Seyam Salma, Nordin Norsyafikah Asyilla, Alfatama Mulham
Faculty of Pharmacy, Universiti Sultan Zainal Abidin, Besut Campus, Besut 22200, Terengganu, Malaysia.
Pharmaceuticals (Basel). 2020 Oct 14;13(10):307. doi: 10.3390/ph13100307.
Diabetes mellitus is a chronic endocrine disease, affecting more than 400 million people around the world. Patients with poorly controlled blood glucose levels are liable to suffer from life-threatening complications, such as cardiovascular, neuropathy, retinopathy and even premature death. Today, subcutaneous parenteral is still the most common route for insulin therapy. Oral insulin administration is favourable and convenient to the patients. In contrast to injection route, oral insulin delivery mimics the physiological pathway of endogenous insulin secretion. However, oral insulin has poor bioavailability (less than 2%) due to the harsh physiological environment through the gastrointestinal tract (GIT). Over the last few decades, many attempts have been made to achieve an effective oral insulin formulation with high bioavailability using insulin encapsulation into nanoparticles as advanced technology. Various natural polymers have been employed to fabricate nanoparticles as a delivery vehicle for insulin oral administration. Chitosan, a natural polymer, is extensively studied due to the attractive properties, such as biodegradability, biocompatibility, bioactivity, nontoxicity and polycationic nature. Numerous studies were conducted to evaluate chitosan and chitosan derivatives-based nanoparticles capabilities for oral insulin delivery. This review highlights strategies that have been applied in the recent five years to fabricate chitosan/chitosan derivatives-based nanoparticles for oral insulin delivery. A summary of the barriers hurdle insulin absorption rendering its low bioavailability such as physical, chemical and enzymatic barriers are highlighted with an emphasis on the most common methods of chitosan nanoparticles preparation. Nanocarriers are able to improve the absorption of insulin through GIT, deliver insulin to the blood circulation and lower blood glucose levels. In spite of some drawbacks encountered in this technology, chitosan and chitosan derivatives-based nanoparticles are greatly promising entities for oral insulin delivery.
糖尿病是一种慢性内分泌疾病,全球有超过4亿人受其影响。血糖水平控制不佳的患者容易出现危及生命的并发症,如心血管疾病、神经病变、视网膜病变,甚至过早死亡。如今,皮下注射仍是胰岛素治疗最常见的途径。口服胰岛素对患者来说更有利且方便。与注射途径相比,口服胰岛素给药模拟了内源性胰岛素分泌的生理途径。然而,由于胃肠道(GIT)恶劣的生理环境,口服胰岛素的生物利用度很低(低于2%)。在过去几十年里,人们进行了许多尝试,采用将胰岛素封装到纳米颗粒中的先进技术来实现具有高生物利用度的有效口服胰岛素制剂。各种天然聚合物已被用于制备纳米颗粒,作为胰岛素口服给药的载体。壳聚糖是一种天然聚合物,因其具有诸如生物可降解性、生物相容性、生物活性、无毒性和聚阳离子性质等吸引人的特性而得到广泛研究。人们进行了大量研究来评估基于壳聚糖及其衍生物的纳米颗粒用于口服胰岛素给药的能力。本综述重点介绍了最近五年用于制备基于壳聚糖/壳聚糖衍生物的纳米颗粒以实现口服胰岛素给药的策略。总结了导致胰岛素吸收障碍及其低生物利用度的障碍,如物理、化学和酶促障碍,并重点介绍了壳聚糖纳米颗粒最常见的制备方法。纳米载体能够改善胰岛素通过胃肠道的吸收,将胰岛素输送到血液循环并降低血糖水平。尽管该技术存在一些缺点,但基于壳聚糖及其衍生物的纳米颗粒对于口服胰岛素给药来说是非常有前景的实体。