Cargando…

Mesoporous polydopamine nanoparticles carrying peptide RL-QN15 show potential for skin wound therapy

BACKGROUND: Skin wound healing remains a considerable clinical challenge, thus stressing the urgent need for the development of new interventions to promote repair. Recent researches indicate that both peptides and nanoparticles may be potential therapies for the treatment of skin wounds. METHODS: I...

Descripción completa

Detalles Bibliográficos
Autores principales: Qin, Pan, Meng, Yi, Yang, Ying, Gou, Xinyu, Liu, Naixin, Yin, Saige, Hu, Yan, Sun, Huiling, Fu, Zhe, Wang, Yinglei, Li, Xiaojie, Tang, Jing, Wang, Ying, Deng, Ziwei, Yang, Xinwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501717/
https://www.ncbi.nlm.nih.gov/pubmed/34627291
http://dx.doi.org/10.1186/s12951-021-01051-8
_version_ 1784580745092661248
author Qin, Pan
Meng, Yi
Yang, Ying
Gou, Xinyu
Liu, Naixin
Yin, Saige
Hu, Yan
Sun, Huiling
Fu, Zhe
Wang, Yinglei
Li, Xiaojie
Tang, Jing
Wang, Ying
Deng, Ziwei
Yang, Xinwang
author_facet Qin, Pan
Meng, Yi
Yang, Ying
Gou, Xinyu
Liu, Naixin
Yin, Saige
Hu, Yan
Sun, Huiling
Fu, Zhe
Wang, Yinglei
Li, Xiaojie
Tang, Jing
Wang, Ying
Deng, Ziwei
Yang, Xinwang
author_sort Qin, Pan
collection PubMed
description BACKGROUND: Skin wound healing remains a considerable clinical challenge, thus stressing the urgent need for the development of new interventions to promote repair. Recent researches indicate that both peptides and nanoparticles may be potential therapies for the treatment of skin wounds. METHODS: In the current study, the mesoporous polydopamine (MPDA) nanoparticles were prepared and the peptide RL-QN15 that was previously identified from amphibian skin secretions and exhibited significant potential as a novel prohealing agent was successfully loaded onto the MPDA nanoparticles, which was confirmed by results of analysis of scanning electron microscopy and fourier transform infrared spectroscopy. The encapsulation efficiency and sustained release rate of RL-QN15 from the nanocomposites were determined. The prohealing potency of nanocomposites were evaluated by full-thickness injured wounds in both mice and swine and burn wounds in mice. RESULTS: Our results indicated that, compared with RL-QN15 alone, the prohealing potency of nanocomposites of MPDA and RL-QN15 in the full-thickness injured wounds and burn wounds in mice was increased by up to 50 times through the slow release of RL-QN15. Moreover, the load on the MPDA obviously increased the prohealing activities of RL-QN15 in full-thickness injured wounds in swine. In addition, the obvious increase in the prohealing potency of nanocomposites of MPDA and RL-QN15 was also proved by the results from histological analysis. CONCLUSIONS: Based on our knowledge, this is the first research to report that the load of MPDA nanoparticles could significantly increase the prohealing potency of peptide and hence highlighted the promising potential of MPDA nanoparticles-carrying peptide RL-QN15 for skin wound therapy. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-01051-8.
format Online
Article
Text
id pubmed-8501717
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-85017172021-10-20 Mesoporous polydopamine nanoparticles carrying peptide RL-QN15 show potential for skin wound therapy Qin, Pan Meng, Yi Yang, Ying Gou, Xinyu Liu, Naixin Yin, Saige Hu, Yan Sun, Huiling Fu, Zhe Wang, Yinglei Li, Xiaojie Tang, Jing Wang, Ying Deng, Ziwei Yang, Xinwang J Nanobiotechnology Research BACKGROUND: Skin wound healing remains a considerable clinical challenge, thus stressing the urgent need for the development of new interventions to promote repair. Recent researches indicate that both peptides and nanoparticles may be potential therapies for the treatment of skin wounds. METHODS: In the current study, the mesoporous polydopamine (MPDA) nanoparticles were prepared and the peptide RL-QN15 that was previously identified from amphibian skin secretions and exhibited significant potential as a novel prohealing agent was successfully loaded onto the MPDA nanoparticles, which was confirmed by results of analysis of scanning electron microscopy and fourier transform infrared spectroscopy. The encapsulation efficiency and sustained release rate of RL-QN15 from the nanocomposites were determined. The prohealing potency of nanocomposites were evaluated by full-thickness injured wounds in both mice and swine and burn wounds in mice. RESULTS: Our results indicated that, compared with RL-QN15 alone, the prohealing potency of nanocomposites of MPDA and RL-QN15 in the full-thickness injured wounds and burn wounds in mice was increased by up to 50 times through the slow release of RL-QN15. Moreover, the load on the MPDA obviously increased the prohealing activities of RL-QN15 in full-thickness injured wounds in swine. In addition, the obvious increase in the prohealing potency of nanocomposites of MPDA and RL-QN15 was also proved by the results from histological analysis. CONCLUSIONS: Based on our knowledge, this is the first research to report that the load of MPDA nanoparticles could significantly increase the prohealing potency of peptide and hence highlighted the promising potential of MPDA nanoparticles-carrying peptide RL-QN15 for skin wound therapy. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-01051-8. BioMed Central 2021-10-09 /pmc/articles/PMC8501717/ /pubmed/34627291 http://dx.doi.org/10.1186/s12951-021-01051-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Qin, Pan
Meng, Yi
Yang, Ying
Gou, Xinyu
Liu, Naixin
Yin, Saige
Hu, Yan
Sun, Huiling
Fu, Zhe
Wang, Yinglei
Li, Xiaojie
Tang, Jing
Wang, Ying
Deng, Ziwei
Yang, Xinwang
Mesoporous polydopamine nanoparticles carrying peptide RL-QN15 show potential for skin wound therapy
title Mesoporous polydopamine nanoparticles carrying peptide RL-QN15 show potential for skin wound therapy
title_full Mesoporous polydopamine nanoparticles carrying peptide RL-QN15 show potential for skin wound therapy
title_fullStr Mesoporous polydopamine nanoparticles carrying peptide RL-QN15 show potential for skin wound therapy
title_full_unstemmed Mesoporous polydopamine nanoparticles carrying peptide RL-QN15 show potential for skin wound therapy
title_short Mesoporous polydopamine nanoparticles carrying peptide RL-QN15 show potential for skin wound therapy
title_sort mesoporous polydopamine nanoparticles carrying peptide rl-qn15 show potential for skin wound therapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501717/
https://www.ncbi.nlm.nih.gov/pubmed/34627291
http://dx.doi.org/10.1186/s12951-021-01051-8
work_keys_str_mv AT qinpan mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT mengyi mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT yangying mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT gouxinyu mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT liunaixin mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT yinsaige mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT huyan mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT sunhuiling mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT fuzhe mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT wangyinglei mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT lixiaojie mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT tangjing mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT wangying mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT dengziwei mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy
AT yangxinwang mesoporouspolydopaminenanoparticlescarryingpeptiderlqn15showpotentialforskinwoundtherapy