Imaging and Targeted Antibacterial Therapy Using Chimeric Antimicrobial Peptide Micelles
Infectious diseases induced by multidrug-resistant bacteria are a challenging problem in medicine because of global rise in the drug resistance to pathogenic bacteria. Despite great efforts on the development of antibiotics and antimicrobial agents, there is still a great need to develop a strategy...
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Veröffentlicht in: | ACS applied materials & interfaces 2020-12, Vol.12 (49), p.54306-54315 |
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description | Infectious diseases induced by multidrug-resistant bacteria are a challenging problem in medicine because of global rise in the drug resistance to pathogenic bacteria. Despite great efforts on the development of antibiotics and antimicrobial agents, there is still a great need to develop a strategy to early detect bacterial infections and eradicate bacteria effectively and simultaneously. The innate immune systems of various organisms produce antimicrobial peptides, which kill a broad range of bacteria with minimal cytotoxicity to mammalian cells. Therefore, antimicrobial peptides have recently attracted increasing attention as an alternative to conventional antibiotics in antibacterial medications. Here, we report a new family of antibacterial agents, which is formulated from self-assembly of a chimeric antimicrobial lipopeptide (DSPE-HnMc) and amphiphilic biodegradable polymers. HnMc micelles could effectively bind the bacterial membrane to kill a wide spectrum of bacteria and bacterial biofilms. In the studies of mouse models of drug-resistant bacterial infections, HnMc micelles could target bacterial infections with high specificity and also kill drug-resistant bacteria effectively, demonstrating the great potential of HnMc micelles as imaging and targeted antibacterial agents. These findings also provide new insight into the design of antimicrobial peptide-based nanomedicine for detection and treatment of bacterial infections. |
doi_str_mv | 10.1021/acsami.0c13083 |
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Despite great efforts on the development of antibiotics and antimicrobial agents, there is still a great need to develop a strategy to early detect bacterial infections and eradicate bacteria effectively and simultaneously. The innate immune systems of various organisms produce antimicrobial peptides, which kill a broad range of bacteria with minimal cytotoxicity to mammalian cells. Therefore, antimicrobial peptides have recently attracted increasing attention as an alternative to conventional antibiotics in antibacterial medications. Here, we report a new family of antibacterial agents, which is formulated from self-assembly of a chimeric antimicrobial lipopeptide (DSPE-HnMc) and amphiphilic biodegradable polymers. HnMc micelles could effectively bind the bacterial membrane to kill a wide spectrum of bacteria and bacterial biofilms. In the studies of mouse models of drug-resistant bacterial infections, HnMc micelles could target bacterial infections with high specificity and also kill drug-resistant bacteria effectively, demonstrating the great potential of HnMc micelles as imaging and targeted antibacterial agents. These findings also provide new insight into the design of antimicrobial peptide-based nanomedicine for detection and treatment of bacterial infections.</description><identifier>ISSN: 1944-8244</identifier><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.0c13083</identifier><identifier>PMID: 33236874</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Antimicrobial Cationic Peptides - chemistry ; Antimicrobial Cationic Peptides - pharmacology ; Antimicrobial Cationic Peptides - therapeutic use ; Biocompatible Materials - chemistry ; Biocompatible Materials - pharmacology ; Biocompatible Materials - therapeutic use ; Biofilms - drug effects ; Biological and Medical Applications of Materials and Interfaces ; Disease Models, Animal ; Drug Design ; Drug Resistance, Bacterial - drug effects ; Female ; Gram-Negative Bacteria - drug effects ; Gram-Negative Bacteria - physiology ; Gram-Positive Bacteria - drug effects ; Gram-Positive Bacteria - physiology ; Hemolysis - drug effects ; Lung Diseases - drug therapy ; Lung Diseases - microbiology ; Lung Diseases - pathology ; Mice ; Mice, Inbred BALB C ; Micelles ; Rats ; Soft Tissue Injuries - drug therapy ; Soft Tissue Injuries - microbiology ; Soft Tissue Injuries - pathology</subject><ispartof>ACS applied materials & interfaces, 2020-12, Vol.12 (49), p.54306-54315</ispartof><rights>2020 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a330t-51de13fff8f8137b5366865024cf85c38730960899a10631dc467a2e71d73f753</citedby><cites>FETCH-LOGICAL-a330t-51de13fff8f8137b5366865024cf85c38730960899a10631dc467a2e71d73f753</cites><orcidid>0000-0003-3972-7197 ; 0000-0002-2833-3216 ; 0000-0001-9051-0183 ; 0000-0002-3816-5332 ; 0000-0003-3035-6342</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acsami.0c13083$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acsami.0c13083$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33236874$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Seong-Cheol</creatorcontrib><creatorcontrib>Ko, Changgon</creatorcontrib><creatorcontrib>Hyeon, Hyejin</creatorcontrib><creatorcontrib>Jang, Mi-Kyeong</creatorcontrib><creatorcontrib>Lee, Dongwon</creatorcontrib><title>Imaging and Targeted Antibacterial Therapy Using Chimeric Antimicrobial Peptide Micelles</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl. Mater. Interfaces</addtitle><description>Infectious diseases induced by multidrug-resistant bacteria are a challenging problem in medicine because of global rise in the drug resistance to pathogenic bacteria. Despite great efforts on the development of antibiotics and antimicrobial agents, there is still a great need to develop a strategy to early detect bacterial infections and eradicate bacteria effectively and simultaneously. The innate immune systems of various organisms produce antimicrobial peptides, which kill a broad range of bacteria with minimal cytotoxicity to mammalian cells. Therefore, antimicrobial peptides have recently attracted increasing attention as an alternative to conventional antibiotics in antibacterial medications. Here, we report a new family of antibacterial agents, which is formulated from self-assembly of a chimeric antimicrobial lipopeptide (DSPE-HnMc) and amphiphilic biodegradable polymers. HnMc micelles could effectively bind the bacterial membrane to kill a wide spectrum of bacteria and bacterial biofilms. In the studies of mouse models of drug-resistant bacterial infections, HnMc micelles could target bacterial infections with high specificity and also kill drug-resistant bacteria effectively, demonstrating the great potential of HnMc micelles as imaging and targeted antibacterial agents. These findings also provide new insight into the design of antimicrobial peptide-based nanomedicine for detection and treatment of bacterial infections.</description><subject>Animals</subject><subject>Antimicrobial Cationic Peptides - chemistry</subject><subject>Antimicrobial Cationic Peptides - pharmacology</subject><subject>Antimicrobial Cationic Peptides - therapeutic use</subject><subject>Biocompatible Materials - chemistry</subject><subject>Biocompatible Materials - pharmacology</subject><subject>Biocompatible Materials - therapeutic use</subject><subject>Biofilms - drug effects</subject><subject>Biological and Medical Applications of Materials and Interfaces</subject><subject>Disease Models, Animal</subject><subject>Drug Design</subject><subject>Drug Resistance, Bacterial - drug effects</subject><subject>Female</subject><subject>Gram-Negative Bacteria - drug effects</subject><subject>Gram-Negative Bacteria - physiology</subject><subject>Gram-Positive Bacteria - drug effects</subject><subject>Gram-Positive Bacteria - physiology</subject><subject>Hemolysis - drug effects</subject><subject>Lung Diseases - drug therapy</subject><subject>Lung Diseases - microbiology</subject><subject>Lung Diseases - pathology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Micelles</subject><subject>Rats</subject><subject>Soft Tissue Injuries - drug therapy</subject><subject>Soft Tissue Injuries - microbiology</subject><subject>Soft Tissue Injuries - pathology</subject><issn>1944-8244</issn><issn>1944-8252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kDtPwzAUhS0EolBYGVFGhJTiVxxnrCoelYpgaCU2y3Hs1lVe2MnQf49DSjeme3X1naNzDwB3CM4QxOhJKi8rO4MKEcjJGbhCGaUxxwk-P-2UTsC193sIGcEwuQQTQjBhPKVX4GtZya2tt5Gsi2gt3VZ3uojmdWdzqTrtrCyj9U472R6ijR_Axc5W4a5-ocoq1-QD9KnbzhY6erdKl6X2N-DCyNLr2-Ocgs3L83rxFq8-XpeL-SqWhMAuTlChETHGcMMRSfOEMMZZAjFVhieK8JTAjEGeZRKF-KhQlKUS6xQVKTFpQqbgYfRtXfPda9-Jyvohgqx103uBKaOIc4xJQGcjGjJ777QRrbOVdAeBoBjaFGOb4thmENwfvfu80sUJ_6svAI8jEIRi3_SuDq_-5_YD9mV-Gw</recordid><startdate>20201209</startdate><enddate>20201209</enddate><creator>Park, Seong-Cheol</creator><creator>Ko, Changgon</creator><creator>Hyeon, Hyejin</creator><creator>Jang, Mi-Kyeong</creator><creator>Lee, Dongwon</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/0000-0003-3972-7197</orcidid><orcidid>https://orcid.org/0000-0002-2833-3216</orcidid><orcidid>https://orcid.org/0000-0001-9051-0183</orcidid><orcidid>https://orcid.org/0000-0002-3816-5332</orcidid><orcidid>https://orcid.org/0000-0003-3035-6342</orcidid></search><sort><creationdate>20201209</creationdate><title>Imaging and Targeted Antibacterial Therapy Using Chimeric Antimicrobial Peptide Micelles</title><author>Park, Seong-Cheol ; Ko, Changgon ; Hyeon, Hyejin ; Jang, Mi-Kyeong ; Lee, Dongwon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a330t-51de13fff8f8137b5366865024cf85c38730960899a10631dc467a2e71d73f753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Antimicrobial Cationic Peptides - chemistry</topic><topic>Antimicrobial Cationic Peptides - pharmacology</topic><topic>Antimicrobial Cationic Peptides - therapeutic use</topic><topic>Biocompatible Materials - chemistry</topic><topic>Biocompatible Materials - pharmacology</topic><topic>Biocompatible Materials - therapeutic use</topic><topic>Biofilms - drug effects</topic><topic>Biological and Medical Applications of Materials and Interfaces</topic><topic>Disease Models, Animal</topic><topic>Drug Design</topic><topic>Drug Resistance, Bacterial - drug effects</topic><topic>Female</topic><topic>Gram-Negative Bacteria - drug effects</topic><topic>Gram-Negative Bacteria - physiology</topic><topic>Gram-Positive Bacteria - drug effects</topic><topic>Gram-Positive Bacteria - physiology</topic><topic>Hemolysis - drug effects</topic><topic>Lung Diseases - drug therapy</topic><topic>Lung Diseases - microbiology</topic><topic>Lung Diseases - pathology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Micelles</topic><topic>Rats</topic><topic>Soft Tissue Injuries - drug therapy</topic><topic>Soft Tissue Injuries - microbiology</topic><topic>Soft Tissue Injuries - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Seong-Cheol</creatorcontrib><creatorcontrib>Ko, Changgon</creatorcontrib><creatorcontrib>Hyeon, Hyejin</creatorcontrib><creatorcontrib>Jang, Mi-Kyeong</creatorcontrib><creatorcontrib>Lee, Dongwon</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>Park, Seong-Cheol</au><au>Ko, Changgon</au><au>Hyeon, Hyejin</au><au>Jang, Mi-Kyeong</au><au>Lee, Dongwon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Imaging and Targeted Antibacterial Therapy Using Chimeric Antimicrobial Peptide Micelles</atitle><jtitle>ACS applied materials & interfaces</jtitle><addtitle>ACS Appl. Mater. Interfaces</addtitle><date>2020-12-09</date><risdate>2020</risdate><volume>12</volume><issue>49</issue><spage>54306</spage><epage>54315</epage><pages>54306-54315</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><abstract>Infectious diseases induced by multidrug-resistant bacteria are a challenging problem in medicine because of global rise in the drug resistance to pathogenic bacteria. Despite great efforts on the development of antibiotics and antimicrobial agents, there is still a great need to develop a strategy to early detect bacterial infections and eradicate bacteria effectively and simultaneously. The innate immune systems of various organisms produce antimicrobial peptides, which kill a broad range of bacteria with minimal cytotoxicity to mammalian cells. Therefore, antimicrobial peptides have recently attracted increasing attention as an alternative to conventional antibiotics in antibacterial medications. Here, we report a new family of antibacterial agents, which is formulated from self-assembly of a chimeric antimicrobial lipopeptide (DSPE-HnMc) and amphiphilic biodegradable polymers. HnMc micelles could effectively bind the bacterial membrane to kill a wide spectrum of bacteria and bacterial biofilms. In the studies of mouse models of drug-resistant bacterial infections, HnMc micelles could target bacterial infections with high specificity and also kill drug-resistant bacteria effectively, demonstrating the great potential of HnMc micelles as imaging and targeted antibacterial agents. These findings also provide new insight into the design of antimicrobial peptide-based nanomedicine for detection and treatment of bacterial infections.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>33236874</pmid><doi>10.1021/acsami.0c13083</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-3972-7197</orcidid><orcidid>https://orcid.org/0000-0002-2833-3216</orcidid><orcidid>https://orcid.org/0000-0001-9051-0183</orcidid><orcidid>https://orcid.org/0000-0002-3816-5332</orcidid><orcidid>https://orcid.org/0000-0003-3035-6342</orcidid></addata></record> |
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subjects | Animals Antimicrobial Cationic Peptides - chemistry Antimicrobial Cationic Peptides - pharmacology Antimicrobial Cationic Peptides - therapeutic use Biocompatible Materials - chemistry Biocompatible Materials - pharmacology Biocompatible Materials - therapeutic use Biofilms - drug effects Biological and Medical Applications of Materials and Interfaces Disease Models, Animal Drug Design Drug Resistance, Bacterial - drug effects Female Gram-Negative Bacteria - drug effects Gram-Negative Bacteria - physiology Gram-Positive Bacteria - drug effects Gram-Positive Bacteria - physiology Hemolysis - drug effects Lung Diseases - drug therapy Lung Diseases - microbiology Lung Diseases - pathology Mice Mice, Inbred BALB C Micelles Rats Soft Tissue Injuries - drug therapy Soft Tissue Injuries - microbiology Soft Tissue Injuries - pathology |
title | Imaging and Targeted Antibacterial Therapy Using Chimeric Antimicrobial Peptide Micelles |
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