Tailoring the structure and self-activated photoluminescence of carbonated amorphous calcium phosphate nanoparticles for bioimaging applications

被引:1
|
作者
Machado, Thales R. [1 ]
Zanardo, Carlos E. [1 ]
Vilela, Raquel R. C. [1 ]
Miranda, Renata R. [1 ]
Moreno, Natalia S. [1 ]
Leite, Celisnolia M. [1 ]
Longo, Elson [2 ]
Zucolotto, Valtencir [1 ]
机构
[1] Univ Sao Paulo, Phys Inst Sao Carlos, GNANO Nanomed & Nanotoxicol Grp, BR-13566590 Sao Carlos, SP, Brazil
[2] Univ Fed Sao Carlos, CDMF Ctr Dev Funct Mat, BR-13565905 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
SENSITIVE DRUG-RELEASE; HYDROXYAPATITE NANOPARTICLES; IN-VITRO; LUMINESCENT HYDROXYAPATITE; APATITE NANOCRYSTALS; CITRATE STABILIZES; PH; CRYSTALLIZATION; ADSORPTION; MORPHOLOGY;
D O I
10.1039/d3tb02915h
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Self-activated luminescent calcium phosphate (CaP) nanoparticles, including hydroxyapatite (HA) and amorphous calcium phosphate (ACP), are promising for bioimaging and theragnostic applications in nanomedicine, eliminating the need for activator ions or fluorophores. In this study, we developed luminescent and stable citrate-functionalized carbonated ACP nanoparticles for bioimaging purposes. Our findings revealed that both the CO32- content and the posterior heating step at 400 degrees C significantly influenced the composition and the structural ordering of the chemically precipitated ACP nanoparticles, impacting the intensity, broadness, and position of the defect-related photoluminescence (PL) emission band. The heat-treated samples also exhibited excitation-dependent PL under excitation wavelengths typically used in bioimaging (lambda exc = 405, 488, 561, and 640 nm). Citrate functionalization improved the PL intensity of the nanoparticles by inhibiting non-radiative deactivation mechanisms in solution. Additionally, it resulted in an increased colloidal stability and reduced aggregation, high stability of the metastable amorphous phase and the PL emission for at least 96 h in water and supplemented culture medium. MTT assay of HepaRG cells, incubated for 24 and 48 h with the nanoparticles in concentrations ranging from 10 to 320 mu g mL-1, evidenced their high biocompatibility. Internalization studies using the nanoparticles self-activated luminescence showed that cellular uptake of the nanoparticles is both time (4-24 h) and concentration (160-320 mu g mL-1) dependent. Experiments using confocal laser scanning microscopy allowed the successful imaging of the nanoparticles inside cells via their intrinsic PL after 4 h of incubation. Our results highlight the potential use of citrate-functionalized carbonated ACP nanoparticles for use in internalization assays and bioimaging procedures. The optimization of carbonates concentration, a posterior heat treatment step, and citrate functionalization yield stable self-activated luminescent amorphous calcium phosphate nanoparticles for bioimaging applications.
引用
收藏
页码:4945 / 4961
页数:17
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