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Sprayed PAA-CaO(2) nanoparticles combined with calcium ions and reactive oxygen species for antibacterial and wound healing

The most common socioeconomic healthcare issues in clinical are burns, surgical incisions and other skin injuries. Skin lesion healing can be achieved with nanomedicines and other drug application techniques. This study developed a nano-spray based on cross-linked amorphous calcium peroxide (CaO(2))...

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Autores principales: Yu, Hong, Sun, Jiale, She, Kepeng, Lv, Mingqi, Zhang, Yiqiao, Xiao, Yawen, Liu, Yangkun, Han, Changhao, Xu, Xinyue, Yang, Shuqing, Wang, Guixue, Zang, Guangchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503269/
https://www.ncbi.nlm.nih.gov/pubmed/37719928
http://dx.doi.org/10.1093/rb/rbad071
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author Yu, Hong
Sun, Jiale
She, Kepeng
Lv, Mingqi
Zhang, Yiqiao
Xiao, Yawen
Liu, Yangkun
Han, Changhao
Xu, Xinyue
Yang, Shuqing
Wang, Guixue
Zang, Guangchao
author_facet Yu, Hong
Sun, Jiale
She, Kepeng
Lv, Mingqi
Zhang, Yiqiao
Xiao, Yawen
Liu, Yangkun
Han, Changhao
Xu, Xinyue
Yang, Shuqing
Wang, Guixue
Zang, Guangchao
author_sort Yu, Hong
collection PubMed
description The most common socioeconomic healthcare issues in clinical are burns, surgical incisions and other skin injuries. Skin lesion healing can be achieved with nanomedicines and other drug application techniques. This study developed a nano-spray based on cross-linked amorphous calcium peroxide (CaO(2)) nanoparticles of polyacrylic acid (PAA) for treating skin wounds (PAA-CaO(2) nanoparticles). CaO(2) serves as a ‘drug’ precursor, steadily and continuously releasing calcium ions (Ca(2+)) and hydrogen peroxide (H(2)O(2)) under mildly acidic conditions, while PAA-CaO(2) nanoparticles exhibited good spray behavior in aqueous form. Tests demonstrated that PAA-CaO(2) nanoparticles exhibited low cytotoxicity and allowed L929 cells proliferation and migration in vitro. The effectiveness of PAA-CaO(2) nanoparticles in promoting wound healing and inhibiting bacterial growth in vivo was assessed in SD rats using full-thickness skin defect and Staphylococcus aureus (S.aureus)-infected wound models based thereon. The results revealed that PAA-CaO(2) nanoparticles demonstrated significant advantages in both aspects. Notably, the infected rats’ skin defects healed in 12 days. The benefits are linked to the functional role of Ca(2+) coalesces with H(2)O(2) as known antibacterial and healing-promoted agents. Therefore, we developed nanoscale PAA-CaO(2) sprays to prevent bacterial development and heal skin lesions.
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spelling pubmed-105032692023-09-16 Sprayed PAA-CaO(2) nanoparticles combined with calcium ions and reactive oxygen species for antibacterial and wound healing Yu, Hong Sun, Jiale She, Kepeng Lv, Mingqi Zhang, Yiqiao Xiao, Yawen Liu, Yangkun Han, Changhao Xu, Xinyue Yang, Shuqing Wang, Guixue Zang, Guangchao Regen Biomater Research Article The most common socioeconomic healthcare issues in clinical are burns, surgical incisions and other skin injuries. Skin lesion healing can be achieved with nanomedicines and other drug application techniques. This study developed a nano-spray based on cross-linked amorphous calcium peroxide (CaO(2)) nanoparticles of polyacrylic acid (PAA) for treating skin wounds (PAA-CaO(2) nanoparticles). CaO(2) serves as a ‘drug’ precursor, steadily and continuously releasing calcium ions (Ca(2+)) and hydrogen peroxide (H(2)O(2)) under mildly acidic conditions, while PAA-CaO(2) nanoparticles exhibited good spray behavior in aqueous form. Tests demonstrated that PAA-CaO(2) nanoparticles exhibited low cytotoxicity and allowed L929 cells proliferation and migration in vitro. The effectiveness of PAA-CaO(2) nanoparticles in promoting wound healing and inhibiting bacterial growth in vivo was assessed in SD rats using full-thickness skin defect and Staphylococcus aureus (S.aureus)-infected wound models based thereon. The results revealed that PAA-CaO(2) nanoparticles demonstrated significant advantages in both aspects. Notably, the infected rats’ skin defects healed in 12 days. The benefits are linked to the functional role of Ca(2+) coalesces with H(2)O(2) as known antibacterial and healing-promoted agents. Therefore, we developed nanoscale PAA-CaO(2) sprays to prevent bacterial development and heal skin lesions. Oxford University Press 2023-08-21 /pmc/articles/PMC10503269/ /pubmed/37719928 http://dx.doi.org/10.1093/rb/rbad071 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yu, Hong
Sun, Jiale
She, Kepeng
Lv, Mingqi
Zhang, Yiqiao
Xiao, Yawen
Liu, Yangkun
Han, Changhao
Xu, Xinyue
Yang, Shuqing
Wang, Guixue
Zang, Guangchao
Sprayed PAA-CaO(2) nanoparticles combined with calcium ions and reactive oxygen species for antibacterial and wound healing
title Sprayed PAA-CaO(2) nanoparticles combined with calcium ions and reactive oxygen species for antibacterial and wound healing
title_full Sprayed PAA-CaO(2) nanoparticles combined with calcium ions and reactive oxygen species for antibacterial and wound healing
title_fullStr Sprayed PAA-CaO(2) nanoparticles combined with calcium ions and reactive oxygen species for antibacterial and wound healing
title_full_unstemmed Sprayed PAA-CaO(2) nanoparticles combined with calcium ions and reactive oxygen species for antibacterial and wound healing
title_short Sprayed PAA-CaO(2) nanoparticles combined with calcium ions and reactive oxygen species for antibacterial and wound healing
title_sort sprayed paa-cao(2) nanoparticles combined with calcium ions and reactive oxygen species for antibacterial and wound healing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503269/
https://www.ncbi.nlm.nih.gov/pubmed/37719928
http://dx.doi.org/10.1093/rb/rbad071
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