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肽搭乘用于神经胶质瘤中纳米系统的发展。

Peptide-Hitchhiking for the Development of Nanosystems in Glioblastoma.

机构信息

Faculty of Pharmacy, University of Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, Portugal.

Coimbra Chemistry Centre, Institute of Molecular Sciences - IMS, Faculty of Sciences and Technology, University of Coimbra, 3004-535 Coimbra, Portugal.

出版信息

ACS Nano. 2024 Jul 2;18(26):16359-16394. doi: 10.1021/acsnano.4c01790. Epub 2024 Jun 11.


DOI:10.1021/acsnano.4c01790
PMID:38861272
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11223498/
Abstract

Glioblastoma (GBM) remains the epitome of aggressiveness and lethality in the spectrum of brain tumors, primarily due to the blood-brain barrier (BBB) that hinders effective treatment delivery, tumor heterogeneity, and the presence of treatment-resistant stem cells that contribute to tumor recurrence. Nanoparticles (NPs) have been used to overcome these obstacles by attaching targeting ligands to enhance therapeutic efficacy. Among these ligands, peptides stand out due to their ease of synthesis and high selectivity. This article aims to review single and multiligand strategies critically. In addition, it highlights other strategies that integrate the effects of external stimuli, biomimetic approaches, and chemical approaches as nanocatalytic medicine, revealing their significant potential in treating GBM with peptide-functionalized NPs. Alternative routes of parenteral administration, specifically nose-to-brain delivery and local treatment within the resected tumor cavity, are also discussed. Finally, an overview of the significant obstacles and potential strategies to overcome them are discussed to provide a perspective on this promising field of GBM therapy.

摘要

胶质母细胞瘤(GBM)仍然是脑瘤谱中侵袭性和致命性的代表,主要是由于血脑屏障(BBB)阻碍了有效治疗药物的递送、肿瘤异质性和存在治疗抵抗的干细胞,这些都导致肿瘤复发。纳米颗粒(NPs)通过附着靶向配体来提高治疗效果,从而克服了这些障碍。在这些配体中,肽因其易于合成和高选择性而脱颖而出。本文旨在对单配体和多配体策略进行批判性地综述。此外,它还强调了其他策略,这些策略整合了外部刺激、仿生方法和化学方法的影响,作为纳米催化药物,揭示了它们在使用肽功能化 NPs 治疗 GBM 方面的巨大潜力。还讨论了其他给药途径,特别是经鼻脑递药和在切除的肿瘤腔内进行局部治疗。最后,概述了克服这些重大障碍的潜在策略,为 GBM 治疗这一充满希望的领域提供了一个视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/db33b7d897d2/nn4c01790_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/a9f6063ee9ad/nn4c01790_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/e4e126268b6a/nn4c01790_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/5b60d7844e93/nn4c01790_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/c52ff95c114e/nn4c01790_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/0e6b196a6ac4/nn4c01790_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/2feb8250dab4/nn4c01790_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/db33b7d897d2/nn4c01790_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/a9f6063ee9ad/nn4c01790_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/e4e126268b6a/nn4c01790_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/5b60d7844e93/nn4c01790_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/c52ff95c114e/nn4c01790_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/0e6b196a6ac4/nn4c01790_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/2feb8250dab4/nn4c01790_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/497a/11223498/db33b7d897d2/nn4c01790_0007.jpg

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引用本文的文献

[1]
Better together: biomimetic nanomedicines for high performance tumor therapy.

Beilstein J Nanotechnol. 2025-8-5

[2]
Peptide-Based Nanoparticle for Tumor Therapy.

Biomedicines. 2025-6-9

[3]
Navigating the brain: Harnessing endogenous cellular hitchhiking for targeting neoplastic and neuroinflammatory diseases.

Asian J Pharm Sci. 2025-4

[4]
Precision-Guided Stealth Missiles in Biomedicine: Biological Carrier-Mediated Nanomedicine Hitchhiking Strategy.

Adv Sci (Weinh). 2025-6

[5]
Exosomes in the Chemoresistance of Glioma: Key Point in Chemoresistance.

J Cell Mol Med. 2025-2

[6]
Recent Treatment Strategies and Molecular Pathways in Resistance Mechanisms of Antiangiogenic Therapies in Glioblastoma.

Cancers (Basel). 2024-8-27

本文引用的文献

[1]
Targeted Glioma Therapy-Clinical Trials and Future Directions.

Pharmaceutics. 2024-1-11

[2]
In situ cellular hitchhiking of nanoparticles for drug delivery.

Adv Drug Deliv Rev. 2024-1

[3]
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Brain Sci. 2023-10-31

[4]
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J Control Release. 2024-1

[5]
Sonocatalytic cancer therapy: theories, advanced catalysts and system design.

Nanoscale. 2023-12-14

[6]
Improve BBB Penetration and Cytotoxicity of Palbociclib in U87-MG Glioblastoma Cells Delivered by Dual Peptide Functionalized Nanoparticles.

Pharmaceutics. 2023-10-6

[7]
Using Biosensors to Study Organoids, Spheroids and Organs-on-a-Chip: A Mechanobiology Perspective.

Biosensors (Basel). 2023-9-24

[8]
Ginsenoside Rg3 endows liposomes with prolonged blood circulation and reduced accelerated blood clearance.

J Control Release. 2023-12

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J Nanobiotechnology. 2023-10-14

[10]
Protein corona on brain targeted nanocarriers: Challenges and prospects.

Adv Drug Deliv Rev. 2023-11

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