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Physicochemical, electrochemical, and biological characterization of field assisted gold nanocluster-coated barium titanate nanoparticles for biomedical applications

Authors
Sood, AnkurSinghmar, RituSahoo, SumantaLee, DahaeKim, Chul MinKumar, AnujHan, Sung Soo
Issue Date
Jan-2024
Publisher
Royal Society of Chemistry
Citation
Journal of Materials Chemistry B, v.12, no.2, pp 525 - 539
Pages
15
Indexed
SCIE
SCOPUS
Journal Title
Journal of Materials Chemistry B
Volume
12
Number
2
Start Page
525
End Page
539
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/69067
DOI
10.1039/d3tb01928d
ISSN
2050-7518
2050-750X
Abstract
Fluorescence-based bioimaging is an imperative approach with high clinical relevance in healthcare applications and biomedical research. The field of bioimaging plays an indispensable role in gaining insight into the internal architecture of cells/tissues and comprehending the physiological functions associated with biological systems. With the utility of piezoelectric nanomaterials, the bioelectric interface has been significantly investigated, leading to remarkable clinical relevance. Herein, we have developed barium titanate nanoparticle (BT) coated gold nanoclusters (AuNCs) in the presence and absence of an electromagnetic field (EMF). In this work, the effect of low (0.6 G) and high (2.0 G) EMFs on the structural arrangement of these piezoelectric nanocomposites (ABT) has been extensively studied with the help of X-ray diffraction (XRD), high diffraction resolution transmission electron microscopy (HR-TEM) and X-ray photoelectron spectroscopy (XPS). Furthermore, the two derivatives of ABT i.e. 0.6 ABT and 2.0 ABT have been evaluated for electrochemical behavior for their applicability as a candidate for exploring the bioelectric interface. Additionally, ABT, 0.6 ABT, and 2.0 ABT have been explored for cytocompatibility and bioimaging applications. The proposed piezoelectric nanocomposite, as a multifunctional platform, has enormous proficiency in the field of bioimaging and the capability to be utilized across the bioelectric interface. © 2024 The Royal Society of Chemistry.
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