articleJournal of the American Chemical SocietyMay 29, 2009Closed access

Mesoporous Silica Nanoparticle-Based Double Drug Delivery System for Glucose-Responsive Controlled Release of Insulin and Cyclic AMP

Iowa State University · Ames National Laboratory

PubMed
Indexed incrossrefpubmed

Abstract

A boronic acid-functionalized mesoporous silica nanoparticle-based drug delivery system (BA-MSN) for glucose-responsive controlled release of both insulin and cyclic adenosine monophosphate (cAMP) was synthesized. Fluorescein isothiocyanate-labeled, gluconic acid-modified insulin (FITC-G-Ins) proteins were immobilized on the exterior surface of BA-MSN and also served as caps to encapsulate cAMP molecules inside the mesopores of BA-MSN. The release of both G-Ins and cAMP was triggered by the introduction of saccharides. The selectivity of FITC-G-Ins release toward a series of carbohydrate triggers was determined to be fructose > glucose > other saccharides. The unique feature of this double-release system is…

Citation impact

765
total citations
FWCI
54.31
Percentile
100%
References
22
Citations per year

Authors

4

Topics & keywords

Keywords
  • Chemistry
  • Mesoporous silica
  • Mesoporous material
  • Fluorescein isothiocyanate
  • Biophysics
  • Fluorescein
  • Cyclic adenosine monophosphate
  • Drug delivery
No related works found for this paper.