De novo fabrication of oral insulin-loaded chitosan/dextrin/pectin nanospheres and their antidiabetic efficacy in streptozotocin-induced diabetic rats

IF 0.9 Q4 MATERIALS SCIENCE, MULTIDISCIPLINARY
S. R. Mohammed, A. Abdel-Moneim, E. S. Abdel-Reheim, H. Ramadan, Z. E. Eldin, A. El-Shahawy, A. I. Yousef
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Abstract

Nanotechnology can offer various non-invasive and efficient alternative delivery strategies for insulin injections to enhance the quality of life of diabetic patients. The current research was aimed to fabricate a de novo oral formula of insulin-loaded chitosan nanoparticles coated with dextrin and pectin (INS-CN/DP) to improve the bioavailability and therapeutic efficiency of oral insulin. INS-CN/DP nano-formula was prepared using ionic gelation technique and characterized by XRD, FTIR, SEM, EDX, and DLS. Insulin loading capacity and entrapment efficiency (LC%, EE%), release profile, and kinetic study was conducted for INS-CN/DP nano-formula. Next, hypoglycemic and antidiabetic efficiency of INS-CN/DP nano-formula were studied in streptozotocin-induced diabetic rats by measuring fasting and postprandial glucose, the activities of carbohydrate metabolizing enzymes, liver glycogen content, and gene expression levels of glucokinase and Glucose transporter-2. Characterization results confirmed the formation of INSCN/DP nanoparticles with LC% =26.2 ± 0.56 and EE% 69.3 ± 2.75, respectively. Size average was 282.8 nm and nearly 25% of loaded insulin released after 4 hrs vs 48% for unloaded insulin. In vivo results displayed that oral administration of INS-CN/DP nanoparticles showed highly significant hypoglycemic and antidiabetic efficacy in diabetic rats compared to unloaded oral insulin. Oral INS-CN/DP nano-formula is promising alternative for insulin injections and can be suggested as non-invasive and effective diabetes therapy
壳聚糖/糊精/pectin纳米球的全新口服胰岛素载体制备及其在链脲佐菌素诱导的糖尿病大鼠中的抗糖尿病疗效
纳米技术可以为胰岛素注射提供各种非侵入性和高效的替代给药策略,从而提高糖尿病患者的生活质量。目前的研究旨在制备一种新的胰岛素负载壳聚糖纳米颗粒(INS-CN/DP),该纳米颗粒涂覆有糊精和果胶,以提高口服胰岛素的生物利用度和治疗效率。INS-CN/DP 纳米配方采用离子凝胶技术制备,并通过 XRD、FTIR、SEM、EDX 和 DLS 进行表征。对 INS-CN/DP 纳米制剂进行了胰岛素负载能力和夹带效率(LC%、EE%)、释放曲线和动力学研究。接着,通过测定空腹和餐后血糖、碳水化合物代谢酶的活性、肝糖原含量以及葡萄糖激酶和葡萄糖转运体-2的基因表达水平,研究了INS-CN/DP纳米配方在链脲佐菌素诱导的糖尿病大鼠中的降血糖和抗糖尿病效果。表征结果证实了 INSCN/DP 纳米粒子的形成,其 LC% =26.2 ± 0.56 和 EE% 69.3 ± 2.75。平均粒径为 282.8 纳米,4 小时后近 25% 的负载胰岛素释放出来,而未负载胰岛素的释放率为 48%。体内试验结果表明,与未载入的口服胰岛素相比,口服 INS-CN/DP 纳米颗粒对糖尿病大鼠具有非常显著的降血糖和抗糖尿病疗效。口服 INS-CN/DP 纳米配方有望替代胰岛素注射,可作为无创、有效的糖尿病疗法。
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来源期刊
Journal of Optoelectronic and Biomedical Materials
Journal of Optoelectronic and Biomedical Materials MATERIALS SCIENCE, MULTIDISCIPLINARY-
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