Shaji Jessy, Patole V
Department of Pharmaceutical Sciences, Prin. K. M. Kundnani College of Pharmacy, Cuffe Parade, Mumbai-400 005, India.
Indian J Pharm Sci. 2008 May-Jun;70(3):269-77. doi: 10.4103/0250-474X.42967.
Till recent, injections remained the most common means for administering therapeutic proteins and peptides because of their poor oral bioavailability. However, oral route would be preferred to any other route because of its high levels of patient acceptance and long term compliance, which increases the therapeutic value of the drug. Designing and formulating a polypeptide drug delivery through the gastro intestinal tract has been a persistent challenge because of their unfavorable physicochemical properties, which includes enzymatic degradation, poor membrane permeability and large molecular size. The main challenge is to improve the oral bioavailability from less than 1% to at least 30-50%. Consequently, efforts have intensified over the past few decades, where every oral dosage form used for the conventional small molecule drugs has been used to explore oral protein and peptide delivery. Various strategies currently under investigation include chemical modification, formulation vehicles and use of enzyme inhibitors, absorption enhancers and mucoadhesive polymers. This review summarizes different pharmaceutical approaches which overcome various physiological barriers that help to improve oral bioavailability that ultimately achieve formulation goals for oral delivery.
直到最近,由于治疗性蛋白质和肽的口服生物利用度较差,注射仍然是给药的最常见方式。然而,由于患者接受度高且长期依从性好,口服途径比其他任何途径都更受青睐,这增加了药物的治疗价值。由于多肽具有不利的物理化学性质,包括酶降解、膜通透性差和分子量大,通过胃肠道设计和配制多肽药物递送系统一直是一项持续的挑战。主要挑战是将口服生物利用度从不到1%提高到至少30-50%。因此,在过去几十年里,人们加大了努力,使用了用于传统小分子药物的各种口服剂型来探索口服蛋白质和肽递送。目前正在研究的各种策略包括化学修饰、制剂载体以及使用酶抑制剂、吸收促进剂和粘膜粘附聚合物。本综述总结了不同的制药方法,这些方法克服了各种生理屏障,有助于提高口服生物利用度,最终实现口服递送的制剂目标。