还原和温度双重敏感P(NIPAM-AA)纳米凝胶的合成及载药性能

Although doxorubicin(DOX) has been widely used in the treatment of different types of cancer, the multi-drug resistance is still a bottle for its further clinical applications. Nanogels with high loading capacity, good stability, environmental responsiveness(such as ionic strength, pH, temperature, reducing agent), are promising therapeutic nanocarriers for targeting delivery of drugs in a controllable way. In this study, a series of thermo- and redox-sensitive P(NIPAM-AA) nanogels was developed by free radical precipitation polymerization of N-isopropylacrylamide(NIPAM) and acrylic acid(AA) as monomers in the presence of N, N'-bis(acryloyl) cystamine(BAC) as crosslinking agent. The structures, particle size, Zeta potential, morphology, encapsulation efficiency and drug cumulative release [ using doxorubicin(DOX) as an anticancer model drug ] of the prepared composite nanogels were characterized by FTIR, Raman spectrum, dynamic light scattering(DLS), scanning electron microscopy(SEM) and ultraviolet-visible(UV-Vis) techniques. DLS study showed that BAC concentrations had great influence on thermo-sensitivity of nanogels as well as their Zeta potentials. UV-Vis study showed that when concentration of BAC was 1. 6 and 0. 32 mmol/L, nanogels had good drug encapsulation efficiency(64. 9% and 53. 5%, respectively). In vitro release study showed that temperature controlled DOX release was not obviously(DOX cumulative release at 4 h was 56% and 58% at 25 and 37 degrees C, respectively) for the 0. 32 mmol/L BAC-crosslinking system, probably because of the loose structure of the nanogels at low crosslinking degree that allows for rapid DOX diffusion from the nanogels at both temperatures. When BAC concentration was increased to 1. 6 mmol/L, DOX cumulative release at 4 h was 56% and 61% at 25 and 37 degrees C, respectively. The release rate can be further accelerated in a medium mimicking the intracellular reductive environment(37 degrees C and in the presence of 4 mmol/L D, L-dithiothreitol). The nanogels with good thermo- and redox-sensitivity can act as a good platform for delivery of various kinds of therapeutics, beyond anticancer drugs.