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Doxorubicin Adsorbed on Carbon Nanotubes: Helical Structure and New Release Trigger
Author(s) -
Sadaf Shamaila,
Walder Lorenz
Publication year - 2017
Publication title -
advanced materials interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.671
H-Index - 65
ISSN - 2196-7350
DOI - 10.1002/admi.201700649
Subject(s) - glutathione , carbon nanotube , intracellular , doxorubicin , materials science , biophysics , adsorption , extracellular , drug delivery , electrode , nanotechnology , chemical engineering , chemistry , organic chemistry , biochemistry , enzyme , chemotherapy , biology , genetics , engineering
The well‐known drug delivery system “doxorubicin physically loaded on carbon nanotubes” (Dox@CNT) is visualized by scanning tunneling microscopy at the molecular level, revealing rich architectural variability of Dox@CNT, and allowing to measure and rationalize reported loading efficiencies (80–200%) for the first time from image analysis. Reduction of Dox@CNT is identified as a so far unknown intrinsic release mechanism of biochemically relevance for Dox from Dox@CNT requiring no further CNT surface modification beside Dox loading. Electron injection into Dox@CNT from an electrode or from the biological reducing agent glutathione (GSH) leads to irreversible release of Dox. Its rate follows a linear free energy relationship (reduction potential vs log (Dox release rate)) with half‐life times from below seconds to hours. With extracellular GSH levels in the micromolar range and intracellular GSH concentrations of 10 × 10 −3 m or even higher, the findings can explain the preferential intracellular release of Dox from its physically adsorbed state on CNTs. The influence of acidity on the release rate of Dox on pristine 6,5‐CNTs in the absence of GSH is found to be negligible. The experimental findings are strongly supported by semi‐empirical calculations.