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

In this study, we designed a nanoscale platform for sustained amino acid delivery to support transplanted pancreatic islets. The platform features mesoporous silica nanoparticles (MSNPs) loaded with glutamine (G), an essential amino acid required for islet survival and function, and coated with polydopamine (PD). We investigated various PD concentrations (0.5-2 mg/mL) and incubation times (0.5-2 h) to optimize G release, identifying that a PD concentration of 0.5 mg/mL incubated for 0.5 h yielded the best results to support islet viability and functionality <i>ex vivo</i>, particularly under inflammatory conditions. In syngeneic islet transplantation in STZ-diabetic mice, G alone provided only temporary benefits; however, PD-G-MSNPs significantly improved islet engraftment and function, with animals maintaining glycemic control for 30 days due to controlled G release. Our findings support the use of this nanoscale platform to provide essential nutrients like G to transplanted islets until they can establish their own blood and nutrient supply.

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Publication Details

Journal
Nano Letters
Published
2025-01-10
DOI
https://doi.org/10.1021/acs.nanolett.4c03613
Citations
5
Primary Topic
Pancreatic function and diabetes
Type
article
Field-Weighted Citation Impact
10.03

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article

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

Péter Buchwald, Abantika Ganguly, Shashank Chetty, Steven Levitte et al.
5 citations
Nano Letters
Pancreatic function and diabetes
10.03
article

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

Péter Buchwald, Abantika Ganguly, Shashank Chetty, Steven Levitte, Rosita Primavera, Paolo Decuzzi, Bhavesh D. Kevadiya, Michele Guindani, Reza Yarani, Shaini Patel, Avnesh S. Thakor, Jing Wang, Shobha Regmi, Lili Bettencourt
article en
5 citations

Abstract

In this study, we designed a nanoscale platform for sustained amino acid delivery to support transplanted pancreatic islets. The platform features mesoporous silica nanoparticles (MSNPs) loaded with glutamine (G), an essential amino acid required for islet survival and function, and coated with polydopamine (PD). We investigated various PD concentrations (0.5-2 mg/mL) and incubation times (0.5-2 h) to optimize G release, identifying that a PD concentration of 0.5 mg/mL incubated for 0.5 h yielded the best results to support islet viability and functionality <i>ex vivo</i>, particularly under inflammatory conditions. In syngeneic islet transplantation in STZ-diabetic mice, G alone provided only temporary benefits; however, PD-G-MSNPs significantly improved islet engraftment and function, with animals maintaining glycemic control for 30 days due to controlled G release. Our findings support the use of this nanoscale platform to provide essential nutrients like G to transplanted islets until they can establish their own blood and nutrient supply.

Nano LettersVol. 25(3)
Steno Diabetes Centers (DK), University of Miami (US), University of California, Los Angeles (US), Italian Institute of Technology (IT), Stanford University (US)
Stanford University, National Institute of Diabetes and Digestive and Kidney Diseases, Stanford Maternal and Child Health Research Institute
Zero hunger
Openalex Percentile: Top 2%
Pancreatic function and diabetes
10.03
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