生物启发的正交形蛋白质生物金属纳米晶体可实现口服蛋白质吸收。

IF 10.5 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of Controlled Release Pub Date : 2024-11-13 DOI:10.1016/j.jconrel.2024.11.016
Matilde Durán-Lobato, Sulay Tovar, Juan Cuñarro, Rocío Ramos-Membrive, Iván Peñuelas, Ilaria Marigo, Federico Benetti, Miguel Chenlo, Clara V Álvarez, Vashegyi Ildikó, Rudolf Urbanics, János Szebeni, María José Alonso
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引用次数: 0

摘要

随着上市生物药物数量的不断增加,开发促进其口服全身吸收的技术策略变得越来越重要。恶劣的胃肠道环境和肠上皮的低通透性,对这些药物的全身给药构成了巨大挑战。本文从胰岛素与锌的生理性相互作用中汲取生物灵感,设计出了正交形状的蛋白质-生物金属杂化纳米晶体,并由双层功能性生物材料进一步包裹。这种纳米晶体的尺寸为 80 纳米,表面电荷为中性,胰岛素负载量高。体外研究表明,纳米复合物能够控制相关胰岛素的释放,同时保持其稳定性。体内评估显示,健康大鼠和糖尿病大鼠的血糖均有持续下降(分别高达 40% 和 80%),而小鼠的慢性免疫毒性研究则表明没有毒性影响。口服胶囊后对健康清醒猪进行的初步疗效研究显示,绝对生物利用率超过 20%。
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Bioinspired orthogonal-shaped protein-biometal nanocrystals enable oral protein absorption.

With the growing number of marketed biological drugs, the development of technological strategies for their oral systemic absorption, becomes increasingly important. The harsh gastrointestinal environment and low permeability of the intestinal epithelium, represent a huge challenge for their systemic delivery. Herein, bioinspired in the physiological insulin-Zn interaction, the design of orthogonal-shaped protein-biometal hybrid nanocrystals, further enveloped by a bilayer of functional biomaterials, is reported. The nanocrystals exhibited a size of 80 nm, a neutral surface charge and a high insulin loading. In vitro studies showed the capacity of the nanocomplexes to control the release of the associated insulin, while preserving its stability. In vivo evaluation showed sustained blood glucose reductions in both healthy and diabetic rats (up to 40 % and 80 %, respectively), while chronic immunotoxicity studies in mice indicated no toxicity effect. Preliminary efficacy studies in healthy awake pigs following oral capsule administration showed over 20 % absolute bioavailability.

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来源期刊
Journal of Controlled Release
Journal of Controlled Release 医学-化学综合
CiteScore
18.50
自引率
5.60%
发文量
700
审稿时长
39 days
期刊介绍: The Journal of Controlled Release (JCR) proudly serves as the Official Journal of the Controlled Release Society and the Japan Society of Drug Delivery System. Dedicated to the broad field of delivery science and technology, JCR publishes high-quality research articles covering drug delivery systems and all facets of formulations. This includes the physicochemical and biological properties of drugs, design and characterization of dosage forms, release mechanisms, in vivo testing, and formulation research and development across pharmaceutical, diagnostic, agricultural, environmental, cosmetic, and food industries. Priority is given to manuscripts that contribute to the fundamental understanding of principles or demonstrate the advantages of novel technologies in terms of safety and efficacy over current clinical standards. JCR strives to be a leading platform for advancements in delivery science and technology.
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