Department of Pharmaceutical Sciences, University of Calabria, Edificio Polifunzionale, Rende (CS), Italy.
Pharm Dev Technol. 2013 Sep-Oct;18(5):1026-34. doi: 10.3109/10837450.2011.644298. Epub 2011 Dec 27.
Thermo-responsive polysaccharidic hydrogels were designed and synthesized by a free radical induced grafting procedure. Chitosan was chosen as biopolymer to impart biocompatibility and biodegradability to the macromolecular systems, while N-isopropylacrylamide (NIPAAm) was selected as co-monomer responsive for the thermo-sensitive properties. Ammonium persulfate was the initiator system and different polymeric networks have been synthesized by modulating the amount of NIPAAm in the polymerization feed. The resulting hydrogels were proposed as drug delivery devices and their performance was evaluated by using Diclofenac sodium salt as a model drug. Hydrogels were carefully characterized by FT-IR spectrophotometry, calorimetric analyses and swelling behavior in a temperature range of 15-45°C. Finally, to verify the suitability of these hydrogels as thermo-responsive devices, the drug release profiles were studied performing in vitro experiments around the swelling-shrinking transition temperatures of the macromolecular systems.
通过自由基引发接枝法设计并合成了温敏多糖水凝胶。壳聚糖被选为生物聚合物,以使高分子体系具有生物相容性和可生物降解性,而 N-异丙基丙烯酰胺(NIPAAm)则被选为对温敏特性有响应的共聚单体。过硫酸铵是引发剂体系,通过调节聚合进料中 NIPAAm 的量合成了不同的聚合网络。所得到的水凝胶被提议作为药物输送装置,并通过使用双氯芬酸钠盐作为模型药物来评估其性能。通过傅里叶变换红外光谱、量热分析和在 15-45°C 的温度范围内的溶胀行为对水凝胶进行了仔细的表征。最后,为了验证这些水凝胶作为温敏装置的适用性,在高分子体系的溶胀-收缩转变温度周围进行了体外实验,研究了药物释放曲线。