Chitosan-naphthalimide probes for dual channel recognition of HClO and H 2 S in cells and their application in photodynamic therapy
The combination of bio-imaging with photodynamic therapy (PDT) to accomplish theranostics is promising in cancer treatment. Three chitosan-naphthalimide probes were studied in this work. 4-(5-Bromothiophen-2-yl)-1,8-naphthalic anhydride was first synthesized, and then reacted with chitosan to obtain...
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Veröffentlicht in: | International journal of biological macromolecules 2024-11, Vol.281 (Pt 4), p.136517 |
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creator | Zhao, Bo Liu, Jun Zhu, Caiqiong Cheng, Xinjian |
description | The combination of bio-imaging with photodynamic therapy (PDT) to accomplish theranostics is promising in cancer treatment. Three chitosan-naphthalimide probes were studied in this work. 4-(5-Bromothiophen-2-yl)-1,8-naphthalic anhydride was first synthesized, and then reacted with chitosan to obtain the macromolecules (CS-N-Br). The recognition group thiomorpholine or its derivatives were introduced into CS-N-Br to obtain nano-probes (CS-N-ML, CS-N-BSZ, CS-N-FSQ) eventually. The studies revealed that CS-N-ML and CS-N-FSQ exhibit high selectivity and can specifically recognize HClO and H
S. CS-N-ML and CS-N-FSQ can perform exogenous and endogenous confocal imaging of HClO and H
S in cells also. CS-N-ML's ability to target lysosomes positions indicated it could act as a lysosome-specific probe. It was discovered that the probes generate superoxide anions (O
) via a Type I mechanism. This discovery endows the probes with high photosensitizing activity even under hypoxic conditions. There is a positive correlation between the extent of the conjugated system and the photosensitivity of the probes, indicating that an enhanced conjugation leads to increased photosensitivity. Upon light irradiation, the probes generate ROS within HeLa cells. These results suggested that these probes can achieve theranostics for diseases associated with abnormal levels of HClO and H
S. |
doi_str_mv | 10.1016/j.ijbiomac.2024.136517 |
format | Article |
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S. CS-N-ML and CS-N-FSQ can perform exogenous and endogenous confocal imaging of HClO and H
S in cells also. CS-N-ML's ability to target lysosomes positions indicated it could act as a lysosome-specific probe. It was discovered that the probes generate superoxide anions (O
) via a Type I mechanism. This discovery endows the probes with high photosensitizing activity even under hypoxic conditions. There is a positive correlation between the extent of the conjugated system and the photosensitivity of the probes, indicating that an enhanced conjugation leads to increased photosensitivity. Upon light irradiation, the probes generate ROS within HeLa cells. These results suggested that these probes can achieve theranostics for diseases associated with abnormal levels of HClO and H
S.</description><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2024.136517</identifier><identifier>PMID: 39426764</identifier><language>eng</language><publisher>Netherlands</publisher><subject>Chitosan - chemistry ; Fluorescent Dyes - chemistry ; HeLa Cells ; Humans ; Hydrogen Sulfide - analysis ; Hydrogen Sulfide - chemistry ; Hypochlorous Acid ; Lysosomes - metabolism ; Naphthalimides - chemistry ; Naphthalimides - pharmacology ; Photochemotherapy - methods ; Photosensitizing Agents - chemical synthesis ; Photosensitizing Agents - chemistry ; Photosensitizing Agents - pharmacology</subject><ispartof>International journal of biological macromolecules, 2024-11, Vol.281 (Pt 4), p.136517</ispartof><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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/39426764$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhao, Bo</creatorcontrib><creatorcontrib>Liu, Jun</creatorcontrib><creatorcontrib>Zhu, Caiqiong</creatorcontrib><creatorcontrib>Cheng, Xinjian</creatorcontrib><title>Chitosan-naphthalimide probes for dual channel recognition of HClO and H 2 S in cells and their application in photodynamic therapy</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>The combination of bio-imaging with photodynamic therapy (PDT) to accomplish theranostics is promising in cancer treatment. Three chitosan-naphthalimide probes were studied in this work. 4-(5-Bromothiophen-2-yl)-1,8-naphthalic anhydride was first synthesized, and then reacted with chitosan to obtain the macromolecules (CS-N-Br). The recognition group thiomorpholine or its derivatives were introduced into CS-N-Br to obtain nano-probes (CS-N-ML, CS-N-BSZ, CS-N-FSQ) eventually. The studies revealed that CS-N-ML and CS-N-FSQ exhibit high selectivity and can specifically recognize HClO and H
S. CS-N-ML and CS-N-FSQ can perform exogenous and endogenous confocal imaging of HClO and H
S in cells also. CS-N-ML's ability to target lysosomes positions indicated it could act as a lysosome-specific probe. It was discovered that the probes generate superoxide anions (O
) via a Type I mechanism. This discovery endows the probes with high photosensitizing activity even under hypoxic conditions. There is a positive correlation between the extent of the conjugated system and the photosensitivity of the probes, indicating that an enhanced conjugation leads to increased photosensitivity. Upon light irradiation, the probes generate ROS within HeLa cells. These results suggested that these probes can achieve theranostics for diseases associated with abnormal levels of HClO and H
S.</description><subject>Chitosan - chemistry</subject><subject>Fluorescent Dyes - chemistry</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Hydrogen Sulfide - analysis</subject><subject>Hydrogen Sulfide - chemistry</subject><subject>Hypochlorous Acid</subject><subject>Lysosomes - metabolism</subject><subject>Naphthalimides - chemistry</subject><subject>Naphthalimides - pharmacology</subject><subject>Photochemotherapy - methods</subject><subject>Photosensitizing Agents - chemical synthesis</subject><subject>Photosensitizing Agents - chemistry</subject><subject>Photosensitizing Agents - pharmacology</subject><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFjs1ugzAQhK1KVZL-vEK0LwC1gUJyRq249dDco8U28SJjWzY5cO6Ll0btuacZzTcjDWN7wXPBRf0y5jT25CeUecGLKhdl_SqaO7YTh-aYcc7LLXtIaVzdCg4bti2PVVE3dbVjX62h2Sd0mcNgZoOWJlIaQvS9TjD4COqKFqRB57SFqKW_OJrJO_ADdK39AHQKOijgE8iB1NamWzQbTREwBEsSb4MVB-NnrxaHE8mfRsSwPLH7AW3Sz7_6yPbvb6e2y8K1n7Q6h0gTxuX897r8t_AN3bJWfg</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>Zhao, Bo</creator><creator>Liu, Jun</creator><creator>Zhu, Caiqiong</creator><creator>Cheng, Xinjian</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>202411</creationdate><title>Chitosan-naphthalimide probes for dual channel recognition of HClO and H 2 S in cells and their application in photodynamic therapy</title><author>Zhao, Bo ; Liu, Jun ; Zhu, Caiqiong ; Cheng, Xinjian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_394267643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Chitosan - chemistry</topic><topic>Fluorescent Dyes - chemistry</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Hydrogen Sulfide - analysis</topic><topic>Hydrogen Sulfide - chemistry</topic><topic>Hypochlorous Acid</topic><topic>Lysosomes - metabolism</topic><topic>Naphthalimides - chemistry</topic><topic>Naphthalimides - pharmacology</topic><topic>Photochemotherapy - methods</topic><topic>Photosensitizing Agents - chemical synthesis</topic><topic>Photosensitizing Agents - chemistry</topic><topic>Photosensitizing Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Bo</creatorcontrib><creatorcontrib>Liu, Jun</creatorcontrib><creatorcontrib>Zhu, Caiqiong</creatorcontrib><creatorcontrib>Cheng, Xinjian</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Bo</au><au>Liu, Jun</au><au>Zhu, Caiqiong</au><au>Cheng, Xinjian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chitosan-naphthalimide probes for dual channel recognition of HClO and H 2 S in cells and their application in photodynamic therapy</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2024-11</date><risdate>2024</risdate><volume>281</volume><issue>Pt 4</issue><spage>136517</spage><pages>136517-</pages><eissn>1879-0003</eissn><abstract>The combination of bio-imaging with photodynamic therapy (PDT) to accomplish theranostics is promising in cancer treatment. Three chitosan-naphthalimide probes were studied in this work. 4-(5-Bromothiophen-2-yl)-1,8-naphthalic anhydride was first synthesized, and then reacted with chitosan to obtain the macromolecules (CS-N-Br). The recognition group thiomorpholine or its derivatives were introduced into CS-N-Br to obtain nano-probes (CS-N-ML, CS-N-BSZ, CS-N-FSQ) eventually. The studies revealed that CS-N-ML and CS-N-FSQ exhibit high selectivity and can specifically recognize HClO and H
S. CS-N-ML and CS-N-FSQ can perform exogenous and endogenous confocal imaging of HClO and H
S in cells also. CS-N-ML's ability to target lysosomes positions indicated it could act as a lysosome-specific probe. It was discovered that the probes generate superoxide anions (O
) via a Type I mechanism. This discovery endows the probes with high photosensitizing activity even under hypoxic conditions. There is a positive correlation between the extent of the conjugated system and the photosensitivity of the probes, indicating that an enhanced conjugation leads to increased photosensitivity. Upon light irradiation, the probes generate ROS within HeLa cells. These results suggested that these probes can achieve theranostics for diseases associated with abnormal levels of HClO and H
S.</abstract><cop>Netherlands</cop><pmid>39426764</pmid><doi>10.1016/j.ijbiomac.2024.136517</doi></addata></record> |
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subjects | Chitosan - chemistry Fluorescent Dyes - chemistry HeLa Cells Humans Hydrogen Sulfide - analysis Hydrogen Sulfide - chemistry Hypochlorous Acid Lysosomes - metabolism Naphthalimides - chemistry Naphthalimides - pharmacology Photochemotherapy - methods Photosensitizing Agents - chemical synthesis Photosensitizing Agents - chemistry Photosensitizing Agents - pharmacology |
title | Chitosan-naphthalimide probes for dual channel recognition of HClO and H 2 S in cells and their application in photodynamic therapy |
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