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PHMB modified photothermally triggered nitric oxide release nanoplatform for precise synergistic therapy of wound bacterial infections
Cationic antimicrobial polymer modified NIR-controllable nitric oxide generation nanoplatform (PB-NO@PDA-PHMB) for precise synergistic therapy of wound bacterial infections. [Display omitted] Bacterial infection has been considered as a significant obstacle for wound healing. Nitric oxide (NO), as a...
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Published in: | International journal of pharmaceutics 2023-06, Vol.640, p.123014-123014, Article 123014 |
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creator | Qi, Chenyang Chen, Jie Zhuang, Ying Zhang, Yipin Zhang, Qinqin Tu, Jing |
description | Cationic antimicrobial polymer modified NIR-controllable nitric oxide generation nanoplatform (PB-NO@PDA-PHMB) for precise synergistic therapy of wound bacterial infections.
[Display omitted]
Bacterial infection has been considered as a significant obstacle for wound healing. Nitric oxide (NO), as a novel alternative for antibiotics, has emerged as a promising antibacterial agent. However, the precise spatiotemporal controlled release of NO still remains a major challenge. Herein, a near-infrared (NIR) light triggered NO release nanoplatform (designated as PB-NO@PDA-PHMB) with enhanced broad-spectrum antibacterial and anti-biofilm properties was constructed. Given that PB-NO@PDA-PHMB has strong absorption in the NIR region and exhibits excellent photothermal effect, it can rapidly trigger NO release by NIR irradiation. PB-NO@PDA-PHMB can effectively contact and capture bacteria, and then exhibit synergistic effect of photothermal and gas therapy. In vitro and in vivo experiments indicated that PB-NO@PDA-PHMB exhibited excellent biocompatibility, satisfactory synergistic antibacterial efficacy and the capability of accelerating wound healing. Under NIR irradiation (808 nm, 1 W cm−2, 7 min), PB-NO@PDA-PHMB (80 μg mL−1) achieved 100% bactericidal activity against both Gram-negative bacteria Escherichia coli (E. coli) and Gram-positive bacteria Staphyloccocus aureus (S. aureus), removed 58.94% of S. aureus biofilm. Therefore, this all-in-one antibacterial nanoplatform with high NIR responsiveness provides a promising antibiotic-free strategy for bacterial infection treatment. |
doi_str_mv | 10.1016/j.ijpharm.2023.123014 |
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[Display omitted]
Bacterial infection has been considered as a significant obstacle for wound healing. Nitric oxide (NO), as a novel alternative for antibiotics, has emerged as a promising antibacterial agent. However, the precise spatiotemporal controlled release of NO still remains a major challenge. Herein, a near-infrared (NIR) light triggered NO release nanoplatform (designated as PB-NO@PDA-PHMB) with enhanced broad-spectrum antibacterial and anti-biofilm properties was constructed. Given that PB-NO@PDA-PHMB has strong absorption in the NIR region and exhibits excellent photothermal effect, it can rapidly trigger NO release by NIR irradiation. PB-NO@PDA-PHMB can effectively contact and capture bacteria, and then exhibit synergistic effect of photothermal and gas therapy. In vitro and in vivo experiments indicated that PB-NO@PDA-PHMB exhibited excellent biocompatibility, satisfactory synergistic antibacterial efficacy and the capability of accelerating wound healing. Under NIR irradiation (808 nm, 1 W cm−2, 7 min), PB-NO@PDA-PHMB (80 μg mL−1) achieved 100% bactericidal activity against both Gram-negative bacteria Escherichia coli (E. coli) and Gram-positive bacteria Staphyloccocus aureus (S. aureus), removed 58.94% of S. aureus biofilm. Therefore, this all-in-one antibacterial nanoplatform with high NIR responsiveness provides a promising antibiotic-free strategy for bacterial infection treatment.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2023.123014</identifier><identifier>PMID: 37146954</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Anti-Bacterial Agents - pharmacology ; Antibacterial ; Bacterial Infections ; Escherichia coli ; Humans ; Nitric Oxide ; Nitric oxide release ; Photothermal therapy ; Prussian blue ; Staphylococcus aureus ; Synergistic therapy</subject><ispartof>International journal of pharmaceutics, 2023-06, Vol.640, p.123014-123014, Article 123014</ispartof><rights>2023 Elsevier B.V.</rights><rights>Copyright © 2023 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-d66708ce0d40c811fdd7e9386bbf82c56e5a3843afc57f4b1d97c6c07d54b9f43</citedby><cites>FETCH-LOGICAL-c365t-d66708ce0d40c811fdd7e9386bbf82c56e5a3843afc57f4b1d97c6c07d54b9f43</cites><orcidid>0000-0002-5616-8350</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/37146954$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qi, Chenyang</creatorcontrib><creatorcontrib>Chen, Jie</creatorcontrib><creatorcontrib>Zhuang, Ying</creatorcontrib><creatorcontrib>Zhang, Yipin</creatorcontrib><creatorcontrib>Zhang, Qinqin</creatorcontrib><creatorcontrib>Tu, Jing</creatorcontrib><title>PHMB modified photothermally triggered nitric oxide release nanoplatform for precise synergistic therapy of wound bacterial infections</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>Cationic antimicrobial polymer modified NIR-controllable nitric oxide generation nanoplatform (PB-NO@PDA-PHMB) for precise synergistic therapy of wound bacterial infections.
[Display omitted]
Bacterial infection has been considered as a significant obstacle for wound healing. Nitric oxide (NO), as a novel alternative for antibiotics, has emerged as a promising antibacterial agent. However, the precise spatiotemporal controlled release of NO still remains a major challenge. Herein, a near-infrared (NIR) light triggered NO release nanoplatform (designated as PB-NO@PDA-PHMB) with enhanced broad-spectrum antibacterial and anti-biofilm properties was constructed. Given that PB-NO@PDA-PHMB has strong absorption in the NIR region and exhibits excellent photothermal effect, it can rapidly trigger NO release by NIR irradiation. PB-NO@PDA-PHMB can effectively contact and capture bacteria, and then exhibit synergistic effect of photothermal and gas therapy. In vitro and in vivo experiments indicated that PB-NO@PDA-PHMB exhibited excellent biocompatibility, satisfactory synergistic antibacterial efficacy and the capability of accelerating wound healing. Under NIR irradiation (808 nm, 1 W cm−2, 7 min), PB-NO@PDA-PHMB (80 μg mL−1) achieved 100% bactericidal activity against both Gram-negative bacteria Escherichia coli (E. coli) and Gram-positive bacteria Staphyloccocus aureus (S. aureus), removed 58.94% of S. aureus biofilm. Therefore, this all-in-one antibacterial nanoplatform with high NIR responsiveness provides a promising antibiotic-free strategy for bacterial infection treatment.</description><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibacterial</subject><subject>Bacterial Infections</subject><subject>Escherichia coli</subject><subject>Humans</subject><subject>Nitric Oxide</subject><subject>Nitric oxide release</subject><subject>Photothermal therapy</subject><subject>Prussian blue</subject><subject>Staphylococcus aureus</subject><subject>Synergistic therapy</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFUcFuEzEQtRCIpoVPAPnIZYO99tq7JwQV0EpF7aGcLa89Thzt2ovtAPmBfjeOErhymRlp3puneQ-hN5SsKaHi_W7td8tWp3ndkpatacsI5c_QivaSNYxL8RytCJN901HJLtBlzjtCiGgpe4kumKRcDB1foaeHm2-f8Bytdx4sXraxxLKFNOtpOuCS_GYDqS6Cr7PB8be3gBNMoDPgoENcJl1cTDOuBS8JjK-LfAiQNj6XSjle08sBR4d_xX2weNSmQPJ6wj44MMXHkF-hF05PGV6f-xX6_uXz4_VNc3f_9fb6411jmOhKY4WQpDdALCemp9RZK2FgvRhH17emE9Bp1nOmnemk4yO1gzTCEGk7Pg6Osyv07nR3SfHHHnJRs88GpkkHiPus2p6SoXrD2grtTlCTYs4JnFqSn3U6KErUMQK1U-cI1DECdYqg8t6eJfbjDPYf66_nFfDhBID66E8PSWXjIRiwvtpXlI3-PxJ_ABZLnic</recordid><startdate>20230610</startdate><enddate>20230610</enddate><creator>Qi, Chenyang</creator><creator>Chen, Jie</creator><creator>Zhuang, Ying</creator><creator>Zhang, Yipin</creator><creator>Zhang, Qinqin</creator><creator>Tu, Jing</creator><general>Elsevier B.V</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/0000-0002-5616-8350</orcidid></search><sort><creationdate>20230610</creationdate><title>PHMB modified photothermally triggered nitric oxide release nanoplatform for precise synergistic therapy of wound bacterial infections</title><author>Qi, Chenyang ; Chen, Jie ; Zhuang, Ying ; Zhang, Yipin ; Zhang, Qinqin ; Tu, Jing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-d66708ce0d40c811fdd7e9386bbf82c56e5a3843afc57f4b1d97c6c07d54b9f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antibacterial</topic><topic>Bacterial Infections</topic><topic>Escherichia coli</topic><topic>Humans</topic><topic>Nitric Oxide</topic><topic>Nitric oxide release</topic><topic>Photothermal therapy</topic><topic>Prussian blue</topic><topic>Staphylococcus aureus</topic><topic>Synergistic therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qi, Chenyang</creatorcontrib><creatorcontrib>Chen, Jie</creatorcontrib><creatorcontrib>Zhuang, Ying</creatorcontrib><creatorcontrib>Zhang, Yipin</creatorcontrib><creatorcontrib>Zhang, Qinqin</creatorcontrib><creatorcontrib>Tu, Jing</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>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qi, Chenyang</au><au>Chen, Jie</au><au>Zhuang, Ying</au><au>Zhang, Yipin</au><au>Zhang, Qinqin</au><au>Tu, Jing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PHMB modified photothermally triggered nitric oxide release nanoplatform for precise synergistic therapy of wound bacterial infections</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2023-06-10</date><risdate>2023</risdate><volume>640</volume><spage>123014</spage><epage>123014</epage><pages>123014-123014</pages><artnum>123014</artnum><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>Cationic antimicrobial polymer modified NIR-controllable nitric oxide generation nanoplatform (PB-NO@PDA-PHMB) for precise synergistic therapy of wound bacterial infections.
[Display omitted]
Bacterial infection has been considered as a significant obstacle for wound healing. Nitric oxide (NO), as a novel alternative for antibiotics, has emerged as a promising antibacterial agent. However, the precise spatiotemporal controlled release of NO still remains a major challenge. Herein, a near-infrared (NIR) light triggered NO release nanoplatform (designated as PB-NO@PDA-PHMB) with enhanced broad-spectrum antibacterial and anti-biofilm properties was constructed. Given that PB-NO@PDA-PHMB has strong absorption in the NIR region and exhibits excellent photothermal effect, it can rapidly trigger NO release by NIR irradiation. PB-NO@PDA-PHMB can effectively contact and capture bacteria, and then exhibit synergistic effect of photothermal and gas therapy. In vitro and in vivo experiments indicated that PB-NO@PDA-PHMB exhibited excellent biocompatibility, satisfactory synergistic antibacterial efficacy and the capability of accelerating wound healing. Under NIR irradiation (808 nm, 1 W cm−2, 7 min), PB-NO@PDA-PHMB (80 μg mL−1) achieved 100% bactericidal activity against both Gram-negative bacteria Escherichia coli (E. coli) and Gram-positive bacteria Staphyloccocus aureus (S. aureus), removed 58.94% of S. aureus biofilm. Therefore, this all-in-one antibacterial nanoplatform with high NIR responsiveness provides a promising antibiotic-free strategy for bacterial infection treatment.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>37146954</pmid><doi>10.1016/j.ijpharm.2023.123014</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-5616-8350</orcidid></addata></record> |
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subjects | Anti-Bacterial Agents - pharmacology Antibacterial Bacterial Infections Escherichia coli Humans Nitric Oxide Nitric oxide release Photothermal therapy Prussian blue Staphylococcus aureus Synergistic therapy |
title | PHMB modified photothermally triggered nitric oxide release nanoplatform for precise synergistic therapy of wound bacterial infections |
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