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经鼻递送肽类药物的研发。

Drug development of intranasally delivered peptides.

作者信息

Campbell Catherine, Morimoto Bruce H, Nenciu Daniela, Fox Anthony W

机构信息

Allon Therapeutics Inc., 1168 Hamilton St, Vancouver, British Columbia, V6B 2S2, Canada.

出版信息

Ther Deliv. 2012 Apr;3(4):557-68. doi: 10.4155/tde.12.12.

Abstract

Intranasal drug delivery has attracted increasing attention as a noninvasive route of administration for therapeutic proteins and peptides. The delivery of therapeutic peptides through the nasal route provides an alternative to intravenous or subcutaneous injections. This review highlights the drug-development considerations unique to nasal therapeutics and discusses some of the factors and strategies that affect and can improve nasal absorption of peptides. The selectivity and good safety profile typical of peptide therapeutics, along with the dose limitation for intranasal administration, can provide challenges in drug development. Therefore, nasal peptide therapeutics often require special considerations in the nonclinical safety evaluations, such as determining drug exposure in the context of the maximum feasible dose in order to adequately prepare nasal products for clinical studies.

摘要

作为治疗性蛋白质和肽的一种非侵入性给药途径,鼻内给药越来越受到关注。通过鼻腔途径递送治疗性肽为静脉注射或皮下注射提供了一种替代方法。本综述重点介绍了鼻腔治疗药物特有的药物开发考虑因素,并讨论了一些影响和可改善肽类鼻腔吸收的因素及策略。肽类治疗药物典型的选择性和良好安全性,以及鼻内给药的剂量限制,可能会给药物开发带来挑战。因此,鼻腔肽类治疗药物在非临床安全性评估中通常需要特殊考虑,例如在最大可行剂量的背景下确定药物暴露量,以便为临床研究充分准备鼻腔产品。

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