生物相容性材料
壳聚糖
纳米探针
纳米技术
材料科学
电化学
化学
化学工程
纳米颗粒
电极
生物医学工程
生物化学
物理化学
医学
工程类
作者
Jagriti Gupta,Kishan Das,Ayushi Tanwar,Paulraj Rajamani,Jaydeep Bhattacharya
标识
DOI:10.1016/j.molliq.2022.119193
摘要
• Electrochemical approach was used to study the interaction between MPA-CdSe QDs and chitosan for development of biocompatible theranostic nanoprobe. • The electrochemical study revealed an interaction of chitosan with CdSe QDs at the ratio of 1.3:1 and a binding constant of approx 10 15 L Mol −1 . • Cell viability assay confirms the less cytotoxicity of chitosan coated QDs in healthy cell lines and more anticancerous activity in cancerous cell lines. • Confocal Microscopy and Z stacking confirms the efficacy of chitosan coated QDs as bioimaging nanoprobe. The strength and stability of biopolymer-modified quantum dots (QDs) for designing biocompatible nanoprobes depends on the interaction between QDs and coating of interest. Hence, the quantitative determination of interaction parameters has a crucial role in their development. This paper focuses on an electrochemical approach to determine interaction and binding parameters between the chitosan and hydrophilic Mercaptopropionic acid (MPA) - CdSe QDs. MPA- CdSe QDs were synthesized by the hot injection method and characterized by several techniques. The cyclic voltammetry study revealed the reduction in oxidation peak current of redox solution with the addition of MPA- CdSe QDs (50 × 10 −12 M to 350 × 10 −12 M); however, the peak current was increased with the addition of chitosan (1 × 10 −13 M to 50 × 10 −13 M), without any change in the oxidation potential. This may be due to the interaction of the amino group of chitosan with the carboxylate group of MPA-CdSe QDs. The interaction was analyzed in terms of binding constant and no. of binding sites, which was 7.3 × 10 15 L Mol −1 and 1.3, respectively. Effect of scan rate on oxidation and reduction peak current confirms an irreversible electrode reaction. The interaction was further characterized with UV–Vis/Fluorescence spectroscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. Biocompatibility of developed nano-biocomposite further evaluated by standard cell viability assay using Adenocarcinoma human alveolar basal epithelial cell line (A549) and Chinese hamster cell line (V79). Confocal microscopic studies and Z stacking were also performed to explore the efficacy of chitosan-coated MPA-CdSe QDs as a fluorescent agent for cell imaging.
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