Banerjee Amrita, Lee JooHee, Mitragotri Samir
Dept. of Chemical Engineering University of California Santa Barbara Santa Barbara CA 93106.
Center for Bioengineering University of California Santa Barbara Santa Barbara California 93106.
Bioeng Transl Med. 2016 Aug 19;1(3):338-346. doi: 10.1002/btm2.10015. eCollection 2016 Sep.
Oral delivery of proteins such as insulin has been a long-lasting challenge owing to gastrointestinal degradation and poor permeability of therapeutic macromolecules across biological membranes. We have developed mucoadhesive intestinal devices for oral delivery of insulin to address this challenge. Here we demonstrate a combination of intestinal devices and a permeation enhancer, dimethyl palmitoyl ammonio propanesulfonate (PPS), for oral delivery of insulin. The devices were delivered from a capsule coated with a pH-responsive enteric coating. The devices adhere to intestinal mucosa, release their protein load unidirectionally, and prevent enzymatic degradation in the gut. Devices were found to completely release their drug load within 3-4 hr and showed excellent strength of mucoadhesion to porcine intestine. Devices loaded with insulin and PPS significantly decreased blood glucose levels by 30 and 33% in diabetic and nondiabetic rats, respectively. These studies demonstrate that intestinal mucoadhesive devices are a promising oral alternative to insulin injections and therefore should be further explored for the treatment of diabetes.
由于胃肠道的降解作用以及治疗性大分子跨生物膜的渗透性较差,口服递送胰岛素等蛋白质一直是一项长期挑战。我们开发了用于口服递送胰岛素的黏膜黏附性肠道装置,以应对这一挑战。在此,我们展示了一种肠道装置与渗透促进剂——二甲基棕榈酰氨丙基丙烷磺酸盐(PPS)相结合用于口服递送胰岛素的方法。这些装置由涂有pH响应性肠溶衣的胶囊递送。这些装置可黏附于肠黏膜,单向释放其负载的蛋白质,并防止在肠道内被酶降解。发现这些装置能在3 - 4小时内完全释放其药物负载,并对猪肠道显示出优异的黏膜黏附强度。装载有胰岛素和PPS的装置在糖尿病大鼠和非糖尿病大鼠中分别使血糖水平显著降低了30%和33%。这些研究表明,肠道黏膜黏附装置是胰岛素注射的一种有前景的口服替代方法,因此应进一步探索其在糖尿病治疗中的应用。