Yamamoto Akira
Department of Biopharmaceutics, Kyoto Pharmaceutical University.
Yakugaku Zasshi. 2024;144(7):697-714. doi: 10.1248/yakushi.23-00199.
It is well known that the oral bioavailability of hydrophilic and macromolecular drugs is generally very poor due to their poor membrane permeability characteristics. Among these poorly absorbed drugs, peptide and protein drugs are typical poorly absorbed drugs which have low stability and poor permeability in the gastrointestinal tract. Consequently, the clinical administration of peptide and protein drugs is presently limited to administration by injection. However, such frequent administration subjects the patients to considerable pain, and there is also the possibility of the manifestation of serious side effects. Therefore, various approaches have been examined to overcome the poor absorption characteristics of these drugs. These approaches include (1) to use additives including absorption enhancers and protease inhibitors, (2) to modify the chemical structure of peptide and protein drugs, and (3) to apply dosage forms to these drugs, (4) to develop a novel administration method for these drugs that can serve as an alternative to oral and injection administration. We demonstrated that intestinal and transmucosal absorption of peptide and protein drugs could be improved by using these approaches. These approaches may give us useful basic information to improve the intestinal and transmucosal absorption of peptide and protein drugs.
众所周知,亲水性和大分子药物的口服生物利用度通常非常低,这是由于它们的膜通透性较差。在这些吸收不良的药物中,肽类和蛋白质药物是典型的吸收不良药物,它们在胃肠道中稳定性低且通透性差。因此,目前肽类和蛋白质药物的临床给药仅限于注射给药。然而,如此频繁的给药会给患者带来相当大的痛苦,并且也有可能出现严重的副作用。因此,人们已经研究了各种方法来克服这些药物吸收不良的特性。这些方法包括:(1)使用包括吸收促进剂和蛋白酶抑制剂在内的添加剂;(2)修饰肽类和蛋白质药物的化学结构;(3)将剂型应用于这些药物;(4)开发一种可替代口服和注射给药的新型给药方法。我们证明,通过使用这些方法可以提高肽类和蛋白质药物的肠道和跨粘膜吸收。这些方法可能会为我们提供有用的基础信息,以改善肽类和蛋白质药物的肠道和跨粘膜吸收。