H NMR, FTIR and WXRD techniques. Its thermal and light responsive properties were demonstrated by turbidity measurements and UV spectroscopy, respectively. Furthermore, micelles with diameters of around 100 nm were prepared from APRTBP in aqueous solution. Dynamic laser scattering (DLS) measurements demonstrated that the micelles contracted under UV irradiation and successively expanded under visible light, which offers a reversible on-off switch for controlling the drug release behavior of micelles. Consequently, the in vitro drug release curve, which is similar to the pharmacokinetic curve of multiple dosing administrations, was achieved when UV and visible light were applied alternatively to simulate on-off states for drug release. It also showed that the micelle possessed a significantly higher release rate and higher cumulative release amount under UV irradiation than those under visible light. Furthermore, the low critical solution temperature (LCST) of NIPPAAm blocks in APRTBP can be used as another switch to trigger the drug release as implied by in vitro drug release tests using doxorubicin (DOX) as the model drug. Considering its interesting dual stimuli-responsiveness and on-off switch-like behaviors resulting from dual responsiveness, APRTBP shows considerable potential as a candidate for controlled drug delivery systems and other possible biomedical applications.
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Ye et al. (2014) studied this question.
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