Cargando…

ε‐poly‐L‐lysine‐modified polydopamine nanoparticles for targeted photothermal therapy of drug‐resistant bacterial keratitis

Bacterial keratitis can lead to intraocular infection and even blindness without prompt and potent treatments. Currently, clinical abuse of antibiotics encouraged the evolution of resistant bacteria. Conventional antibiotic eye drops based keratitis treatment has been heavily restricted due to the l...

Descripción completa

Detalles Bibliográficos
Autores principales: Fan, Wenjie, Han, Haijie, Lu, Zhouyu, Huang, Yue, Zhang, Yin, Chen, Yaoyao, Zhang, Xiaobo, Ji, Jian, Yao, Ke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842021/
https://www.ncbi.nlm.nih.gov/pubmed/36684079
http://dx.doi.org/10.1002/btm2.10380
_version_ 1784870022542262272
author Fan, Wenjie
Han, Haijie
Lu, Zhouyu
Huang, Yue
Zhang, Yin
Chen, Yaoyao
Zhang, Xiaobo
Ji, Jian
Yao, Ke
author_facet Fan, Wenjie
Han, Haijie
Lu, Zhouyu
Huang, Yue
Zhang, Yin
Chen, Yaoyao
Zhang, Xiaobo
Ji, Jian
Yao, Ke
author_sort Fan, Wenjie
collection PubMed
description Bacterial keratitis can lead to intraocular infection and even blindness without prompt and potent treatments. Currently, clinical abuse of antibiotics encouraged the evolution of resistant bacteria. Conventional antibiotic eye drops based keratitis treatment has been heavily restricted due to the lack of bactericidal efficiency and easy induction of bacterial resistance. Hence, developing an effective treatment strategy for bacterial keratitis is of great significance. In this work, we investigated ε‐poly‐l‐lysine (EPL)‐modified polydopamine (PDA) nanoparticles (EPL@PDA NPs)‐mediated antibacterial photothermal therapy (aPTT), to cope with methicillin‐resistant Staphylococcus aureus (MRSA)‐induced keratitis. The surface modification of cationic peptide EPL enables EPL@PDA NPs to specifically target negatively charged MRSA and induces local hyperthermia to kill the bacteria under low ambient temperature. Under near‐infrared (NIR) irradiation, the sterilization efficiency of EPL@PDA NPs suspension for MRSA in vitro was up to 99.96%. The EPL@PDA‐mediated aPTT presented potent antibacterial efficacy in treating MRSA‐induced keratitis with little corneal epithelial cytotoxicity and good biocompatibility. In conclusion, the bacterial‐targeting aPTT platform in this work provides a prospective method for the management of MRSA‐induced refractory bacterial keratitis.
format Online
Article
Text
id pubmed-9842021
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-98420212023-01-19 ε‐poly‐L‐lysine‐modified polydopamine nanoparticles for targeted photothermal therapy of drug‐resistant bacterial keratitis Fan, Wenjie Han, Haijie Lu, Zhouyu Huang, Yue Zhang, Yin Chen, Yaoyao Zhang, Xiaobo Ji, Jian Yao, Ke Bioeng Transl Med Research Articles Bacterial keratitis can lead to intraocular infection and even blindness without prompt and potent treatments. Currently, clinical abuse of antibiotics encouraged the evolution of resistant bacteria. Conventional antibiotic eye drops based keratitis treatment has been heavily restricted due to the lack of bactericidal efficiency and easy induction of bacterial resistance. Hence, developing an effective treatment strategy for bacterial keratitis is of great significance. In this work, we investigated ε‐poly‐l‐lysine (EPL)‐modified polydopamine (PDA) nanoparticles (EPL@PDA NPs)‐mediated antibacterial photothermal therapy (aPTT), to cope with methicillin‐resistant Staphylococcus aureus (MRSA)‐induced keratitis. The surface modification of cationic peptide EPL enables EPL@PDA NPs to specifically target negatively charged MRSA and induces local hyperthermia to kill the bacteria under low ambient temperature. Under near‐infrared (NIR) irradiation, the sterilization efficiency of EPL@PDA NPs suspension for MRSA in vitro was up to 99.96%. The EPL@PDA‐mediated aPTT presented potent antibacterial efficacy in treating MRSA‐induced keratitis with little corneal epithelial cytotoxicity and good biocompatibility. In conclusion, the bacterial‐targeting aPTT platform in this work provides a prospective method for the management of MRSA‐induced refractory bacterial keratitis. John Wiley & Sons, Inc. 2022-08-04 /pmc/articles/PMC9842021/ /pubmed/36684079 http://dx.doi.org/10.1002/btm2.10380 Text en © 2022 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Fan, Wenjie
Han, Haijie
Lu, Zhouyu
Huang, Yue
Zhang, Yin
Chen, Yaoyao
Zhang, Xiaobo
Ji, Jian
Yao, Ke
ε‐poly‐L‐lysine‐modified polydopamine nanoparticles for targeted photothermal therapy of drug‐resistant bacterial keratitis
title ε‐poly‐L‐lysine‐modified polydopamine nanoparticles for targeted photothermal therapy of drug‐resistant bacterial keratitis
title_full ε‐poly‐L‐lysine‐modified polydopamine nanoparticles for targeted photothermal therapy of drug‐resistant bacterial keratitis
title_fullStr ε‐poly‐L‐lysine‐modified polydopamine nanoparticles for targeted photothermal therapy of drug‐resistant bacterial keratitis
title_full_unstemmed ε‐poly‐L‐lysine‐modified polydopamine nanoparticles for targeted photothermal therapy of drug‐resistant bacterial keratitis
title_short ε‐poly‐L‐lysine‐modified polydopamine nanoparticles for targeted photothermal therapy of drug‐resistant bacterial keratitis
title_sort ε‐poly‐l‐lysine‐modified polydopamine nanoparticles for targeted photothermal therapy of drug‐resistant bacterial keratitis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842021/
https://www.ncbi.nlm.nih.gov/pubmed/36684079
http://dx.doi.org/10.1002/btm2.10380
work_keys_str_mv AT fanwenjie epolyllysinemodifiedpolydopaminenanoparticlesfortargetedphotothermaltherapyofdrugresistantbacterialkeratitis
AT hanhaijie epolyllysinemodifiedpolydopaminenanoparticlesfortargetedphotothermaltherapyofdrugresistantbacterialkeratitis
AT luzhouyu epolyllysinemodifiedpolydopaminenanoparticlesfortargetedphotothermaltherapyofdrugresistantbacterialkeratitis
AT huangyue epolyllysinemodifiedpolydopaminenanoparticlesfortargetedphotothermaltherapyofdrugresistantbacterialkeratitis
AT zhangyin epolyllysinemodifiedpolydopaminenanoparticlesfortargetedphotothermaltherapyofdrugresistantbacterialkeratitis
AT chenyaoyao epolyllysinemodifiedpolydopaminenanoparticlesfortargetedphotothermaltherapyofdrugresistantbacterialkeratitis
AT zhangxiaobo epolyllysinemodifiedpolydopaminenanoparticlesfortargetedphotothermaltherapyofdrugresistantbacterialkeratitis
AT jijian epolyllysinemodifiedpolydopaminenanoparticlesfortargetedphotothermaltherapyofdrugresistantbacterialkeratitis
AT yaoke epolyllysinemodifiedpolydopaminenanoparticlesfortargetedphotothermaltherapyofdrugresistantbacterialkeratitis