前药
药理学
血脑屏障
医学
药品
药物输送
胶质瘤
中枢神经系统
癌症研究
材料科学
内科学
纳米技术
作者
Yang‐Bao Miao,Kuan‐Hung Chen,Chiung‐Tong Chen,Fwu‐Long Mi,Yu‐Jung Lin,Yen Chang,Chi‐Shiun Chiang,Jui‐To Wang,Kun‐Ju Lin,Hsing‐Wen Sung
标识
DOI:10.1002/adma.202100701
摘要
Most orally administered drugs fail to reach the intracerebral regions because of the intestinal epithelial barrier (IEB) and the blood-brain barrier (BBB), which are located between the gut and the brain. Herein, an oral prodrug delivery system that can overcome both the IEB and the BBB noninvasively is developed for treating gliomas. The prodrug is prepared by conjugating an anticancer drug on β-glucans using a disulfide-containing linker. Following oral administration in glioma-bearing mice, the as-prepared prodrug can specifically target intestinal M cells, transpass the IEB, and be phagocytosed/hitchhiked by local macrophages (Mϕ). The Mϕ-hitchhiked prodrug is transported to the circulatory system via the lymphatic system, crossing the BBB. The tumor-overexpressed glutathione then cleaves the disulfide bond within the prodrug, releasing the active drug, improving its therapeutic efficacy. These findings reveal that the developed prodrug may serve as a gut-to-brain oral drug delivery platform for the well-targeted treatment of gliomas.
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