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Fabrication of Quaternized Chitosan Nanoparticles Using Tripolyphosphate/Genipin Dual Cross-Linkers as a Protein Delivery System

机译:季铵化壳聚糖纳米粒子的使用三聚磷酸酯/ Genipin双交联剂作为蛋白质传递系统的制造。

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摘要

Various amounts of 2-((acryloyloxy)ethyl)trimethylammonium chloride were grafted onto chitosan (CS) via redox polymerization method to obtain water-soluble quaternized CS (QCS). The QCS nanoparticles loaded with bovine serum albumin (BSA) were then produced by ionic gelation with tripolyphosphate (TPP) and further covalently cross-linked with genipin. The formation of QCS nanoparticles was optimized as a function of monomer grafting yield, QCS/TPP weight ratio, and QCS/genipin weight ratio by Box-Behnken design and response surface methodology. The results showed that QCS nanoparticles prepared with a grafting yield of 50%, QCS/TPP weight ratio of 7.67, and QCS/genipin weight ratio of 60 had a particle size of 193.68 ± 44.92 nm, polydispersity of 0.232, zeta potential of +23.97 mV and BSA encapsulation efficiency of 46.37 ± 2.89%, which were close to the predicted values from mathematical models. In vitro drug release studies at pH 1.2 and pH 7.4 exhibited that the release rate of BSA was significantly decreased and the release period was significantly prolonged after QCS nanoparticles cross-linking with genipin. Therefore, QCS nanoparticles cross-linked with TPP/genipin dual cross-linkers may be a promising protein drug carrier for a prolonged and sustained delivery.
机译:通过氧化还原聚合法将各种量的2-((丙烯酰氧基)乙基)三甲基氯化铵接枝到壳聚糖(CS)上,得到水溶性季铵化CS(QCS)。然后,通过用三聚磷酸酯(TPP)进行离子凝胶化,然后再用京尼平进行共价交联,制得了装载牛血清白蛋白(BSA)的QCS纳米颗粒。通过Box-Behnken设计和响应面方法,优化了QCS纳米颗粒的形成与单体接枝产率,QCS / TPP重量比和QCS / genipin重量比的关系。结果表明,以接枝率为50%,QCS / TPP重量比为7.67和QCS / genipin重量比为60制备的QCS纳米粒子的粒径为193.68±44.92 nm,多分散度为0.232,ζ电位为+23.97。 mV和BSA的封装效率为46.37±2.89%,接近数学模型的预测值。在pH 1.2和pH 7.4下进行的体外药物释放研究表明,QCS纳米颗粒与genipin交联后,BSA的释放速率显着降低,释放时间显着延长。因此,与TPP / genipin双交联剂交联的QCS纳米粒子可能是有希望的蛋白质药物载体,可以延长和持续递送。

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