subjects | Aluminum - blood Animals Cell Line Fluorescent Dyes Humans Mice Spectrometry, Fluorescence |
title | Application of a Novel “Turn-on” Fluorescent Material to the Detection of Aluminum Ion in Blood Serum |
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