纳米载体
离体
药物输送
体内
脂质体
药理学
化学
靶向给药
红细胞
医学
药品
体外
生物化学
生物
生物技术
有机化学
作者
Jacob S. Brenner,Daniel C. Pan,Jacob W. Myerson,Oscar A. Marcos‐Contreras,Carlos H. Villa,Priyal Patel,Hugh Hekierski,Shampa Chatterjee,Jian‐Qin Tao,Hamideh Parhiz,Kartik Bhamidipati,Thomas Uhler,Elizabeth D. Hood,Raisa Y. Kiseleva,Vladimir V. Shuvaev,Tea Shuvaeva,Makan Khoshnejad,Ian Johnston,Jason V. Gregory,Joerg Lahann
标识
DOI:10.1038/s41467-018-05079-7
摘要
Drug delivery by nanocarriers (NCs) has long been stymied by dominant liver uptake and limited target organ deposition, even when NCs are targeted using affinity moieties. Here we report a universal solution: red blood cell (RBC)-hitchhiking (RH), in which NCs adsorbed onto the RBCs transfer from RBCs to the first organ downstream of the intravascular injection. RH improves delivery for a wide range of NCs and even viral vectors. For example, RH injected intravenously increases liposome uptake in the first downstream organ, lungs, by ~40-fold compared with free NCs. Intra-carotid artery injection of RH NCs delivers >10% of the injected NC dose to the brain, ~10× higher than that achieved with affinity moieties. Further, RH works in mice, pigs, and ex vivo human lungs without causing RBC or end-organ toxicities. Thus, RH is a clinically translatable platform technology poised to augment drug delivery in acute lung disease, stroke, and several other diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI