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Controlled Nutrient Delivery to Pancreatic Islets Using Polydopamine-Coated Mesoporous Silica Nanoparticles.
Razavi, Mehdi; Primavera, Rosita; Kevadiya, Bhavesh D; Wang, Jing; Ullah, Mujib; Buchwald, Peter; Thakor, Avnesh S.
Afiliação
  • Razavi M; Interventional Regenerative Medicine and Imaging Laboratory, Stanford University School of Medicine, Department of Radiology, Palo Alto, California 94304, United States.
  • Primavera R; Biionix (Bionic Materials, Implants & Interfaces) Cluster, Department of Internal Medicine, College of Medicine, University of Central Florida, Orlando, Florida 32827, United States.
  • Kevadiya BD; Department of Materials Science & Engineering, University of Central Florida, Orlando, Florida 32816, United States.
  • Wang J; Interventional Regenerative Medicine and Imaging Laboratory, Stanford University School of Medicine, Department of Radiology, Palo Alto, California 94304, United States.
  • Ullah M; Interventional Regenerative Medicine and Imaging Laboratory, Stanford University School of Medicine, Department of Radiology, Palo Alto, California 94304, United States.
  • Buchwald P; Interventional Regenerative Medicine and Imaging Laboratory, Stanford University School of Medicine, Department of Radiology, Palo Alto, California 94304, United States.
  • Thakor AS; Interventional Regenerative Medicine and Imaging Laboratory, Stanford University School of Medicine, Department of Radiology, Palo Alto, California 94304, United States.
Nano Lett ; 20(10): 7220-7229, 2020 10 14.
Article em En | MEDLINE | ID: mdl-32909757
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ilhotas Pancreáticas / Diabetes Mellitus Experimental / Nanopartículas Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ilhotas Pancreáticas / Diabetes Mellitus Experimental / Nanopartículas Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article