Smart Surface-Engineered Mesoporous Silica Nanoparticles for Brain Tumor Therapy: Overcoming the Blood–Brain Barrier for Advanced Theranostics

IF 5.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Rachana SP, Rahul Pokale, Deepanjan Datta, Gaurisha alias Resha Ramnath Naik, Sandesh Ramchandra Jadhav, Ritu Kudarha, Srinivas Mutalik, Namdev Dhas
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Abstract

Brain tumors, particularly glioblastoma multiforme (GBM), remain among the most lethal forms of cancer due to their aggressive nature and the formidable challenge posed by the blood–brain barrier (BBB), which restricts the delivery of therapeutic agents. Conventional treatment modalities, including surgery, radiotherapy, and chemotherapy, often fail to achieve effective and targeted therapy without inducing systemic toxicity or damaging healthy brain tissue. In recent years, mesoporous silica nanoparticles (MSNs)have emerged as a versatile platform for targeted brain tumor therapy because of their high surface area, tunable pore structure, biocompatibility, and ease of surface functionalization. This review critically examines advanced surface functionalization strategies, including chemical functionalization (amine, thiol, carboxyl groups), ligand conjugation (antibodies, aptamers, peptides), and polymeric coatings (PEG, chitosan, PLGA) that enhance BBB penetration, facilitate tumor-specific targeting, and enable stimuli-responsive drug release (different types of exogenous and endogenous). We also explore the interactions of these modifications with key signaling pathways (e.g., Wnt/β-catenin, PDGF-B, TGF-β) that regulate BBB integrity and glioma progression. Special emphasis is placed on how surface-engineered MSNs can improve site-specific drug delivery, increase therapeutic accumulation in brain tumor tissue, and minimize off-target toxicity. Despite the considerable promise demonstrated by these techniques in preclinical glioma models, obstacles such as scalable synthesis, regulatory compliance, and long-term biosafety must be addressed to facilitate clinical translation. This review focuses specifically on brain tumor targeting via functionalized MSNs and provides mechanistic insights while highlighting emerging strategies to advance MSNs as next-generation therapeutics for brain tumor treatment.

Graphical Abstract

用于脑肿瘤治疗的智能表面工程介孔二氧化硅纳米颗粒:克服先进治疗的血脑屏障。
脑肿瘤,特别是多形性胶质母细胞瘤(GBM),由于其侵袭性和血脑屏障(BBB)带来的巨大挑战,限制了治疗药物的递送,仍然是最致命的癌症之一。传统的治疗方式,包括手术、放疗和化疗,往往无法在不引起全身毒性或损害健康脑组织的情况下实现有效和靶向治疗。近年来,介孔二氧化硅纳米颗粒(MSNs)因其高表面积、可调节的孔隙结构、生物相容性和易于表面功能化而成为靶向脑肿瘤治疗的多功能平台。本文综述了先进的表面功能化策略,包括化学功能化(胺、硫醇、羧基)、配体偶联(抗体、适体、肽)和聚合物涂层(聚乙二醇、壳聚糖、PLGA),它们可以增强血脑屏障的渗透,促进肿瘤特异性靶向,并促进刺激反应性药物释放(不同类型的外源性和内源性)。我们还探讨了这些修饰与调节血脑屏障完整性和胶质瘤进展的关键信号通路(如Wnt/β-catenin, PDGF-B, TGF-β)的相互作用。特别强调的是表面工程msn如何改善部位特异性药物递送,增加治疗在脑肿瘤组织中的积累,并最大限度地减少脱靶毒性。尽管这些技术在临床前胶质瘤模型中显示出相当大的前景,但必须解决诸如可扩展合成、法规遵从性和长期生物安全性等障碍,以促进临床转化。这篇综述特别关注了通过功能化的msn靶向脑肿瘤,并提供了机制见解,同时强调了推动msn作为下一代脑肿瘤治疗药物的新兴策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
AAPS PharmSciTech
AAPS PharmSciTech 医学-药学
CiteScore
6.80
自引率
3.00%
发文量
264
审稿时长
2.4 months
期刊介绍: AAPS PharmSciTech is a peer-reviewed, online-only journal committed to serving those pharmaceutical scientists and engineers interested in the research, development, and evaluation of pharmaceutical dosage forms and delivery systems, including drugs derived from biotechnology and the manufacturing science pertaining to the commercialization of such dosage forms. Because of its electronic nature, AAPS PharmSciTech aspires to utilize evolving electronic technology to enable faster and diverse mechanisms of information delivery to its readership. Submission of uninvited expert reviews and research articles are welcomed.
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