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提高口服治疗酶的稳定性和活性:最新进展和展望。

Improving the stability and activity of oral therapeutic enzymes-recent advances and perspectives.

机构信息

Institute of Pharmaceutical Sciences Department of Chemistry and Applied Biosciences, ETH Zurich, Wolfgang-Pauli-Str. 10, HCI H 301, 8093, Zurich, Switzerland.

出版信息

Pharm Res. 2014 May;31(5):1099-105. doi: 10.1007/s11095-013-1233-y. Epub 2013 Nov 2.

Abstract

Exogenous, orally-administered enzymes are currently in clinical use or under development for the treatment of pathologies, such as celiac disease and phenylketonuria. However, the administration of therapeutic enzymes via the oral route remains challenging due to potential inactivation of these fragile macromolecular entities in the harsh environment of the gastrointestinal tract. Enzymes are particularly sensitive because both proteolysis and unfolding can lead to their inactivation. Current efforts to overcome these shortcomings involve the application of gastro-resistant delivery systems and the modification of enzyme structures by polymer conjugation or protein engineering. This perspective manuscript reviews and critically discusses recent progress in the oral delivery of therapeutic enzymes, whose substrate is localized in the gastrointestinal tract.

摘要

外源性、口服给予的酶目前用于治疗某些疾病,例如乳糜泻和苯丙酮尿症,或正在开发中。然而,由于这些脆弱的大分子实体在胃肠道恶劣的环境中可能失活,通过口服途径给予治疗性酶仍然具有挑战性。酶特别敏感,因为蛋白水解和展开都可能导致其失活。目前克服这些缺点的努力包括应用胃耐型给药系统和通过聚合物缀合或蛋白质工程修饰酶结构。本文综述并批判性讨论了胃肠道局部定位的治疗性酶的口服递药的最新进展。

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