In this study, pH and thermally responsive P(PFPHM 9 -b-DMAEMA-b-PEG-MEA 480 ) was prepared by atom transfer radical polymerization (ATRP) using perfluoropolyether hydroxyethyl methacrylate (PFPHM) as hydrophobic core, 2-(Dimethylamino) ethyl methacrylate as pH and thermal response function segment, and poly (ethylene glycol) methyl ether acrylate 480 as hydrophilic shell, respectively. The chemical structure, critical micelle concentration (CMC), lower critical solution temperature (LCST), biological toxicity, stability of micelles, drug-loading performance and cumulative drug release rate of prepared P(PFPHM 9 -b-DMAEMA-b-PEGMEA 480 ) were analyzed by 19 F NMR, 1 H NMR, FTIR, DLS, UV-Vis, laser confocal microscopy and fluorescence spectrophotometer. The results show that P(PFPHM 9 -b-DMAEMA-b-PEGMEA 480 ) exhibites a CMC of 7.5 g/L, LCST of 37.6 C and excellent micelle stability.Moreover, the analysis of drug-loading indicates that the polymer displayed drug loading efficiency (DL) is 21.3% and the encapsulation efficiency (EE) is 90.0%. Its cumulative drug release rates at pH = 6.5 (42 C) is almost double of those at pH = 7.4 (42 C), pH = 6.5 (37 C) and pH = 7.4 (37 C). These results suggeste that the P(PFPHM 9 -b-DMAEMA-b-PEGMEA 480 ) at pH ranging from 6.5 to 7.4 and temperature ranging from 37 to 42 C are pH and temperature sensitive. It has great potential application as a drug loading for DOX.amphiphilicity, drug-loading, lower critical solution temperature, perfluoropolyether acyl fluoride, pH and thermal responsiveness
| INTRODUCTIONCancer has attracted widespread attention as one of the major threats to human health. Despite the significant progress made in current cancer treatment, a complete cure remains a thorny issue. 1 Chemotherapy is one of effective treatments for cancer, but the non-specific behavior of chemotherapy drugs can damage normal tissue cells, resulting in toxic side effects for patients. 2 Therefore, it is crucial to improve the utilization and selectivity of drugs on cancer cells. 3 Drug-loaded micelles formed by self-assembly of amphiphilic polymers as DDS have great potential for the treatment of cancer with good biocompatibility, high