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Antimicrobial activity, cytotoxicity and DNA binding studies of carbon dots

Authors :
Devanesan Arul Ananth
Mariadoss Asha Jhonsi
Arunkumar Kathiravan
Rekha Yamini
Soumen Bera
T. Sivasudha
Gayathri Nambirajan
Source :
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 196
Publication Year :
2017

Abstract

In recent years, quantum dots (QDs) are one of the most promising nanomaterials in life sciences community due to their unexploited potential in biomedical applications; particularly in bio-labeling and sensing. In the advanced nanomaterials, carbon dots (CDs) have shown promise in next generation bioimaging and drug delivery studies. Therefore the knowledge of the exact nature of interaction with biomolecules is of great interest to designing better biosensors. In this study, the interaction between CDs derived from tamarind and calf thymus DNA (ct-DNA) has been studied by vital spectroscopic techniques, which revealed that the CDs could interact with DNA via intercalation. The apparent association constant has been deduced from the absorption spectral changes of ct-DNA-CDs using the Benesi-Hildebrand equation. From the DNA induced emission quenching experiments the apparent DNA binding constant of the CDs (Kapp) have also been evaluated. Furthermore, we have analyzed the antibacterial and antifungal activity of CDs using disc diffusion assay method which exhibited excellent activity against E. coli and C. albicans with inhibition zone in the range of 7-12mm. The biocompatible nature of CDs was confirmed by an in vitro cytotoxicity test on L6 normal rat myoblast cells by using MTT assay. The cell viability is not affected till the high dosage of CDs (200μg/mL) for >48h. As a consequence of the work, future development of CDs for microbial control and DNA sensing among the various biomolecules is possible in view of emerging biofields.

Details

ISSN :
18733557
Volume :
196
Database :
OpenAIRE
Journal :
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
Accession number :
edsair.doi.dedup.....03258c12225fb6b6a6c1f45ed08037b2