Abstract

AbstractHomopolypeptide bearing azobenzene and triethylene glycol spacers, and 1‐butylimidazolium pendants, namely P(Azo‐OEG3‐ImX) (X = Cl, I, BF4) are prepared by 1,3‐dipolar cycloaddition and subsequent ion‐exchange reaction. Both 1H NMR and FTIR confirm the polymer structures and reveal a high grafting efficiency (97%). P(Azo‐OEG3‐ImI) shows reversible upper critical solution temperature (UCST)‐type thermoresponsive property in ethanol while P(Azo‐OEG3‐ImI/BF4) shows a UCST in ethanol/water solvent mixtures. P(Azo‐OEG3‐ImI) shows UCST‐type phase transitions in ethanol or ethanol/water solvent mixtures. After UV irradiation, the UCST‐type cloud point temperature (Tcp) remains constant in ethanol. However, it decreases after UV irradiation and increases after visible light irradiation in ethanol/water solvent mixtures due to the trans–cis isomerization of azobenzene moieties. P(Azo‐OEG3‐ImCl/I) shows NaI‐induced UCST in water. The Tcp of the P(Azo‐OEG3‐ImCl/I) aqueous solution is highly related to the polymer/salt concentration and nature of counteranions. P(Azo‐OEG3‐ImCl) also shows reversible light‐responsive properties in NaI aqueous solutions. Higher NaI concentration is needed to induce a UCST for P(Azo‐OEG3‐ImCl) after UV irradiation. Moreover, ciprofloxacin‐loaded hydrogel containing P(Azo‐OEG3‐ImCl) shows more efficient drug release while the UV irradiation leads to slightly low drug release.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call