期刊
MACROMOLECULAR RESEARCH
卷 30, 期 5, 页码 314-324出版社
POLYMER SOC KOREA
DOI: 10.1007/s13233-022-0035-7
关键词
cisplatin; drug delivery; hydrogel; PNIPAAm; RAFT polymerization; thermo-responsive polymers
资金
- Shiraz University Research Council
- Research Council of Shiraz University of Medical Sciences [98-01-36-21474/20221]
PNIPAAm hydrogel was synthesized using RAFT polymerization and modified with a pH-sensitive linker (spermine) to conjugate the anti-tumor drug, cisplatin. The drug release from this system showed temperature and pH-dependent behavior, with increased release at the polymer's transition temperature. In vitro toxicity assessment demonstrated the efficient killing of breast cancer cells.
Poly(N-isopropylacrylamide) (PNIPAAm) hydrogel as a temperature-responsive polymer was prepared through controlled process using reversible addition fragmentation chain transfer (RAFT) polymerization. The hydrogel was then amino modified using a biocompatible polyamine i.e. spermine and next the antitumor cisplatin drug was conjugated to the modified hydrogel via pH-sensitive spermine linkage. This system had a pH dependency and temperature sensitivity at lower critical solution temperature (LCST). Cisplatin potentially is liberated from the carrier in the acidic environment However, the release of cisplatin from this polymeric system is increased considerably around the transition temperature of the polymer. The drug release manner of the prepared hydrogel was determined at two pH values (5.5 and 7.4) and three temperatures (37, 40 and 42 degrees C) at different time intervals. The in vitro toxicity assessment was conducted on MCF-7 cell line which showed the system efficiency in killing breast cancer cells.
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