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Mechanisms of enhanced antiglioma efficacy of polysorbate 80-modified paclitaxel-loaded PLGA nanoparticles by focused ultrasound.
Li, Yingjia; Wu, Manxiang; Zhang, Nisi; Tang, Caiyun; Jiang, Peng; Liu, Xin; Yan, Fei; Zheng, Hairong.
Afiliação
  • Li Y; Department of Medicine Ultrasonics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Wu M; Department of Medicine Ultrasonics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Zhang N; Paul C. Lauterbur Research Center for Biomedical Imaging, Institute of biomedical and Health Engineering, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
  • Tang C; Biomedical Engineering Department, College of Engineering, Peking University, Beijing, China.
  • Jiang P; Paul C. Lauterbur Research Center for Biomedical Imaging, Institute of biomedical and Health Engineering, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
  • Liu X; Pharmaceutical Analysis Department, College of Pharmacy, Jiamusi University, Jiamusi, China.
  • Yan F; Shenzhen Key Laboratory of Nanobiomechanics, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
  • Zheng H; Paul C. Lauterbur Research Center for Biomedical Imaging, Institute of biomedical and Health Engineering, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
J Cell Mol Med ; 22(9): 4171-4182, 2018 09.
Article em En | MEDLINE | ID: mdl-29956460
ABSTRACT
The presence of blood-brain barrier (BBB) greatly limits the availability of drugs and their efficacy against glioma. Focused ultrasound (FUS) can induce transient and local BBB opening for enhanced drug delivery. Here, we developed polysorbate 80-modified paclitaxel-loaded PLGA nanoparticles (PS-80-PTX-NPs, PPNP) and examined the enhanced local delivery into the brain for glioma treatment by combining with FUS. Our result showed PPNP had good stability, fast drug release rate and significant toxicity to glioma cells. Combined with FUS, PPNP showed a stronger BBB permeation efficiency both in the in vitro and in vivo BBB models. Mechanism studies revealed the disrupted tight junction, reduced P-glycoprotein expression and ApoE-dependent PS-80 permeation collectively contribute to the enhanced drug delivery, resulting in significantly stronger antitumour efficacy and longer survival time in the tumour-bearing mice. Our study provided a new strategy to efficiently and locally deliver drugs into the brain to treat glioma.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polissorbatos / Neoplasias Encefálicas / Sistemas de Liberação de Medicamentos / Paclitaxel / Glioblastoma / Nanopartículas / Antineoplásicos Fitogênicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polissorbatos / Neoplasias Encefálicas / Sistemas de Liberação de Medicamentos / Paclitaxel / Glioblastoma / Nanopartículas / Antineoplásicos Fitogênicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article