In order to reduce the side effects of chemotherapy, target therapies have been spotlighted. In this study, paclitaxel, the drug for cancer treatment, is electrochemically deposited on Ti alloy as vascular stents for the tumor localized therapy by sustaining drug releasing to achieve the cancer cells apoptosis or the prevention of cancer metastasis. In the experiment, cathodic polarization tests coupled with electrochemical reactions were analyzed to speculate the deposition mechanism, and the field emission scanning electron microscope (FESEM), focused ion beam (FIB) system and Fourier transform infrared spectroscopy (FTIR) to observe the surface morphology and analyze constituent elements. A spectrophotometer (UV visible spectrometer) was used to measure drug loading and release. Finally, MTT Assay was carried out to analyze the cell viability for drug efficacy. It is concluded that paclitaxel can be successfully deposited on the titanium alloy by electrochemical method. Besides, the post-hydroxyapatite coated specimen with high porosity can enhance the drug loading from 395±95μg/cm2 to 572±99μg/cm2, a lower burst release in the first day, a higher sustaining release rate in a month, and the more complete drug release. All results indicate that the paclitaxel/hydroxyapatite composite coating by the electrochemical deposition method is much more effective and promising.
Keywords: Biomedical applications; Drug controlled release; Electrochemical deposition; Hydroxyapatite; Paclitaxel; Titanium alloy.
Copyright © 2017. Published by Elsevier B.V.