Loading…

Dual-targeted and viscosity-sensitive infrared AIE photosensitizer based on tumor microenvironmental response for photodynamic cancer therapy

Due to their excellent capabilities in photodynamic therapy (PDT) and aggregation-induced emission, (AIE) photosensitizers have attracted a great deal of attention. However, the poor water solubilities of current AIE photosensitizers limit their widespread in vivo application and PDT productivity. A...

Full description

Saved in:
Bibliographic Details
Published in:New journal of chemistry 2024-11, Vol.48 (45), p.19136-19143
Main Authors: Wen, Xiaoye, Shi, Zhilin, Huang, Yongfei, Fan, Zhefeng
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c170t-3f5ad744be914a53c5361ae8490357f936d0f2d1ab9c1ef5cc76bd911fb8533c3
container_end_page 19143
container_issue 45
container_start_page 19136
container_title New journal of chemistry
container_volume 48
creator Wen, Xiaoye
Shi, Zhilin
Huang, Yongfei
Fan, Zhefeng
description Due to their excellent capabilities in photodynamic therapy (PDT) and aggregation-induced emission, (AIE) photosensitizers have attracted a great deal of attention. However, the poor water solubilities of current AIE photosensitizers limit their widespread in vivo application and PDT productivity. AIE photosensitizers with triphenylamine as electron-donating moiety and pyridine as electron-absorbing group can enhance the D-A effort, thus improving the intramolecular charge transfer (ICT) and extending the emission wavelength. At the same time, Δ E st was reduced and intersystem crossing processes was promoted due to the D-A effect of the photosensitizers, thus increasing the probability of ROS generation. Herein, a dual-organelle targeted and viscosity-sensitive infrared AIE photosensitizer (NES-OH) with a D-A structure was developed and synthesized. The NES-OH had good water solubility and good linear relationship with concentration. The NES-OH exhibited bright fluorescence at 620 nm with a quantum yield of 66.75% and had high 1 O 2 generation efficiency, as well as good biocompatibility and photostability. The NES-OH can target mitochondria and lysosomes and also monitor lysosomes and mitochondrial viscosity changes in real time or in situ in living cells. More interestingly, in the acidic environment of cancer cells, the structure of the NES-OH changed with the appearance of specific morpholine groups, leading to the targeting of lysosomes and further distinguishing and detecting normal and cancer cells. The in vitro and in vivo study demonstrated that the NES-OH can inhibit tumor growth efficiently upon light exposure. This work constructed an effective photosensitizer for diagnosing and treating cancers and evaluating PDT efficacy. Due to their excellent capabilities in photodynamic therapy (PDT), aggregation-induced emission (AIE) photosensitizers have attracted a great deal of attention.
doi_str_mv 10.1039/d4nj03321c
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1039_D4NJ03321C</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3129485148</sourcerecordid><originalsourceid>FETCH-LOGICAL-c170t-3f5ad744be914a53c5361ae8490357f936d0f2d1ab9c1ef5cc76bd911fb8533c3</originalsourceid><addsrcrecordid>eNpFkU9LAzEQxYMoWKsX70LAm7Ca2WT_5FjaqpWiFz0v2Wxit3STNUkL63fwOxtb0dMMvN-8Yd4gdAnkFgjldw0za0JpCvIIjYDmPOFpDsexB8YSkrH8FJ15vyYEoMhhhL5mW7FJgnDvKqgGC9PgXeul9W0YEq9MrO1O4dZoJ1wEJos57lc22F_tUzlcCx8Va3DYdtbhrpXOKrNrnTWdMkFssFO-t8YrrKO-H28GIyKIpTAyWoSVcqIfztGJFhuvLn7rGL3dz1-nj8ny5WExnSwTCQUJCdWZaArGasWBiYzKjOYgVMk4oVmhOc0botMGRM0lKJ1JWeR1wwF0XWaUSjpG1wff3tmPrfKhWtutM3FlRSHlrMyAlZG6OVDxHu-d0lXv2k64oQJS_cRdzdjz0z7uaYSvDrDz8o_7fwf9BvDLgIc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3129485148</pqid></control><display><type>article</type><title>Dual-targeted and viscosity-sensitive infrared AIE photosensitizer based on tumor microenvironmental response for photodynamic cancer therapy</title><source>Royal Society of Chemistry</source><creator>Wen, Xiaoye ; Shi, Zhilin ; Huang, Yongfei ; Fan, Zhefeng</creator><creatorcontrib>Wen, Xiaoye ; Shi, Zhilin ; Huang, Yongfei ; Fan, Zhefeng</creatorcontrib><description>Due to their excellent capabilities in photodynamic therapy (PDT) and aggregation-induced emission, (AIE) photosensitizers have attracted a great deal of attention. However, the poor water solubilities of current AIE photosensitizers limit their widespread in vivo application and PDT productivity. AIE photosensitizers with triphenylamine as electron-donating moiety and pyridine as electron-absorbing group can enhance the D-A effort, thus improving the intramolecular charge transfer (ICT) and extending the emission wavelength. At the same time, Δ E st was reduced and intersystem crossing processes was promoted due to the D-A effect of the photosensitizers, thus increasing the probability of ROS generation. Herein, a dual-organelle targeted and viscosity-sensitive infrared AIE photosensitizer (NES-OH) with a D-A structure was developed and synthesized. The NES-OH had good water solubility and good linear relationship with concentration. The NES-OH exhibited bright fluorescence at 620 nm with a quantum yield of 66.75% and had high 1 O 2 generation efficiency, as well as good biocompatibility and photostability. The NES-OH can target mitochondria and lysosomes and also monitor lysosomes and mitochondrial viscosity changes in real time or in situ in living cells. More interestingly, in the acidic environment of cancer cells, the structure of the NES-OH changed with the appearance of specific morpholine groups, leading to the targeting of lysosomes and further distinguishing and detecting normal and cancer cells. The in vitro and in vivo study demonstrated that the NES-OH can inhibit tumor growth efficiently upon light exposure. This work constructed an effective photosensitizer for diagnosing and treating cancers and evaluating PDT efficacy. Due to their excellent capabilities in photodynamic therapy (PDT), aggregation-induced emission (AIE) photosensitizers have attracted a great deal of attention.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/d4nj03321c</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Biocompatibility ; Cancer ; Charge transfer ; Effectiveness ; Emission ; In vivo methods and tests ; Lysosomes ; Solubility ; Tumors ; Viscosity</subject><ispartof>New journal of chemistry, 2024-11, Vol.48 (45), p.19136-19143</ispartof><rights>Copyright Royal Society of Chemistry 2024</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c170t-3f5ad744be914a53c5361ae8490357f936d0f2d1ab9c1ef5cc76bd911fb8533c3</cites><orcidid>0000-0003-2260-3032</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></links><search><creatorcontrib>Wen, Xiaoye</creatorcontrib><creatorcontrib>Shi, Zhilin</creatorcontrib><creatorcontrib>Huang, Yongfei</creatorcontrib><creatorcontrib>Fan, Zhefeng</creatorcontrib><title>Dual-targeted and viscosity-sensitive infrared AIE photosensitizer based on tumor microenvironmental response for photodynamic cancer therapy</title><title>New journal of chemistry</title><description>Due to their excellent capabilities in photodynamic therapy (PDT) and aggregation-induced emission, (AIE) photosensitizers have attracted a great deal of attention. However, the poor water solubilities of current AIE photosensitizers limit their widespread in vivo application and PDT productivity. AIE photosensitizers with triphenylamine as electron-donating moiety and pyridine as electron-absorbing group can enhance the D-A effort, thus improving the intramolecular charge transfer (ICT) and extending the emission wavelength. At the same time, Δ E st was reduced and intersystem crossing processes was promoted due to the D-A effect of the photosensitizers, thus increasing the probability of ROS generation. Herein, a dual-organelle targeted and viscosity-sensitive infrared AIE photosensitizer (NES-OH) with a D-A structure was developed and synthesized. The NES-OH had good water solubility and good linear relationship with concentration. The NES-OH exhibited bright fluorescence at 620 nm with a quantum yield of 66.75% and had high 1 O 2 generation efficiency, as well as good biocompatibility and photostability. The NES-OH can target mitochondria and lysosomes and also monitor lysosomes and mitochondrial viscosity changes in real time or in situ in living cells. More interestingly, in the acidic environment of cancer cells, the structure of the NES-OH changed with the appearance of specific morpholine groups, leading to the targeting of lysosomes and further distinguishing and detecting normal and cancer cells. The in vitro and in vivo study demonstrated that the NES-OH can inhibit tumor growth efficiently upon light exposure. This work constructed an effective photosensitizer for diagnosing and treating cancers and evaluating PDT efficacy. Due to their excellent capabilities in photodynamic therapy (PDT), aggregation-induced emission (AIE) photosensitizers have attracted a great deal of attention.</description><subject>Biocompatibility</subject><subject>Cancer</subject><subject>Charge transfer</subject><subject>Effectiveness</subject><subject>Emission</subject><subject>In vivo methods and tests</subject><subject>Lysosomes</subject><subject>Solubility</subject><subject>Tumors</subject><subject>Viscosity</subject><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpFkU9LAzEQxYMoWKsX70LAm7Ca2WT_5FjaqpWiFz0v2Wxit3STNUkL63fwOxtb0dMMvN-8Yd4gdAnkFgjldw0za0JpCvIIjYDmPOFpDsexB8YSkrH8FJ15vyYEoMhhhL5mW7FJgnDvKqgGC9PgXeul9W0YEq9MrO1O4dZoJ1wEJos57lc22F_tUzlcCx8Va3DYdtbhrpXOKrNrnTWdMkFssFO-t8YrrKO-H28GIyKIpTAyWoSVcqIfztGJFhuvLn7rGL3dz1-nj8ny5WExnSwTCQUJCdWZaArGasWBiYzKjOYgVMk4oVmhOc0botMGRM0lKJ1JWeR1wwF0XWaUSjpG1wff3tmPrfKhWtutM3FlRSHlrMyAlZG6OVDxHu-d0lXv2k64oQJS_cRdzdjz0z7uaYSvDrDz8o_7fwf9BvDLgIc</recordid><startdate>20241118</startdate><enddate>20241118</enddate><creator>Wen, Xiaoye</creator><creator>Shi, Zhilin</creator><creator>Huang, Yongfei</creator><creator>Fan, Zhefeng</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>H9R</scope><scope>JG9</scope><scope>KA0</scope><orcidid>https://orcid.org/0000-0003-2260-3032</orcidid></search><sort><creationdate>20241118</creationdate><title>Dual-targeted and viscosity-sensitive infrared AIE photosensitizer based on tumor microenvironmental response for photodynamic cancer therapy</title><author>Wen, Xiaoye ; Shi, Zhilin ; Huang, Yongfei ; Fan, Zhefeng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c170t-3f5ad744be914a53c5361ae8490357f936d0f2d1ab9c1ef5cc76bd911fb8533c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Biocompatibility</topic><topic>Cancer</topic><topic>Charge transfer</topic><topic>Effectiveness</topic><topic>Emission</topic><topic>In vivo methods and tests</topic><topic>Lysosomes</topic><topic>Solubility</topic><topic>Tumors</topic><topic>Viscosity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wen, Xiaoye</creatorcontrib><creatorcontrib>Shi, Zhilin</creatorcontrib><creatorcontrib>Huang, Yongfei</creatorcontrib><creatorcontrib>Fan, Zhefeng</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Illustrata: Natural Sciences</collection><collection>Materials Research Database</collection><collection>ProQuest Illustrata: Technology Collection</collection><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wen, Xiaoye</au><au>Shi, Zhilin</au><au>Huang, Yongfei</au><au>Fan, Zhefeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dual-targeted and viscosity-sensitive infrared AIE photosensitizer based on tumor microenvironmental response for photodynamic cancer therapy</atitle><jtitle>New journal of chemistry</jtitle><date>2024-11-18</date><risdate>2024</risdate><volume>48</volume><issue>45</issue><spage>19136</spage><epage>19143</epage><pages>19136-19143</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>Due to their excellent capabilities in photodynamic therapy (PDT) and aggregation-induced emission, (AIE) photosensitizers have attracted a great deal of attention. However, the poor water solubilities of current AIE photosensitizers limit their widespread in vivo application and PDT productivity. AIE photosensitizers with triphenylamine as electron-donating moiety and pyridine as electron-absorbing group can enhance the D-A effort, thus improving the intramolecular charge transfer (ICT) and extending the emission wavelength. At the same time, Δ E st was reduced and intersystem crossing processes was promoted due to the D-A effect of the photosensitizers, thus increasing the probability of ROS generation. Herein, a dual-organelle targeted and viscosity-sensitive infrared AIE photosensitizer (NES-OH) with a D-A structure was developed and synthesized. The NES-OH had good water solubility and good linear relationship with concentration. The NES-OH exhibited bright fluorescence at 620 nm with a quantum yield of 66.75% and had high 1 O 2 generation efficiency, as well as good biocompatibility and photostability. The NES-OH can target mitochondria and lysosomes and also monitor lysosomes and mitochondrial viscosity changes in real time or in situ in living cells. More interestingly, in the acidic environment of cancer cells, the structure of the NES-OH changed with the appearance of specific morpholine groups, leading to the targeting of lysosomes and further distinguishing and detecting normal and cancer cells. The in vitro and in vivo study demonstrated that the NES-OH can inhibit tumor growth efficiently upon light exposure. This work constructed an effective photosensitizer for diagnosing and treating cancers and evaluating PDT efficacy. Due to their excellent capabilities in photodynamic therapy (PDT), aggregation-induced emission (AIE) photosensitizers have attracted a great deal of attention.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d4nj03321c</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-2260-3032</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1144-0546
ispartof New journal of chemistry, 2024-11, Vol.48 (45), p.19136-19143
issn 1144-0546
1369-9261
language eng
recordid cdi_crossref_primary_10_1039_D4NJ03321C
source Royal Society of Chemistry
subjects Biocompatibility
Cancer
Charge transfer
Effectiveness
Emission
In vivo methods and tests
Lysosomes
Solubility
Tumors
Viscosity
title Dual-targeted and viscosity-sensitive infrared AIE photosensitizer based on tumor microenvironmental response for photodynamic cancer therapy
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T05%3A58%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Dual-targeted%20and%20viscosity-sensitive%20infrared%20AIE%20photosensitizer%20based%20on%20tumor%20microenvironmental%20response%20for%20photodynamic%20cancer%20therapy&rft.jtitle=New%20journal%20of%20chemistry&rft.au=Wen,%20Xiaoye&rft.date=2024-11-18&rft.volume=48&rft.issue=45&rft.spage=19136&rft.epage=19143&rft.pages=19136-19143&rft.issn=1144-0546&rft.eissn=1369-9261&rft_id=info:doi/10.1039/d4nj03321c&rft_dat=%3Cproquest_cross%3E3129485148%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c170t-3f5ad744be914a53c5361ae8490357f936d0f2d1ab9c1ef5cc76bd911fb8533c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3129485148&rft_id=info:pmid/&rfr_iscdi=true