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一种口服葡萄糖响应性聚合物复合物,用于在小鼠和猪体内高效安全地递送胰岛素。

An orally administered glucose-responsive polymeric complex for high-efficiency and safe delivery of insulin in mice and pigs.

作者信息

Ji Kangfan, Wei Xiangqian, Kahkoska Anna R, Zhang Juan, Zhang Yang, Xu Jianchang, Wei Xinwei, Liu Wei, Wang Yanfang, Yao Yuejun, Huang Xuehui, Mei Shaoqian, Liu Yun, Wang Shiqi, Zhao Zhengjie, Lu Ziyi, You Jiahuan, Xu Guangzheng, Shen Youqing, Buse John B, Wang Jinqiang, Gu Zhen

机构信息

State Key Laboratory of Advanced Drug Delivery and Release Systems, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.

Jinhua Institute of Zhejiang University, Jinhua, China.

出版信息

Nat Nanotechnol. 2024 Dec;19(12):1880-1891. doi: 10.1038/s41565-024-01764-5. Epub 2024 Sep 2.

Abstract

Contrary to current insulin formulations, endogenous insulin has direct access to the portal vein, regulating glucose metabolism in the liver with minimal hypoglycaemia. Here we report the synthesis of an amphiphilic diblock copolymer comprising a glucose-responsive positively charged segment and polycarboxybetaine. The mixing of this polymer with insulin facilitates the formation of worm-like micelles, achieving highly efficient absorption by the gastrointestinal tract and the creation of a glucose-responsive reservoir in the liver. Under hyperglycaemic conditions, the polymer triggers a rapid release of insulin, establishing a portal-to-peripheral insulin gradient-similarly to endogenous insulin-for the safe regulation of blood glucose. This insulin formulation exhibits a dose-dependent blood-glucose-regulating effect in a streptozotocin-induced mouse model of type 1 diabetes and controls the blood glucose at normoglycaemia for one day in non-obese diabetic mice. In addition, the formulation demonstrates a blood-glucose-lowering effect for one day in a pig model of type 1 diabetes without observable hypoglycaemia, showing promise for the safe and effective management of type 1 diabetes.

摘要

与目前的胰岛素制剂不同,内源性胰岛素可直接进入门静脉,以最小的低血糖风险调节肝脏中的葡萄糖代谢。在此,我们报告了一种两亲性二嵌段共聚物的合成,该共聚物由葡萄糖响应性带正电的链段和聚羧基甜菜碱组成。这种聚合物与胰岛素混合有助于形成蠕虫状胶束,实现胃肠道的高效吸收,并在肝脏中形成葡萄糖响应性储库。在高血糖条件下,该聚合物触发胰岛素的快速释放,建立门静脉到外周的胰岛素梯度,类似于内源性胰岛素,以安全调节血糖。这种胰岛素制剂在链脲佐菌素诱导的1型糖尿病小鼠模型中表现出剂量依赖性的血糖调节作用,并在非肥胖糖尿病小鼠中将血糖控制在正常血糖水平一天。此外,该制剂在1型糖尿病猪模型中显示出一天的降血糖作用,且无明显低血糖,显示出安全有效管理1型糖尿病的潜力。

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