Biomaterials · 2026
Polyphosphorylcholine-modified liposomes for glioblastoma-targeted siRNA delivery across the blood-brain barrier.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Ismail Muhammad, Wang Ningyang, Li Yundong, Li Yanfei, Yang Qingshan, Zou Yan, Qin Changjiang, Zheng Meng, Shi Bingyang
Аннотация
Liposomes represent versatile drug delivery shuttles in clinics for cancer therapy. Nevertheless, traditional PEG-modified liposomes encounter difficulties, including (1) poor blood-brain barrier (BBB) transcytosis and tumor targeting without ligand-decoration; (2) accelerated blood clearance (ABC) resulting from anti-PEG antibodies and complement proteins. To overcome these challenges, we employed a ligand-free, BBB-permeable, and glioblastoma (GBM)-targeting zwitterionic polyphosphorylcholine (PMPC)-modified liposomal formulation for siRNA delivery (PMPC-Lipo@siRNA). PMPC-modified formulation leverages interactions with nicotinic acetylcholine receptors (nAChRs) and choline transporters (ChTs) to achieve effective BBB transcytosis and targeted tumor accumulation. Unlike anti-PEG antibodies-induced immunogenicity, PMPC modification successfully circumvents opsonin recognition, which potentially translates into their extended blood circulation and improved therapeutic responses. By targeting the PLK1 oncogene, PMPC-Lipo@siPLK1 effectively induced apoptosis through PLK1 inhibition, significantly extending the median survival of mice in both orthotopic human U87MG and patient-derived CSC2 stem cell xenograft models. Overall, PMPC-modified liposomes provide an effective ligand-free platform for GBM-targeted siRNA delivery by combining prolonged systemic circulation with intrinsic brain-targeting capability, highlighting their potential for RNAi-based therapy against GBM.