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Spiropyran-Conjugated Pluronic as a Dual Responsive Colorimetric Detector
Novel spiropyran‐conjugated Pluronic [polyethylene oxide (PEO)‐b‐polypropylene oxide (PPO)‐b‐polyethylene oxide (PEO)] micelles are developed as a new colorimetric detector showing photo‐ or thermo‐switchable behavior. Facile conjugation of spiropyran to Pluronic was confirmed by 1H NMR, UV–Vis, and...
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Published in: | Macromolecular rapid communications. 2012-11, Vol.33 (22), p.1958-1963 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Novel spiropyran‐conjugated Pluronic [polyethylene oxide (PEO)‐b‐polypropylene oxide (PPO)‐b‐polyethylene oxide (PEO)] micelles are developed as a new colorimetric detector showing photo‐ or thermo‐switchable behavior. Facile conjugation of spiropyran to Pluronic was confirmed by 1H NMR, UV–Vis, and Fluorescence spectroscopy. A switchable photoluminescence is found depending on the irradiation with either UV or visible light, and temperature resulting from structural isomerization of spiropyran between spiropyran (SP) and merocyanine (MC) form. Cytotoxicity of the spiropyran‐conjugated Pluronic (SP‐PL) was evaluated following an MTT assay, whereas photo responsiveness of spiropyran within the micelles was determined by confocal laser scanning microscopy.
A biocompatible photo and thermoresponsivespiropyran‐conjugated Pluronic has been synthesized. The spiropyran retains its photochromic properties within the polymer after exposure to different condition. SP form of SP‐PL is colorless but after irradiation with UV–Vis light, it converts to purple‐colored zwitterionic MC form wherein after exposure to heat orange‐colored quoinoidal form is appeared. |
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ISSN: | 1022-1336 1521-3927 |
DOI: | 10.1002/marc.201200416 |