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Monitoring nanoparticle dissolution via fluorescence-colour shift

Ritschel, Christian 1; Napp, Joanna; Alves, Frauke ; Feldmann, Claus 1
1 Institut für Anorganische Chemie (AOC), Karlsruher Institut für Technologie (KIT)

Abstract:

[La(OH)]$^{2+}$[ICG]$^{−}$$_{2}$ and [La(OH)]$^{2+}$$_{2}$[PTC]$^{4−}$ inorganic–organic hybrid nanoparticles (IOH-NPs) with indocyanine green (ICG) and perylene-3,4,9,10-tetracarboxylate (PTC) as fluorescent dye anions are used for emission-based monitoring of the dissolution of nanoparticles. Whereas ICG shows a deep red emission in the solid [La(OH)]$^{2+}$[ICG]$^{−}$$_{2}$ IOH-NPs, the emission of PTC in the solid [La(OH)]$^{2+}$$_{2}$[PTC]$^{4−}$ IOH-NPs is completely quenched due to π-stacking. After nanoparticle dissolution, the emission of freely dissolved ICG is weak, whereas freely dissolved PTC shows intense green emission. We report on the synthesis of IOH-NPs and nanoparticle characterization as well as on the fluorescence properties and how to avoid undesirable energy transfer between different fluorescent dyes. The emission shift from red (intact solid nanoparticles) to green (freely dissolved dye anions), indicating nanoparticle dissolution, is shown for aqueous systems and verified $\textit{in vitro}$. Based on this first proof-of-the-concept, the IOH-NP marker system can be interesting to monitor nanoparticle dissolution in cells and tissues of small animals and to evaluate cell processes and/or drug-delivery strategies.


Verlagsausgabe §
DOI: 10.5445/IR/1000152874
Veröffentlicht am 18.11.2022
Originalveröffentlichung
DOI: 10.1039/d2nr03078k
Scopus
Zitationen: 2
Dimensions
Zitationen: 2
Cover der Publikation
Zugehörige Institution(en) am KIT Institut für Anorganische Chemie (AOC)
Publikationstyp Zeitschriftenaufsatz
Publikationsdatum 10.11.2022
Sprache Englisch
Identifikator ISSN: 2040-3364, 2040-3372
KITopen-ID: 1000152874
Erschienen in Nanoscale
Verlag Royal Society of Chemistry (RSC)
Band 14
Heft 43
Seiten 16249–16255
Nachgewiesen in Web of Science
Dimensions
Scopus
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