Department of Chemical Engineering and Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing Hua University, Hsinchu, 30013, Taiwan.
Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Zhunan, Miaoli, 35053, Taiwan.
Adv Mater. 2021 Aug;33(34):e2100701. doi: 10.1002/adma.202100701. Epub 2021 Jul 16.
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.
大多数口服药物由于肠上皮屏障(IEB)和血脑屏障(BBB)而无法到达脑内区域,这两个屏障位于肠道和大脑之间。在此,开发了一种口服前药传递系统,可无创地克服 IEB 和 BBB,用于治疗神经胶质瘤。该前药是通过使用含二硫键的连接子将抗癌药物连接到β-葡聚糖上制备的。在荷神经胶质瘤小鼠口服给药后,所制备的前药可以特异性靶向肠道 M 细胞,穿过 IEB,并被局部巨噬细胞(Mϕ)吞噬/搭便车。Mϕ 搭便车前药通过淋巴系统被转运到循环系统,穿过 BBB。然后,肿瘤过表达的谷胱甘肽在药物前体中切割二硫键,释放出活性药物,提高了治疗效果。这些发现表明,所开发的前药可作为一种从肠道到大脑的口服药物传递平台,用于神经胶质瘤的靶向治疗。