๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Chemiluminescent PEG-PCL micelles for imaging hydrogen peroxide

โœ Scribed by Madhuri Dasari; Dongwon Lee; Venkata Reddy Erigala; Niren Murthy


Book ID
102295852
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
241 KB
Volume
89A
Category
Article
ISSN
1549-3296

No coin nor oath required. For personal study only.

โœฆ Synopsis


Abstract

Hydrogen peroxide is one of the fundamental molecules of biology, regulating key cell signaling pathways and the development of numerous inflammatory diseases. There is therefore great interest in developing contrast agents that can detect hydrogen peroxide in vitro and in vivo. In this report, we present a new contrast agent for imaging hydrogen peroxide, termed the chemiluminescent poly(ethylene glycol)โ€bโ€poly(ฯตโ€caprolactone) (PEGโ€PCL) micelles (CPMs), which can detect hydrogen peroxide at nanomolar concentrations and chemiluminesce in the near IR range (676 nm) in the presence of hydrogen peroxide. The CPMs are composed of a PEGโ€PCL scaffold and have fluorescent dyes and peroxalate esters in their hydrophobic PCL core. The CPMs image hydrogen peroxide by undergoing a threeโ€component chemiluminescent reaction involving a peroxalate ester, a fluorescent dye, and hydrogen peroxide. The CPMs also have a stealth PEG corona to enhance their circulation half life. The CPMs should find numerous applications for imaging hydrogen peroxide because of their nanomolar sensitivity, small size, and stealth pegylated surface. ยฉ 2009 Wiley Periodicals, Inc. J Biomed Mater Res, 2009


๐Ÿ“œ SIMILAR VOLUMES


Delivery of the photosensitizer Pc 4 in
โœ Alyssa M. Master; Myriam E. Rodriguez; Malcolm E. Kenney; Nancy L. Oleinick; Ani ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 439 KB

The silicon phthalocyanine Pc 4 is a second-generation photosensitizer that has several properties superior to other photosensitizers currently approved by the FDA, and it has shown significant promise for photodynamic therapy (PDT) in several cancer cells in vitro and model tumor systems in vivo. H