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Combined Biomimetic MOF-RVG15 Nanoformulation Efficient Over BBB for Effective Anti-Glioblastoma in Mice Model

INTRODUCTION: The blood–brain barrier (BBB) is a key obstacle to the delivery of drugs into the brain. Therefore, it is essential to develop an advanced drug delivery nanoplatform to solve this problem. We previously screened a small rabies virus glycoprotein 15 (RVG(15)) peptide with 15 amino acids...

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Autores principales: Wu, Hao, Liu, Yanhong, Chen, Liqing, Wang, Shuangqing, Liu, Chao, Zhao, Heming, Jin, Mingji, Chang, Shuangyan, Quan, Xiuquan, Cui, Minhu, Wan, Hongshuang, Gao, Zhonggao, Huang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762271/
https://www.ncbi.nlm.nih.gov/pubmed/36545220
http://dx.doi.org/10.2147/IJN.S387715
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author Wu, Hao
Liu, Yanhong
Chen, Liqing
Wang, Shuangqing
Liu, Chao
Zhao, Heming
Jin, Mingji
Chang, Shuangyan
Quan, Xiuquan
Cui, Minhu
Wan, Hongshuang
Gao, Zhonggao
Huang, Wei
author_facet Wu, Hao
Liu, Yanhong
Chen, Liqing
Wang, Shuangqing
Liu, Chao
Zhao, Heming
Jin, Mingji
Chang, Shuangyan
Quan, Xiuquan
Cui, Minhu
Wan, Hongshuang
Gao, Zhonggao
Huang, Wei
author_sort Wu, Hao
collection PubMed
description INTRODUCTION: The blood–brain barrier (BBB) is a key obstacle to the delivery of drugs into the brain. Therefore, it is essential to develop an advanced drug delivery nanoplatform to solve this problem. We previously screened a small rabies virus glycoprotein 15 (RVG(15)) peptide with 15 amino acids and observed that most of the RVG(15)-modified nanoparticles entered the brain within 1 h of administration. The high BBB penetrability gives RVG(15) great potential for brain-targeted drug delivery systems. Moreover, a multifunctional integrated nanoplatform with a high drug-loading capacity, tunable functionality, and controlled drug release is crucial for tumor treatment. Zeolitic imidazolate framework (ZIF-8) is a promising nanodrug delivery system. METHODS: Inspired by the biomimetic concept, we designed RVG(15)-coated biomimetic ZIF-8 nanoparticles (RVG(15)-PEG@DTX@ZIF-8) for docetaxel (DTX) delivery to achieve efficient glioblastoma elimination in mice. This bionic nanotherapeutic system was prepared by one-pot encapsulation, followed by coating with RVG(15)-PEG conjugates. The size, morphology, stability, drug-loading capacity, and release of RVG(15)-PEG@DTX@ZIF-8 were thoroughly investigated. Additionally, we performed in vitro evaluation, cell uptake capacity, BBB penetration, and anti-migratory ability. We also conducted an in vivo evaluation of the biodistribution and anti-glioma efficacy of this bionic nanotherapeutic system in a mouse mode. RESULTS: In vitro studies showed that, this bionic nanotherapeutic system exhibited excellent targeting efficiency and safety in HBMECs and C6 cells and high efficiency in crossing the BBB. Furthermore, the nanoparticles cause rapid DTX accumulation in the brain, allowing deeper penetration into glioma tumors. In vivo antitumor assay results indicated that RVG(15)-PEG@DTX@ZIF-8 significantly inhibited glioma growth and metastasis, thereby improving the survival of tumor-bearing mice. CONCLUSION: Our study demonstrates that our bionic nanotherapeutic system using RVG(15) peptides is a promising and powerful tool for crossing the BBB and treating glioblastoma.
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spelling pubmed-97622712022-12-20 Combined Biomimetic MOF-RVG15 Nanoformulation Efficient Over BBB for Effective Anti-Glioblastoma in Mice Model Wu, Hao Liu, Yanhong Chen, Liqing Wang, Shuangqing Liu, Chao Zhao, Heming Jin, Mingji Chang, Shuangyan Quan, Xiuquan Cui, Minhu Wan, Hongshuang Gao, Zhonggao Huang, Wei Int J Nanomedicine Original Research INTRODUCTION: The blood–brain barrier (BBB) is a key obstacle to the delivery of drugs into the brain. Therefore, it is essential to develop an advanced drug delivery nanoplatform to solve this problem. We previously screened a small rabies virus glycoprotein 15 (RVG(15)) peptide with 15 amino acids and observed that most of the RVG(15)-modified nanoparticles entered the brain within 1 h of administration. The high BBB penetrability gives RVG(15) great potential for brain-targeted drug delivery systems. Moreover, a multifunctional integrated nanoplatform with a high drug-loading capacity, tunable functionality, and controlled drug release is crucial for tumor treatment. Zeolitic imidazolate framework (ZIF-8) is a promising nanodrug delivery system. METHODS: Inspired by the biomimetic concept, we designed RVG(15)-coated biomimetic ZIF-8 nanoparticles (RVG(15)-PEG@DTX@ZIF-8) for docetaxel (DTX) delivery to achieve efficient glioblastoma elimination in mice. This bionic nanotherapeutic system was prepared by one-pot encapsulation, followed by coating with RVG(15)-PEG conjugates. The size, morphology, stability, drug-loading capacity, and release of RVG(15)-PEG@DTX@ZIF-8 were thoroughly investigated. Additionally, we performed in vitro evaluation, cell uptake capacity, BBB penetration, and anti-migratory ability. We also conducted an in vivo evaluation of the biodistribution and anti-glioma efficacy of this bionic nanotherapeutic system in a mouse mode. RESULTS: In vitro studies showed that, this bionic nanotherapeutic system exhibited excellent targeting efficiency and safety in HBMECs and C6 cells and high efficiency in crossing the BBB. Furthermore, the nanoparticles cause rapid DTX accumulation in the brain, allowing deeper penetration into glioma tumors. In vivo antitumor assay results indicated that RVG(15)-PEG@DTX@ZIF-8 significantly inhibited glioma growth and metastasis, thereby improving the survival of tumor-bearing mice. CONCLUSION: Our study demonstrates that our bionic nanotherapeutic system using RVG(15) peptides is a promising and powerful tool for crossing the BBB and treating glioblastoma. Dove 2022-12-15 /pmc/articles/PMC9762271/ /pubmed/36545220 http://dx.doi.org/10.2147/IJN.S387715 Text en © 2022 Wu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wu, Hao
Liu, Yanhong
Chen, Liqing
Wang, Shuangqing
Liu, Chao
Zhao, Heming
Jin, Mingji
Chang, Shuangyan
Quan, Xiuquan
Cui, Minhu
Wan, Hongshuang
Gao, Zhonggao
Huang, Wei
Combined Biomimetic MOF-RVG15 Nanoformulation Efficient Over BBB for Effective Anti-Glioblastoma in Mice Model
title Combined Biomimetic MOF-RVG15 Nanoformulation Efficient Over BBB for Effective Anti-Glioblastoma in Mice Model
title_full Combined Biomimetic MOF-RVG15 Nanoformulation Efficient Over BBB for Effective Anti-Glioblastoma in Mice Model
title_fullStr Combined Biomimetic MOF-RVG15 Nanoformulation Efficient Over BBB for Effective Anti-Glioblastoma in Mice Model
title_full_unstemmed Combined Biomimetic MOF-RVG15 Nanoformulation Efficient Over BBB for Effective Anti-Glioblastoma in Mice Model
title_short Combined Biomimetic MOF-RVG15 Nanoformulation Efficient Over BBB for Effective Anti-Glioblastoma in Mice Model
title_sort combined biomimetic mof-rvg15 nanoformulation efficient over bbb for effective anti-glioblastoma in mice model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762271/
https://www.ncbi.nlm.nih.gov/pubmed/36545220
http://dx.doi.org/10.2147/IJN.S387715
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