Related Experiment Video
Updated: Jun 24, 2026

09:28
Engineering Molecular Recognition with Bio-mimetic Polymers on Single Walled Carbon Nanotubes
Published on: January 10, 2017
Long-term small molecule and protein elution from TiO2 nanotubes
Lily Peng1, Adam D Mendelsohn, Thomas J LaTempa
1Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, California 94158-2330, USA.
Nano Letters
|March 28, 2009
Summary
Titanium dioxide (TiO2) nanotubes effectively controlled the release of small molecule drugs and large proteins for weeks to a month. Eluted drugs maintained bioactivity, suggesting TiO2 nanotubes are promising for drug-eluting implant coatings.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Drug Delivery Systems
Background:
- Controlled drug release is crucial for implantable medical devices.
- Titanium dioxide (TiO2) nanotubes offer tunable properties for biomedical applications.
Purpose of the Study:
- To investigate the elution kinetics of small molecule drugs (sirolimus, paclitaxel) and a large protein (albumin) from TiO2 nanotubes.
- To assess the bioactivity of eluted drugs.
- To determine the potential of TiO2 nanotubes as a drug-eluting implant coating.
Main Methods:
- Fabrication of TiO2 nanotubes with varying dimensions.
- In vitro elution studies using albumin, sirolimus, and paclitaxel.
- Assessment of drug bioactivity through in vitro cell proliferation assays.
Main Results:
- TiO2 nanotubes demonstrated controlled release of small molecules for weeks and large molecules for up to a month.
- Eluted drugs retained bioactivity, inhibiting cell proliferation in vitro.
- Elution kinetics were significantly influenced by nanotube height.
Conclusions:
- TiO2 nanotubes provide a promising platform for controlled drug delivery.
- The dimensions of TiO2 nanotubes, particularly height, are critical for modulating elution profiles.
- These findings support the potential use of TiO2 nanotubes in developing advanced drug-eluting implant coatings.

