通过口服可摄取的机器人药丸经肠输送抗体,其生物利用度与清醒犬的肠外给药相当

Alyson Yamaguchi, J. van Dam, A. Dhalla, Kyle P. Horlen, M. Imran, April T. Vo, Mir Hashim
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引用次数: 0

摘要

多肽和抗体等生物治疗药物在临床上非常有效,但与传统药物不同的是,它们会被消化和失活,不能口服。因此,生物治疗药物需要通过静脉注射、肌肉注射或皮下注射等非肠外途径给药。然而,与口服治疗相比,这些给药方法有局限性,如患者依从性差或可能需要临床监督。我们探索了一种新的口服经肠给药系统(机器人药丸)是否能提供与非肠外给药相同的生物利用度。利用清醒犬模型,我们证明了口服含有人IgG或针对TNFα或白细胞介素- 17a的抗细胞因子单克隆抗体的机器人药丸产生的生物利用度与肠外给药的对照组相当。通过任何口服制剂达到临床相关的生物治疗药物血液水平的能力代表了药物传递的重要进步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transenteric delivery of antibodies via an orally ingestible robotic pill yields high bioavailability comparable to parenteral administration in awake canines
Biotherapeutics such as peptides and antibodies are highly efficacious clinically but, unlike conventional medications, cannot be administered orally as they get digested and inactivated. Thus, biotherapeutics require parenteral routes for delivery, such as intravenous, intramuscular or subcutaneous administration. However, these delivery methods have limitations such as poor patient compliance or may require clinical supervision compared to oral therapies. We explored whether a novel, orally administered transenteric delivery system (Robotic Pill) could provide equivalent bioavailability to parenterally administered drugs. Utilizing an awake canine model, we demonstrated that orally administered Robotic Pills containing either human IgG or an anti-cytokine monoclonal antibody directed against either TNFα or interleukin-17A yielded bioavailability equivalent to parenterally administered controls. The ability to achieve clinically relevant blood levels of biotherapeutics via any orally administered preparation represents an important advance in drug delivery.
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