← 返回

Engineered Extracellular Vesicles As a New Delivery Platform for Migraine.

Engineered Extracellular Vesicles As a New Delivery Platform for Migraine.

期刊: ACS applied bio materials 日期: 2026-08-03 PMID: 42545034 DOI: 10.1021/acsabm.6c00833 浏览: 6
作者: Subramony A, Patel VK, Syam Kumar S, Nair SC
A, S., VK, P., S, S.K., & SC, N. (2026). Engineered Extracellular Vesicles As a New Delivery Platform for Migraine.. ACS applied bio materials. https://doi.org/10.1021/acsabm.6c00833
A S, VK P, S SK, SC N. Engineered Extracellular Vesicles As a New Delivery Platform for Migraine.. ACS applied bio materials. 2026; doi: 10.1021/acsabm.6c00833
A S, VK P, S SK, et al. Engineered Extracellular Vesicles As a New Delivery Platform for Migraine.[J]. ACS applied bio materials. 2026. DOI: 10.1021/acsabm.6c00833.
@article{a2026,
  author = {Subramony A and Patel VK and Syam Kumar S and Nair SC},
  title = {Engineered Extracellular Vesicles As a New Delivery Platform for Migraine.},
  journal = {ACS applied bio materials},
  year = {2026},
  doi = {10.1021/acsabm.6c00833},
  note = {PMID: 42545034},
}
TY  - JOUR
AU  - Subramony A
AU  - Patel VK
AU  - Syam Kumar S
AU  - Nair SC
TI  - Engineered Extracellular Vesicles As a New Delivery Platform for Migraine.
T2  - ACS applied bio materials
PY  - 2026
DO  - 10.1021/acsabm.6c00833
AN  - PMID:42545034
ER  - 

摘要

Migraine represents a complex neurovascular disorder that is challenging to treat due to the blood-brain barrier (BBB) and complex pathophysiology involving the trigeminovascular system, neuroinflammation, and cortical spreading depression. Current systemic therapies, including calcitonin gene-related peptide (CGRP) inhibitors, offer benefits but have limited efficacy and may cause adverse effects; thus, highlighting the need for targeted delivery across the BBB. This review introduces extracellular vesicles (EVs) as an appropriate pharmaceutical engineering platform to address such challenges. While traditional treatments have inherent disadvantages, engineered EVs offer efficient blood-brain barrier (BBB) penetration, targeted delivery, and multi-therapeutic payload capacity for migraine-associated neural circuits. We introduce a framework for pathophysiology-informed technology by first discussing the role of native EVs in promoting the migraine cascade to identify specific sites of therapeutic intervention. In this review, the focus is on pharmaceutical nanotechnology, starting with the strategic selection of producer cells, including "Hijack & Modify" vs De Novo Design, and continuing through sequential nano-engineering of EVs by surface functionalization and utilization of hybrid vesicles for targeting the BBB and trigeminovascular systems to state-of-the-art smart-release systems. We continue with the critical analytical and manufacturing sciences needed to translate such engineered EVs from bench to bedside, addressing important translational challenges through scalable Good manufacturing practices (GMP) production, supported potency assays, and comprehensive quality assurance processes. These include potency tests, GMP production, and robust quality control that may be expanded. Finally, we combine all of these into a single translational pathway that examines the regulatory issues, the patent landscape, and the future of personalized EV therapeutics. The current review provides an exhaustive framework for developing EV-based treatments by combining cutting-edge pharmaceutical nanotechnology with deep biological insights to make migraine treatment more reliable.

AI 智能解读

相关文献

返回分类: 心血管 查看原文 (DOI)
已选择 0 篇文献