Blood triggered rapid release porous nanocapsules

纳米囊 药物输送 吲哚青绿 荧光 水溶液 控制释放 化学 纳米技术 聚合物 白蛋白 化学工程 材料科学 纳米颗粒 外科 有机化学 光学 医学 生物化学 物理 工程类
作者
Tiffany P. Gustafson,Sergey A. Dergunov,Walter J. Akers,Qian Cao,Selena Magalotti,Samuel Achilefu,Eugene Pinkhassik,М. Б. Березин
出处
期刊:RSC Advances [Royal Society of Chemistry]
卷期号:3 (16): 5547-5547 被引量:17
标识
DOI:10.1039/c3ra22693j
摘要

Rapid-release drug delivery systems present a new paradigm in emergency care treatments. Such systems combine a long shelf life with the ability to provide a significant dose of the drug to the bloodstream in the shortest period of time. Until now, development of delivery formulations has concentrated on slow release systems to ensure a steady concentration of the drug. To address the need for a quick release system, we created hollow polyacrylate nanocapsules with nanometer-thin porous walls. Burst release occurs upon interaction with blood components that leads to escape of the cargo. The likely mechanism of release involves a conformational change of the polymer shell caused by binding albumin. To demonstrate this concept, a near-infrared fluorescent dye indocyanine green (ICG) was incorporated inside the nanocapsules (NCs). ICG-loaded nanocapsules demonstrated a remarkable shelf life in aqueous buffers with no release of ICG for twelve months. Rapid release of the dye was demonstrated first in vitro using albumin solution and serum. SEM and light scattering analysis demonstrated the retention of the nanocapsule architecture after the release of the dye upon contact with albumin. In vivo studies using fluorescence lifetime imaging confirmed quick discharge of ICG from the nanocapsules following intravenous injection.

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