Enzyme-activated intracellular drug delivery with tubule clay nanoformulation

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作者
Maria R. Dzamukova
Ekaterina A. Naumenko
Yuri M. Lvov
Rawil F. Fakhrullin
机构
[1] Bionanotechnology Lab,
[2] Institute of Fundamental Medicine and Biology,undefined
[3] Kazan Federal University,undefined
[4] Institute for Micromanufacturing,undefined
[5] Louisiana Tech University,undefined
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摘要
Fabrication of stimuli-triggered drug delivery vehicle s is an important milestone in treating cancer. Here we demonstrate the selective anticancer drug delivery into human cells with biocompatible 50-nm diameter halloysite nanotube carriers. Physically-adsorbed dextrin end stoppers secure the intercellular release of brilliant green. Drug-loaded nanotubes penetrate through the cellular membranes and their uptake efficiency depends on the cells growth rate. Intercellular glycosyl hydrolases-mediated decomposition of the dextrin tube-end stoppers triggers the release of the lumen-loaded brilliant green, which allowed for preferable elimination of human lung carcinoma cells (А549) as compared with hepatoma cells (Hep3b). The enzyme-activated intracellular delivery of brilliant green using dextrin-coated halloysite nanotubes is a promising platform for anticancer treatment.
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