Ratiometric pH-nanosensors based on rhodamine-doped silica nanoparticles functionalized with a naphthalimide derivative
A naphthalimide derivative has been successfully immobilized on the outer surface of rhodamine-doped silica nanoparticles yielding pH-nanosensors able to monitor proton concentration in the biologically relevant pH-range. This paper describes the preparation of two-dye-doped silica nanoparticles for...
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Veröffentlicht in: | Journal of colloid and interface science 2009-11, Vol.339 (1), p.266-270 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A naphthalimide derivative has been successfully immobilized on the outer surface of rhodamine-doped silica nanoparticles yielding pH-nanosensors able to monitor proton concentration in the biologically relevant pH-range.
This paper describes the preparation of two-dye-doped silica nanoparticles for ratiometric pH measurements in the biologically relevant pH-range. While a rhodamine derivative is embedded in a silica core and used as the reference, a pH-sensitive naphthalimide dye is immobilized on the previously amino-functionalized core through two different approaches. Either the naphthalimide’s carboxylic group is activated to a succinimidyl-ester to form an amide bond or the system can be built up
via solid-phase organic synthesis in only two steps. Both types of nanosensors are characterized in terms of morphology (dynamic light scattering, transmission electron microscopy) and optical properties (steady-state fluorescence spectroscopy). In terms of application,
e.g. reproducibility and handling of the synthesis, the first approach gave very good results with respect to size and size distribution and a p
K
a value of 6.55 was found that is comparable to the free indicator dye in solution. The solid-phase organic synthesis method proves the possibility of covalent immobilization of naphthalimides to amino-functionalized surfaces, showing the stability of the polymeric substrate and achieving comparable results for pH sensing. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2009.07.044 |