4.4 Article

Outstanding Enhancement of Curcumin Fluorescence in PDDA and Silica Nanoparticles Coated DMPC Liposomes Based Nanocapsules: Application for Selective Estimation of ATP

Journal

CHEMISTRYSELECT
Volume 6, Issue 25, Pages 6324-6332

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202101386

Keywords

ATP; Curcumin; DMPC; Fluorescence; Liposome; Nanostructures; PDDA; Silica Nanoparticles

Funding

  1. American University of Beirut, Lebanon through University Research Board (URB)

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The study synthesized DMPC nanocapsules using nanotechnological modification of probe molecules to selectively target ATP molecules, demonstrating good stability.
Here we illustrate the synthesis of, 2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) liposome based poly(dimethyldiallylammonium chloride) (PDDA) nanocapsule where PDDA and silica nanoparticles are coated on the surface of curcumin embedded liposomes. The prepared nanocapsule was analyzed using UV-vis spectroscopy, fluorescence spectroscopy, Dynamic Light Scattering technique, Scanning Electron Microscopy, Zeta-potential, Thermogravimetric analysis and X-ray diffraction method. The fluorescence intensity of DMPC nanocapsules was found to be exceedingly, 60-fold, higher than free curcumin, thus, it boosts potential of such nanocapsules for various applications. The detection of Adinosine Triphosphate (ATP) was carried out by monitoring the change in the fluorescence emission of this DMPC nanocapsules while increasing the concentration of ATP molecule in the tested sample. Interestingly, fluorescence of free curcumin did not respond to ATP, whereas the fluorescence intensity of nanocapsules increased by the increase of ATP concentration, which establishes that materials prepared using nanotechnological modification of probe molecule can selectively target a particular analytical species. The nanocapsules based probe gave a linear correlation between the fluorescence intensity of DMPC nanocapsules in the concentration range 1 mu M -100 mu M with the limit of detection equals to 0.5 mu M. The described method is not interfered by uracil triphosphate, guanine triphosphate, cytosine triphosphate and thymine triphosphate molecules and showed good stability.

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