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Inhaled curcumin mesoporous polydopamine nanoparticles against radiation pneumonitis

Radiation therapy is an effective method to kill cancer cells and shrink tumors using high-energy X-ray or γ-ray. Radiation pneumonitis (RP) is one of the most serious complications of radiation therapy for thoracic cancers, commonly leading to serious respiratory distress and poor prognosis. Here,...

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Autores principales: Chen, Ting, Zhuang, Bo, Huang, Yueqi, Liu, Yan, Yuan, Bochuan, Wang, Wanmei, Yuan, Tianyu, Du, Lina, Jin, Yiguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136532/
https://www.ncbi.nlm.nih.gov/pubmed/35646537
http://dx.doi.org/10.1016/j.apsb.2021.10.027
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author Chen, Ting
Zhuang, Bo
Huang, Yueqi
Liu, Yan
Yuan, Bochuan
Wang, Wanmei
Yuan, Tianyu
Du, Lina
Jin, Yiguang
author_facet Chen, Ting
Zhuang, Bo
Huang, Yueqi
Liu, Yan
Yuan, Bochuan
Wang, Wanmei
Yuan, Tianyu
Du, Lina
Jin, Yiguang
author_sort Chen, Ting
collection PubMed
description Radiation therapy is an effective method to kill cancer cells and shrink tumors using high-energy X-ray or γ-ray. Radiation pneumonitis (RP) is one of the most serious complications of radiation therapy for thoracic cancers, commonly leading to serious respiratory distress and poor prognosis. Here, we prepared curcumin-loaded mesoporous polydopamine nanoparticles (CMPN) for prevention and treatment of RP by pulmonary delivery. Mesoporous polydopamine nanoparticles (MPDA) were successfully synthesized with an emulsion-induced interface polymerization method and curcumin was loaded in MPDA via π‒π stacking and hydrogen bonding interaction. MPDA owned the uniform spherical morphology with numerous mesopores that disappeared after loading curcumin. More than 80% curcumin released from CMPN in 6 h and mesopores recovered. CMPN remarkably protected BEAS-2B cells from γ-ray radiation injury by inhibiting apoptosis. RP rat models were established after a single dose of 15 Gy (60)Co γ-ray radiation was performed on the chest area. Effective therapy of RP was achieved by intratracheal administration of CMPN due to free radical scavenging and anti-oxidation ability, and reduced proinflammatory cytokines, high superoxide dismutase, decreased malondialdehyde, and alleviated lung tissue damages were observed. Inhaled CMPN paves a new avenue for the treatment of RP.
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spelling pubmed-91365322022-05-28 Inhaled curcumin mesoporous polydopamine nanoparticles against radiation pneumonitis Chen, Ting Zhuang, Bo Huang, Yueqi Liu, Yan Yuan, Bochuan Wang, Wanmei Yuan, Tianyu Du, Lina Jin, Yiguang Acta Pharm Sin B Original Article Radiation therapy is an effective method to kill cancer cells and shrink tumors using high-energy X-ray or γ-ray. Radiation pneumonitis (RP) is one of the most serious complications of radiation therapy for thoracic cancers, commonly leading to serious respiratory distress and poor prognosis. Here, we prepared curcumin-loaded mesoporous polydopamine nanoparticles (CMPN) for prevention and treatment of RP by pulmonary delivery. Mesoporous polydopamine nanoparticles (MPDA) were successfully synthesized with an emulsion-induced interface polymerization method and curcumin was loaded in MPDA via π‒π stacking and hydrogen bonding interaction. MPDA owned the uniform spherical morphology with numerous mesopores that disappeared after loading curcumin. More than 80% curcumin released from CMPN in 6 h and mesopores recovered. CMPN remarkably protected BEAS-2B cells from γ-ray radiation injury by inhibiting apoptosis. RP rat models were established after a single dose of 15 Gy (60)Co γ-ray radiation was performed on the chest area. Effective therapy of RP was achieved by intratracheal administration of CMPN due to free radical scavenging and anti-oxidation ability, and reduced proinflammatory cytokines, high superoxide dismutase, decreased malondialdehyde, and alleviated lung tissue damages were observed. Inhaled CMPN paves a new avenue for the treatment of RP. Elsevier 2022-05 2021-11-05 /pmc/articles/PMC9136532/ /pubmed/35646537 http://dx.doi.org/10.1016/j.apsb.2021.10.027 Text en © 2022 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Chen, Ting
Zhuang, Bo
Huang, Yueqi
Liu, Yan
Yuan, Bochuan
Wang, Wanmei
Yuan, Tianyu
Du, Lina
Jin, Yiguang
Inhaled curcumin mesoporous polydopamine nanoparticles against radiation pneumonitis
title Inhaled curcumin mesoporous polydopamine nanoparticles against radiation pneumonitis
title_full Inhaled curcumin mesoporous polydopamine nanoparticles against radiation pneumonitis
title_fullStr Inhaled curcumin mesoporous polydopamine nanoparticles against radiation pneumonitis
title_full_unstemmed Inhaled curcumin mesoporous polydopamine nanoparticles against radiation pneumonitis
title_short Inhaled curcumin mesoporous polydopamine nanoparticles against radiation pneumonitis
title_sort inhaled curcumin mesoporous polydopamine nanoparticles against radiation pneumonitis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136532/
https://www.ncbi.nlm.nih.gov/pubmed/35646537
http://dx.doi.org/10.1016/j.apsb.2021.10.027
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