a Biomaterial Research Center, School of Pharmaceutical Sciences , Southern Medical University , Guangzhou , China.
b Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences , Southern Medical University , Guangzhou , China.
J Microencapsul. 2019 Jan;36(1):96-107. doi: 10.1080/02652048.2019.1604846. Epub 2019 May 9.
Polyelectrolyte complexes (PEC) provide new opportunities for controlled release system of drugs, and have potentials to address challenges on the way to effective oral insulin delivery. Here, an innovative pH-sensitive PEC for insulin oral administration was developed, which was formed by self-assembly of two oppositely charged nanoparticles (chitosan-coated nanoparticles and alginate-coated nanoparticles) through electrostatic interaction via optimised double emulsion method. The encapsulation efficiency of insulin-loaded alginate-coated and chitosan-coated nanoparticles were 81.5 ± 7.4% and 55.2 ± 7.0%, respectively, and the particle size of these nanoparticles were in 200-300 nm range. The pH-dependent morphology of PEC was observed by transmission electron microscopy. The PEC exhibited insulin release profile triggered by pH and was non-cytotoxicity against Caco-2 cell. The insulin-loaded PEC could decrease blood glucose levels effectively and prolong insulin release after oral administration to diabetic rats. The results illustrated that the as-prepared PEC may be employed as a potential oral insulin delivery system.
聚电解质复合物(PEC)为药物控制释放系统提供了新的机会,并有可能解决有效口服胰岛素传递途径上的挑战。在这里,开发了一种用于胰岛素口服给药的创新 pH 敏感 PEC,它是通过优化的双重乳液法通过静电相互作用自组装而成的两种带相反电荷的纳米粒子(壳聚糖包覆的纳米粒子和藻酸盐包覆的纳米粒子)。载胰岛素的藻酸盐包覆和壳聚糖包覆纳米粒子的包封效率分别为 81.5±7.4%和 55.2±7.0%,这些纳米粒子的粒径在 200-300nm 范围内。通过透射电子显微镜观察了 PEC 的 pH 依赖性形态。PEC 表现出 pH 触发的胰岛素释放特性,并且对 Caco-2 细胞无细胞毒性。载胰岛素的 PEC 可有效降低糖尿病大鼠的血糖水平,并延长口服给药后的胰岛素释放。结果表明,所制备的 PEC 可用作潜在的口服胰岛素递送系统。