Crystallization, Luminescence and Cytocompatibility of Hexagonal Calcium Doped Terbium Phosphate Hydrate Nanoparticles

• Published in: Nanomaterials (Basel, Switzerland) Switzerland), 2021-01, Vol.11 (2), p.322
• Main Authors: Gómez-Morales, Jaime, Fernández-Penas, Raquel, Romero-Castillo, Ismael, Verdugo-Escamilla, Cristóbal, Choquesillo-Lazarte, Duane, D'Urso, Annarita, Prat, Maria, Fernández-Sánchez, Jorge Fernando
• Format: Article
• Language: English
• Subjects: Biocompatibility; Biomedical materials; Calcium; Calcium carbonate; calcium doped; Calcium ions; Calcium phosphates; Cell viability; citrate; Citric acid; Crystallization; cytocompatibility; Cytotoxicity; Doping; Electrophoretic mobility; Fluorescence; Fluorescence spectroscopy; Fourier transforms; Inductively coupled plasma; Ionic strength; Isometric; Lanthanide phosphates; Light scattering; Luminescence; Maturation; Medical imaging; Morphology; Nanocrystals; Nanomaterials; Nanoparticles; Nanophosphors; Optical properties; Photon correlation spectroscopy; Plasma spectra; Precision medicine; Quantum dots; Reagents; Software; Spectroscopy; Spectrum analysis; Terbium; terbium phosphates; Thermal analysis; Thermogravimetry; Tumor cell lines
• ISSN: 2079-4991; 2079-4991
• DOI: 10.3390/nano11020322

Luminescent lanthanide-containing biocompatible nanosystems represent promising candidates as nanoplatforms for bioimaging applications. Herein, citrate-functionalized calcium-doped terbium phosphate hydrate nanophosphors of the rhabdophane type were prepared at different synthesis times and different Ca /Tb ratios by a bioinspired crystallization method consisting of thermal decomplexing of Ca /Tb /citrate/phosphate/carbonate solutions. Nanoparticles were characterized by XRD, TEM, SEM, HR-TEM, FTIR, Raman, Thermogravimetry, inductively coupled plasma spectroscopy, thermoanalysis, dynamic light scattering, electrophoretic mobility, and fluorescence spectroscopy. They displayed ill-defined isometric morphologies with sizes ≤50 nm, hydration number n ~ 0.9, tailored Ca content (0.42-8.11 wt%), and long luminescent lifetimes (800-2600 µs). Their relative luminescence intensities in solid state are neither affected by Ca , citrate content, nor by maturation time for Ca doping concentration in solution below 0.07 M Ca . Only at this doping concentration does the maturation time strongly affect this property, decreasing it. In aqueous suspensions, neither pH nor ionic strength nor temperature affect their luminescence properties. All the nanoparticles displayed high cytocompatibility on two human carcinoma cell lines and cell viability correlated positively with the amount of doping Ca . Thus, these nanocrystals represent promising new luminescent nanoprobes for potential biomedical applications and, if coupled with targeting and therapeutic moieties, they could be effective tools for theranostics.