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Development of a Temperature-Responsive Hydrogel Incorporating PVA into NIPAAm for Controllable Drug Release in Skin Regeneration

[Image: see text] Melanoma, a highly malignant and aggressive form of skin cancer, poses a significant global health threat, with limited treatment options and potential side effects. In this study, we developed a temperature-responsive hydrogel for skin regeneration with a controllable drug release...

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Autores principales: Choi, Jae Hwan, Lee, Jae Seo, Yang, Dae Hyeok, Nah, Haram, Min, Sung Jun, Lee, Seung Yeon, Yoo, Ji Hye, Chun, Heung Jae, Moon, Ho-Jin, Hong, Young Ki, Heo, Dong Nyoung, Kwon, Il Keun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666273/
https://www.ncbi.nlm.nih.gov/pubmed/38027389
http://dx.doi.org/10.1021/acsomega.3c06291
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author Choi, Jae Hwan
Lee, Jae Seo
Yang, Dae Hyeok
Nah, Haram
Min, Sung Jun
Lee, Seung Yeon
Yoo, Ji Hye
Chun, Heung Jae
Moon, Ho-Jin
Hong, Young Ki
Heo, Dong Nyoung
Kwon, Il Keun
author_facet Choi, Jae Hwan
Lee, Jae Seo
Yang, Dae Hyeok
Nah, Haram
Min, Sung Jun
Lee, Seung Yeon
Yoo, Ji Hye
Chun, Heung Jae
Moon, Ho-Jin
Hong, Young Ki
Heo, Dong Nyoung
Kwon, Il Keun
author_sort Choi, Jae Hwan
collection PubMed
description [Image: see text] Melanoma, a highly malignant and aggressive form of skin cancer, poses a significant global health threat, with limited treatment options and potential side effects. In this study, we developed a temperature-responsive hydrogel for skin regeneration with a controllable drug release. The hydrogel was fabricated using an interpenetrating polymer network (IPN) of N-isopropylacrylamide (NIPAAm) and poly(vinyl alcohol) (PVA). PVA was chosen for its adhesive properties, biocompatibility, and ability to address hydrophobicity issues associated with NIPAAm. The hydrogel was loaded with doxorubicin (DOX), an anticancer drug, for the treatment of melanoma. The NIPAAm-PVA (N–P) hydrogel demonstrated temperature-responsive behavior with a lower critical solution temperature (LCST) around 34 °C. The addition of PVA led to increased porosity and faster drug release. In vitro biocompatibility tests showed nontoxicity and supported cell proliferation. The N–P hydrogel exhibited effective anticancer effects on melanoma cells due to its rapid drug release behavior. This N–P hydrogel system shows great promise for controlled drug delivery and potential applications in skin regeneration and cancer treatment. Further research, including in vivo studies, will be essential to advance this hydrogel system toward clinical translation and impactful advancements in regenerative medicine and cancer therapeutics.
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spelling pubmed-106662732023-11-07 Development of a Temperature-Responsive Hydrogel Incorporating PVA into NIPAAm for Controllable Drug Release in Skin Regeneration Choi, Jae Hwan Lee, Jae Seo Yang, Dae Hyeok Nah, Haram Min, Sung Jun Lee, Seung Yeon Yoo, Ji Hye Chun, Heung Jae Moon, Ho-Jin Hong, Young Ki Heo, Dong Nyoung Kwon, Il Keun ACS Omega [Image: see text] Melanoma, a highly malignant and aggressive form of skin cancer, poses a significant global health threat, with limited treatment options and potential side effects. In this study, we developed a temperature-responsive hydrogel for skin regeneration with a controllable drug release. The hydrogel was fabricated using an interpenetrating polymer network (IPN) of N-isopropylacrylamide (NIPAAm) and poly(vinyl alcohol) (PVA). PVA was chosen for its adhesive properties, biocompatibility, and ability to address hydrophobicity issues associated with NIPAAm. The hydrogel was loaded with doxorubicin (DOX), an anticancer drug, for the treatment of melanoma. The NIPAAm-PVA (N–P) hydrogel demonstrated temperature-responsive behavior with a lower critical solution temperature (LCST) around 34 °C. The addition of PVA led to increased porosity and faster drug release. In vitro biocompatibility tests showed nontoxicity and supported cell proliferation. The N–P hydrogel exhibited effective anticancer effects on melanoma cells due to its rapid drug release behavior. This N–P hydrogel system shows great promise for controlled drug delivery and potential applications in skin regeneration and cancer treatment. Further research, including in vivo studies, will be essential to advance this hydrogel system toward clinical translation and impactful advancements in regenerative medicine and cancer therapeutics. American Chemical Society 2023-11-07 /pmc/articles/PMC10666273/ /pubmed/38027389 http://dx.doi.org/10.1021/acsomega.3c06291 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Choi, Jae Hwan
Lee, Jae Seo
Yang, Dae Hyeok
Nah, Haram
Min, Sung Jun
Lee, Seung Yeon
Yoo, Ji Hye
Chun, Heung Jae
Moon, Ho-Jin
Hong, Young Ki
Heo, Dong Nyoung
Kwon, Il Keun
Development of a Temperature-Responsive Hydrogel Incorporating PVA into NIPAAm for Controllable Drug Release in Skin Regeneration
title Development of a Temperature-Responsive Hydrogel Incorporating PVA into NIPAAm for Controllable Drug Release in Skin Regeneration
title_full Development of a Temperature-Responsive Hydrogel Incorporating PVA into NIPAAm for Controllable Drug Release in Skin Regeneration
title_fullStr Development of a Temperature-Responsive Hydrogel Incorporating PVA into NIPAAm for Controllable Drug Release in Skin Regeneration
title_full_unstemmed Development of a Temperature-Responsive Hydrogel Incorporating PVA into NIPAAm for Controllable Drug Release in Skin Regeneration
title_short Development of a Temperature-Responsive Hydrogel Incorporating PVA into NIPAAm for Controllable Drug Release in Skin Regeneration
title_sort development of a temperature-responsive hydrogel incorporating pva into nipaam for controllable drug release in skin regeneration
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666273/
https://www.ncbi.nlm.nih.gov/pubmed/38027389
http://dx.doi.org/10.1021/acsomega.3c06291
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