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Pulmonary delivery of mucus-traversing PF127-modified silk fibroin nanoparticles loading with quercetin for lung cancer therapy

The mucosal barrier remains a major barrier in the pulmonary drug delivery system, as mucociliary clearance in the airway accelerates the removal of inhaled nanoparticles (NPs). Herein, we designed and developed the inhalable Pluronic F127-modified silk fibroin NPs loading with quercetin (marked as...

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Autores principales: Tang, Yu, Zhang, Lanfang, Sun, Rui, Luo, Baiyi, Zhou, Yu, Zhang, Yan, Liang, Yuqi, Xiao, Bo, Wang, Chenhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shenyang Pharmaceutical University 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450418/
https://www.ncbi.nlm.nih.gov/pubmed/37635802
http://dx.doi.org/10.1016/j.ajps.2023.100833
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author Tang, Yu
Zhang, Lanfang
Sun, Rui
Luo, Baiyi
Zhou, Yu
Zhang, Yan
Liang, Yuqi
Xiao, Bo
Wang, Chenhui
author_facet Tang, Yu
Zhang, Lanfang
Sun, Rui
Luo, Baiyi
Zhou, Yu
Zhang, Yan
Liang, Yuqi
Xiao, Bo
Wang, Chenhui
author_sort Tang, Yu
collection PubMed
description The mucosal barrier remains a major barrier in the pulmonary drug delivery system, as mucociliary clearance in the airway accelerates the removal of inhaled nanoparticles (NPs). Herein, we designed and developed the inhalable Pluronic F127-modified silk fibroin NPs loading with quercetin (marked as QR-SF (PF127) NPs), aiming to solve the airway mucus barrier and improve the cancer therapeutic effect of QR. The PF127 coating on the SF NPs could attenuate the interaction between NPs and mucin proteins, thus facilitating the diffusion of SF(PF127) NPs in the mucus layer. The QR-SF (PF127) NPs had particle sizes of approximately 200 nm with negatively charged surfaces and showed constant drug release properties. Fluorescence recovery after photobleaching (FRAP) assay and transepithelial transport test showed that QR-SF (PF127) NPs exhibited superior mucus-penetrating ability in artificial mucus and monolayer Calu-3 cell model. Notably, a large amount of QR-SF (PF127) NPs distributed uniformly in the mice airway section, indicating the good retention of NPs in the respiratory tract. The mice melanoma lung metastasis model was established, and the therapeutic effect of QR-SF (PF127) NPs was significantly improved in vivo. PF127-modified SF NPs may be a promising strategy to attenuate the interaction with mucin proteins and enhance mucus penetration efficiency in the pulmonary drug delivery system.
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spelling pubmed-104504182023-08-26 Pulmonary delivery of mucus-traversing PF127-modified silk fibroin nanoparticles loading with quercetin for lung cancer therapy Tang, Yu Zhang, Lanfang Sun, Rui Luo, Baiyi Zhou, Yu Zhang, Yan Liang, Yuqi Xiao, Bo Wang, Chenhui Asian J Pharm Sci Original Research Paper The mucosal barrier remains a major barrier in the pulmonary drug delivery system, as mucociliary clearance in the airway accelerates the removal of inhaled nanoparticles (NPs). Herein, we designed and developed the inhalable Pluronic F127-modified silk fibroin NPs loading with quercetin (marked as QR-SF (PF127) NPs), aiming to solve the airway mucus barrier and improve the cancer therapeutic effect of QR. The PF127 coating on the SF NPs could attenuate the interaction between NPs and mucin proteins, thus facilitating the diffusion of SF(PF127) NPs in the mucus layer. The QR-SF (PF127) NPs had particle sizes of approximately 200 nm with negatively charged surfaces and showed constant drug release properties. Fluorescence recovery after photobleaching (FRAP) assay and transepithelial transport test showed that QR-SF (PF127) NPs exhibited superior mucus-penetrating ability in artificial mucus and monolayer Calu-3 cell model. Notably, a large amount of QR-SF (PF127) NPs distributed uniformly in the mice airway section, indicating the good retention of NPs in the respiratory tract. The mice melanoma lung metastasis model was established, and the therapeutic effect of QR-SF (PF127) NPs was significantly improved in vivo. PF127-modified SF NPs may be a promising strategy to attenuate the interaction with mucin proteins and enhance mucus penetration efficiency in the pulmonary drug delivery system. Shenyang Pharmaceutical University 2023-07 2023-07-28 /pmc/articles/PMC10450418/ /pubmed/37635802 http://dx.doi.org/10.1016/j.ajps.2023.100833 Text en © 2023 Shenyang Pharmaceutical University. Published 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 Research Paper
Tang, Yu
Zhang, Lanfang
Sun, Rui
Luo, Baiyi
Zhou, Yu
Zhang, Yan
Liang, Yuqi
Xiao, Bo
Wang, Chenhui
Pulmonary delivery of mucus-traversing PF127-modified silk fibroin nanoparticles loading with quercetin for lung cancer therapy
title Pulmonary delivery of mucus-traversing PF127-modified silk fibroin nanoparticles loading with quercetin for lung cancer therapy
title_full Pulmonary delivery of mucus-traversing PF127-modified silk fibroin nanoparticles loading with quercetin for lung cancer therapy
title_fullStr Pulmonary delivery of mucus-traversing PF127-modified silk fibroin nanoparticles loading with quercetin for lung cancer therapy
title_full_unstemmed Pulmonary delivery of mucus-traversing PF127-modified silk fibroin nanoparticles loading with quercetin for lung cancer therapy
title_short Pulmonary delivery of mucus-traversing PF127-modified silk fibroin nanoparticles loading with quercetin for lung cancer therapy
title_sort pulmonary delivery of mucus-traversing pf127-modified silk fibroin nanoparticles loading with quercetin for lung cancer therapy
topic Original Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450418/
https://www.ncbi.nlm.nih.gov/pubmed/37635802
http://dx.doi.org/10.1016/j.ajps.2023.100833
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