膦酸盐
内吞作用
化学
药物输送
小分子
前药
生物物理学
胞饮病
膜
细胞内
分子
药品
纳米技术
组合化学
受体
生物化学
材料科学
药理学
生物
有机化学
作者
Biao Wu,Qingling Nie,Juan Tang,Yongsheng Li,Ji Wang,Boyang Li,Hongwei Ma,Xiao‐Juan Yang,Wei Zhao
标识
DOI:10.1002/anie.202509002
摘要
Phosphate/phosphonate‐based drugs (PDs), as multi‐negative, hydrophilic molecules, face the greatest difficulty in diffusion across biological membranes, leading to poor bioavailability. Conventional drug delivery strategies to overcome this issue, including utilizing small‐molecule prodrugs or nanoparticle carriers, often suffer from case‐specific modifications or uncertainties in drug loading. Inspired by the anion coordination chemistry of natural phosphate transporters and artificial anion receptors, here we present the first use of a neutral anion receptor, i.e., bis(tripodal hexaurea) cage 1, as a “single‐molecule carrier” for the delivery of PDs into living cells. Cage 1 features advantages of molecular‐level encapsulation, enhanced intracellular accumulation, subcellular targeting, responsive drug release, and broad adaptability. It enhances PD accumulation in tumor cells both in vitro and in vivo, enhancing the cellular uptake of mono‐, di‐, and tri‐phosphate/phosphonate substrates by up to 45‐fold via a macropinocytosis‐mediated endocytosis pathway. This work demonstrates the potential of neutral anion receptors to serve as single‐molecule carriers and offers a promising solution for improving PDs bioavailability, advancing the development of antitumor phosphate‐based drugs.
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