Aqueous synthesis of tunable fluorescent, semiconductor CuInS2 quantum dots for bioimaging
Herein, we have presented a unique strategy for aqueous synthesis of semiconductor CuInS2 QDs which showed multiple fluorescence. These synthesized CuInS2 QDs were prepared in aqueous media with biocompatible glutathione (GSH), as capping ligand and stabilizer, while the fluorescence and crystallini...
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doaj-2833930df8564104abbe630709ab3c332020-11-25T01:11:16ZengElsevierArabian Journal of Chemistry1878-53522019-12-0112848404847Aqueous synthesis of tunable fluorescent, semiconductor CuInS2 quantum dots for bioimagingAnila Arshad0Raheel Akram1Saleem Iqbal2Fozia Batool3Bushra Iqbal4Bilal Khalid5Arif Ullah Khan6Beijing University of Chemical Technology, ChinaBeijing University of Chemical Technology, China; Corresponding author.Beijing University of Chemical Technology, ChinaUniversity of Sargodha, PakistanBeijing University of Chemical Technology, ChinaTsinghua University, ChinaBeijing University of Chemical Technology, ChinaHerein, we have presented a unique strategy for aqueous synthesis of semiconductor CuInS2 QDs which showed multiple fluorescence. These synthesized CuInS2 QDs were prepared in aqueous media with biocompatible glutathione (GSH), as capping ligand and stabilizer, while the fluorescence and crystallinity were controlled by varying the reaction time. The investigation of various other experimental parameters including precursor’s concentration, effect of pH, and stability of QDs has also been carried out. These QDs were characterized by XRD, TEM, and FT-IR. Meanwhile, optical properties of as synthesized QDs were also investigated by fluorescence spectroscopy. Furthermore, the synthesized QDs were also less cytotoxic and maintained remarkable cell viability up to 100 μg/mL. When bioconjugated with Arginyl-glycyl-aspartic acid (RGD) moiety, the obtained CuInS2-RGD QDs have shown higher biocompatibility and good bioimaging performance. Keywords: Aqueous synthesis, CuInS2, Quantum dots, Fluorescence, Bioimaginghttp://www.sciencedirect.com/science/article/pii/S1878535216301708 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Anila Arshad Raheel Akram Saleem Iqbal Fozia Batool Bushra Iqbal Bilal Khalid Arif Ullah Khan |
spellingShingle |
Anila Arshad Raheel Akram Saleem Iqbal Fozia Batool Bushra Iqbal Bilal Khalid Arif Ullah Khan Aqueous synthesis of tunable fluorescent, semiconductor CuInS2 quantum dots for bioimaging Arabian Journal of Chemistry |
author_facet |
Anila Arshad Raheel Akram Saleem Iqbal Fozia Batool Bushra Iqbal Bilal Khalid Arif Ullah Khan |
author_sort |
Anila Arshad |
title |
Aqueous synthesis of tunable fluorescent, semiconductor CuInS2 quantum dots for bioimaging |
title_short |
Aqueous synthesis of tunable fluorescent, semiconductor CuInS2 quantum dots for bioimaging |
title_full |
Aqueous synthesis of tunable fluorescent, semiconductor CuInS2 quantum dots for bioimaging |
title_fullStr |
Aqueous synthesis of tunable fluorescent, semiconductor CuInS2 quantum dots for bioimaging |
title_full_unstemmed |
Aqueous synthesis of tunable fluorescent, semiconductor CuInS2 quantum dots for bioimaging |
title_sort |
aqueous synthesis of tunable fluorescent, semiconductor cuins2 quantum dots for bioimaging |
publisher |
Elsevier |
series |
Arabian Journal of Chemistry |
issn |
1878-5352 |
publishDate |
2019-12-01 |
description |
Herein, we have presented a unique strategy for aqueous synthesis of semiconductor CuInS2 QDs which showed multiple fluorescence. These synthesized CuInS2 QDs were prepared in aqueous media with biocompatible glutathione (GSH), as capping ligand and stabilizer, while the fluorescence and crystallinity were controlled by varying the reaction time. The investigation of various other experimental parameters including precursor’s concentration, effect of pH, and stability of QDs has also been carried out. These QDs were characterized by XRD, TEM, and FT-IR. Meanwhile, optical properties of as synthesized QDs were also investigated by fluorescence spectroscopy. Furthermore, the synthesized QDs were also less cytotoxic and maintained remarkable cell viability up to 100 μg/mL. When bioconjugated with Arginyl-glycyl-aspartic acid (RGD) moiety, the obtained CuInS2-RGD QDs have shown higher biocompatibility and good bioimaging performance. Keywords: Aqueous synthesis, CuInS2, Quantum dots, Fluorescence, Bioimaging |
url |
http://www.sciencedirect.com/science/article/pii/S1878535216301708 |
work_keys_str_mv |
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