Multi-functional F127-grafted vitamin E succinate-modified liposomes for enhancing glioma therapy

In glioma treatment, the poor penetration of therapeutic drugs through the blood-brain barrier (BBB) to the tumor region, along with the intrinsic resistance of glioma cells <i>via</i> multiple survival mechanisms, remain major challenges. Liposomes are a popular choice for glioma therapy due to their ability to help drugs penetrate the BBB. However, unmodified liposomes have drawbacks, such as poor stability, low drug entrapment efficacy, and rapid removal from circulation, leading to reduced drug absorption at the lesion sites. To address these issues, a novel F127-grafted vitamin E succinate (F127-VES) was designed to prepare multifunctional modified liposomes for delivery of harmine (HAR). Compared to conventional liposomes (Ordinary-Lip), F127-VES-Lip shows greater potential in enhancing the anti-glioma effect of HAR. This is attributed to several key features: Firstly, Pluronic can enhance the transport across the blood-brain barrier. Secondly, the presence of F127 in the formulation extends the circulation time of the drug in the bloodstream. Finally, the combination of F127 and VES in F127-VES-Lip can induce tumor cell apoptosis. <i>In vitro</i> and <i>in vivo</i> results confirmed that the F127-VES-Lip could significantly elevate cellular uptake, promote apoptosis and increase the antitumor effect for C6 glioma cells. The F127-VES-Lip is a promising nanoformulation to enhance the effect of HAR for glioma treatment.

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Publication Details

Journal
Journal of Materials Chemistry B
Published
2025-01-01
DOI
https://doi.org/10.1039/d5tb01101a
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
Field-Weighted Citation Impact
0.00

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article

Multi-functional F127-grafted vitamin E succinate-modified liposomes for enhancing glioma therapy

Pengfei Yue, Yingchong Chen, Fang Li, Luqi Huang et al.
Journal of Materials Chemistry B
Nanoparticle-Based Drug Delivery
article

Multi-functional F127-grafted vitamin E succinate-modified liposomes for enhancing glioma therapy

Pengfei Yue, Yingchong Chen, Fang Li, Luqi Huang, Yuling Liu, Wenhui Hu, Haibin Zou
article en

Abstract

In glioma treatment, the poor penetration of therapeutic drugs through the blood-brain barrier (BBB) to the tumor region, along with the intrinsic resistance of glioma cells <i>via</i> multiple survival mechanisms, remain major challenges. Liposomes are a popular choice for glioma therapy due to their ability to help drugs penetrate the BBB. However, unmodified liposomes have drawbacks, such as poor stability, low drug entrapment efficacy, and rapid removal from circulation, leading to reduced drug absorption at the lesion sites. To address these issues, a novel F127-grafted vitamin E succinate (F127-VES) was designed to prepare multifunctional modified liposomes for delivery of harmine (HAR). Compared to conventional liposomes (Ordinary-Lip), F127-VES-Lip shows greater potential in enhancing the anti-glioma effect of HAR. This is attributed to several key features: Firstly, Pluronic can enhance the transport across the blood-brain barrier. Secondly, the presence of F127 in the formulation extends the circulation time of the drug in the bloodstream. Finally, the combination of F127 and VES in F127-VES-Lip can induce tumor cell apoptosis. <i>In vitro</i> and <i>in vivo</i> results confirmed that the F127-VES-Lip could significantly elevate cellular uptake, promote apoptosis and increase the antitumor effect for C6 glioma cells. The F127-VES-Lip is a promising nanoformulation to enhance the effect of HAR for glioma treatment.

Journal of Materials Chemistry BVol. 13(33)
Jiangxi University of Traditional Chinese Medicine (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
National Natural Science Foundation of China, Natural Science Foundation of Jiangxi Province
Good health and well-being
Openalex Percentile: Top 88%
Nanoparticle-Based Drug Delivery
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