Literature DB >> 23606942

BLOOD TRIGGERED RAPID RELEASE POROUS NANOCAPSULES.

Tiffany P Gustafson1, Sergey A Dergunov, Walter J Akers, Qian Cao, Selena Magalotti, Samuel Achilefu, Eugene Pinkhassik, Mikhail Y Berezin.   

Abstract

Rapid-release drug delivery systems present a new paradigm in emergency care treatments. Such systems combine a long shelf life with the ability to provide a significant dose of the drug to the bloodstream in the shortest period of time. Until now, development of delivery formulations has concentrated on slow release systems to ensure a steady concentration of the drug. To address the need for quick release system, we created hollow polyacrylate nanocapsules with nanometer-thin porous walls. Burst release occurs upon interaction with blood components that leads to escape of the cargo. The likely mechanism of release involves a conformational change of the polymer shell caused by binding albumin. To demonstrate this concept, a near-infrared fluorescent dye indocyanine green (ICG) was incorporated inside the nanocapsules. ICG-loaded nanocapsules demonstrated remarkable shelf life in aqueous buffers with no release of ICG for twelve months. Rapid release of the dye was demonstrated first in vitro using albumin solution and serum. SEM and light scattering analysis demonstrated the retention of the nanocapsule architecture after the release of the dye upon contact with albumin. In vivo studies using fluorescence lifetime imaging confirmed quick discharge of ICG from the nanocapsules following intravenous injection.

Entities:  

Keywords:  ICG; drug release; emergency medicine; fluorescence lifetime; optical imaging

Year:  2013        PMID: 23606942      PMCID: PMC3627417          DOI: 10.1039/C3RA22693J

Source DB:  PubMed          Journal:  RSC Adv        ISSN: 2046-2069            Impact factor:   3.361


  43 in total

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Review 5.  Fluorescence anisotropy (polarization): from drug screening to precision medicine.

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  6 in total

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