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使用聚多巴胺包覆的介孔硅纳米粒子实现对胰岛的受控营养物质输送。

Controlled Nutrient Delivery to Pancreatic Islets Using Polydopamine-Coated Mesoporous Silica Nanoparticles.

机构信息

Interventional Regenerative Medicine and Imaging Laboratory, Stanford University School of Medicine, Department of Radiology, Palo Alto, California 94304, United States.

Biionix (Bionic Materials, Implants & Interfaces) Cluster, Department of Internal Medicine, College of Medicine, University of Central Florida, Orlando, Florida 32827, United States.

出版信息

Nano Lett. 2020 Oct 14;20(10):7220-7229. doi: 10.1021/acs.nanolett.0c02576. Epub 2020 Sep 21.

Abstract

In the present study, we created a nanoscale platform that can deliver nutrients to pancreatic islets in a controlled manner. Our platform consists of a mesoporous silica nanoparticle (MSNP), which can be loaded with glutamine (G: an essential amino acid required for islet survival and function). To control the release of G, MSNPs were coated with a polydopamine (PD) layer. With the optimal parameters (0.5 mg/mL and 0.5 h), MSNPs were coated with a layer of PD, which resulted in a delay of G release from MSNPs over 14 d (57.4 ± 4.7% release). Following syngeneic renal subcapsule islet transplantation in diabetic mice, PDG-MSNPs improved the engraftment of islets (i.e., enhanced revascularization and reduced inflammation) as well as their function, resulting in re-establishment of glycemic control. Collectively, our data show that PDG-MSNPs can support transplanted islets by providing them with a controlled and sustained supply of nutrients.

摘要

在本研究中,我们创建了一个纳米级平台,能够以可控的方式将营养物质递送到胰岛。我们的平台由介孔硅纳米颗粒(MSNP)组成,它可以负载谷氨酰胺(G:胰岛存活和功能所必需的必需氨基酸)。为了控制 G 的释放,MSNPs 被包裹上聚多巴胺(PD)层。在最佳参数(0.5mg/mL 和 0.5h)下,MSNPs 被包裹上 PD 层,导致 G 从 MSNPs 中的释放延迟超过 14 天(57.4±4.7%的释放)。在糖尿病小鼠的同基因肾被膜下胰岛移植后,PDG-MSNPs 改善了胰岛的移植效果(即,增强了再血管化和减少了炎症)及其功能,从而重新建立了血糖控制。总的来说,我们的数据表明,PDG-MSNPs 可以通过为移植的胰岛提供受控和持续的营养物质供应来支持它们。

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