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Designing an “Off–On” Fluorescence Sensor Based on Cluster-Based CaII-Metal–Organic Frameworks for Detection of l‑Cysteine in Biological Fluids
Recently, luminescent metal–organic framework (MOF) materials have attracted considerable attention in fluorescence sensing. In this essay, we prepared a new cluster-based CaII-MOFs {[Ca1.5(μ8-HL1)(DMF)2]·DMF} n (1) with good water dispersibility, excellent photoluminescence properties (FL quantum...
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Published in: | Langmuir 2019-07, Vol.35 (30), p.9885-9895 |
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creator | Yang, Bin Li, Xinshu An, Jundan Zhang, Huimin Liu, Manman Cheng, Yue Ding, Bin Li, Yan |
description | Recently, luminescent metal–organic framework (MOF) materials have attracted considerable attention in fluorescence sensing. In this essay, we prepared a new cluster-based CaII-MOFs {[Ca1.5(μ8-HL1)(DMF)2]·DMF} n (1) with good water dispersibility, excellent photoluminescence properties (FL quantum yield of 20.37%) and great fluorescence stability. Further, it was employed to design as an “off–on” fluorescence sensor for sensitive detection of l-cysteine. This proposed strategy was that fluorescence of CaII-MOFs 1 was quenched for providing a low fluorescence background by the introduction of Pb2+ forming the CaII-MOFs 1/Pb2+ hybrid system. The quenching effect could be ascribed to the static quenching mechanism because of the formation of ground-state complexes and coordination interactions between the free carboxyl of H4L1 ligands of CaII-MOFs 1 and Pb2+. Then, with the addition of l-cysteine into the CaII-MOFs 1/Pb2+ hybrid system, the fluorescence signal was immediately restored. This result was because the Pb2+ was gradually released from the hybrid system by chelation interactions between the −SH groups of l-cysteine and Pb2+. This method received a relative wide linear range varying from 0.05 to 40 μM and a low detection limit of 15 nM for detection of l-cysteine. This proposed strategy was also successfully applied to detect l-cysteine in human serum samples with satisfactory recoveries from 95.9 to 101.5%. |
doi_str_mv | 10.1021/acs.langmuir.9b01479 |
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In this essay, we prepared a new cluster-based CaII-MOFs {[Ca1.5(μ8-HL1)(DMF)2]·DMF} n (1) with good water dispersibility, excellent photoluminescence properties (FL quantum yield of 20.37%) and great fluorescence stability. Further, it was employed to design as an “off–on” fluorescence sensor for sensitive detection of l-cysteine. This proposed strategy was that fluorescence of CaII-MOFs 1 was quenched for providing a low fluorescence background by the introduction of Pb2+ forming the CaII-MOFs 1/Pb2+ hybrid system. The quenching effect could be ascribed to the static quenching mechanism because of the formation of ground-state complexes and coordination interactions between the free carboxyl of H4L1 ligands of CaII-MOFs 1 and Pb2+. Then, with the addition of l-cysteine into the CaII-MOFs 1/Pb2+ hybrid system, the fluorescence signal was immediately restored. This result was because the Pb2+ was gradually released from the hybrid system by chelation interactions between the −SH groups of l-cysteine and Pb2+. This method received a relative wide linear range varying from 0.05 to 40 μM and a low detection limit of 15 nM for detection of l-cysteine. This proposed strategy was also successfully applied to detect l-cysteine in human serum samples with satisfactory recoveries from 95.9 to 101.5%.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/acs.langmuir.9b01479</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Langmuir, 2019-07, Vol.35 (30), p.9885-9895</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-2690-0520</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Yang, Bin</creatorcontrib><creatorcontrib>Li, Xinshu</creatorcontrib><creatorcontrib>An, Jundan</creatorcontrib><creatorcontrib>Zhang, Huimin</creatorcontrib><creatorcontrib>Liu, Manman</creatorcontrib><creatorcontrib>Cheng, Yue</creatorcontrib><creatorcontrib>Ding, Bin</creatorcontrib><creatorcontrib>Li, Yan</creatorcontrib><title>Designing an “Off–On” Fluorescence Sensor Based on Cluster-Based CaII-Metal–Organic Frameworks for Detection of l‑Cysteine in Biological Fluids</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>Recently, luminescent metal–organic framework (MOF) materials have attracted considerable attention in fluorescence sensing. In this essay, we prepared a new cluster-based CaII-MOFs {[Ca1.5(μ8-HL1)(DMF)2]·DMF} n (1) with good water dispersibility, excellent photoluminescence properties (FL quantum yield of 20.37%) and great fluorescence stability. Further, it was employed to design as an “off–on” fluorescence sensor for sensitive detection of l-cysteine. This proposed strategy was that fluorescence of CaII-MOFs 1 was quenched for providing a low fluorescence background by the introduction of Pb2+ forming the CaII-MOFs 1/Pb2+ hybrid system. The quenching effect could be ascribed to the static quenching mechanism because of the formation of ground-state complexes and coordination interactions between the free carboxyl of H4L1 ligands of CaII-MOFs 1 and Pb2+. Then, with the addition of l-cysteine into the CaII-MOFs 1/Pb2+ hybrid system, the fluorescence signal was immediately restored. This result was because the Pb2+ was gradually released from the hybrid system by chelation interactions between the −SH groups of l-cysteine and Pb2+. This method received a relative wide linear range varying from 0.05 to 40 μM and a low detection limit of 15 nM for detection of l-cysteine. 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In this essay, we prepared a new cluster-based CaII-MOFs {[Ca1.5(μ8-HL1)(DMF)2]·DMF} n (1) with good water dispersibility, excellent photoluminescence properties (FL quantum yield of 20.37%) and great fluorescence stability. Further, it was employed to design as an “off–on” fluorescence sensor for sensitive detection of l-cysteine. This proposed strategy was that fluorescence of CaII-MOFs 1 was quenched for providing a low fluorescence background by the introduction of Pb2+ forming the CaII-MOFs 1/Pb2+ hybrid system. The quenching effect could be ascribed to the static quenching mechanism because of the formation of ground-state complexes and coordination interactions between the free carboxyl of H4L1 ligands of CaII-MOFs 1 and Pb2+. Then, with the addition of l-cysteine into the CaII-MOFs 1/Pb2+ hybrid system, the fluorescence signal was immediately restored. This result was because the Pb2+ was gradually released from the hybrid system by chelation interactions between the −SH groups of l-cysteine and Pb2+. This method received a relative wide linear range varying from 0.05 to 40 μM and a low detection limit of 15 nM for detection of l-cysteine. This proposed strategy was also successfully applied to detect l-cysteine in human serum samples with satisfactory recoveries from 95.9 to 101.5%.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.langmuir.9b01479</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-2690-0520</orcidid></addata></record> |
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title | Designing an “Off–On” Fluorescence Sensor Based on Cluster-Based CaII-Metal–Organic Frameworks for Detection of l‑Cysteine in Biological Fluids |
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