Caon Thiago, Jin Liang, Simões Cláudia M O, Norton Raymond S, Nicolazzo Joseph A
Drug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, 381 Royal Parade, Parkville, VIC, 3052, Australia.
Pharm Res. 2015 Jan;32(1):1-21. doi: 10.1007/s11095-014-1485-1. Epub 2014 Aug 29.
With continuing advances in biotechnology and genetic engineering, there has been a dramatic increase in the availability of new biomacromolecules, such as peptides and proteins that have the potential to ameliorate the symptoms of many poorly-treated diseases. Although most of these macromolecular therapeutics exhibit high potency, their large molecular mass, susceptibility to enzymatic degradation, immunogenicity and tendency to undergo aggregation, adsorption, and denaturation have limited their ability to be administered via the traditional oral route. As a result, alternative noninvasive routes have been investigated for the systemic delivery of these macromolecules, one of which is the buccal mucosa. The buccal mucosa offers a number of advantages over the oral route, making it attractive for the delivery of peptides and proteins. However, the buccal mucosa still exhibits some permeability-limiting properties, and therefore various methods have been explored to enhance the delivery of macromolecules via this route, including the use of chemical penetration enhancers, physical methods, particulate systems and mucoadhesive formulations. The incorporation of anti-aggregating agents in buccal formulations also appears to show promise in other mucosal delivery systems, but has not yet been considered for buccal mucosal drug delivery. This review provides an update on recent approaches that have shown promise in enhancing the buccal mucosal transport of macromolecules, with a major focus on proteins and peptides.
随着生物技术和基因工程的不断进步,新的生物大分子,如具有改善许多治疗效果不佳疾病症状潜力的肽和蛋白质的可获得性显著增加。尽管这些大分子疗法大多显示出高效能,但其大分子质量、易受酶降解、免疫原性以及发生聚集、吸附和变性的倾向限制了它们通过传统口服途径给药的能力。因此,人们研究了替代的非侵入性途径用于这些大分子的全身递送,其中之一是颊黏膜。颊黏膜相对于口服途径具有许多优势,使其成为肽和蛋白质递送的有吸引力的途径。然而,颊黏膜仍然表现出一些限制通透性的特性,因此人们探索了各种方法来增强通过该途径的大分子递送,包括使用化学渗透促进剂、物理方法、微粒系统和黏膜黏附制剂。在颊制剂中加入抗聚集剂在其他黏膜递送系统中似乎也显示出前景,但尚未被考虑用于颊黏膜药物递送。本综述提供了关于最近在增强大分子颊黏膜转运方面显示出前景的方法的最新信息,主要关注蛋白质和肽。