Biocompatible Carbon Nanodots for Functional Imaging and Cancer Therapy: Carbon Nanodots for Imaging and Cancer Therapy

Biocompatible Carbon Nanodots for Functional Imaging and Cancer Therapy: Carbon Nanodots for Imaging and Cancer Therapy

Alexandre Roumenov Loukanov (Saitama University, Saitama, Japan), Hristo Stefanov Gagov (Sofia University, Sofia, Bulgaria), Milena Yankova Mishonova (Sofia University, Sofia, Bulgaria) and Seiichiro Nakabayashi (Saitama University, Saitama, Japan)
Copyright: © 2018 |Pages: 15
DOI: 10.4018/IJBCE.2018070103

Abstract

This article describes how carbon quantum dots (C-dots) are tiny carbon nanoparticles (less than 10 nm in size) being envisaged to be used in bio-sensing, bio-imaging and drug delivery nanosystems. Their low toxicity and stable chemical properties make them suitable candidates for new types of fluorescent probe, which overcome the common drawbacks of previous fluorescent probes (organic dyes and inorganic quantum dots). In addition, fluorescent C-dots possess a rather strong ability to bind with other organic and inorganic molecules due to their abundant surface groups. For that reason, fluorescent C-dots can be manipulated via series of controllable chemical treatments in order to satisfy the demands in the photocatalytic, biochemical and chemical sensing, bio-imaging, drug delivery and enhanced cell targeting. In recent studies it was described the development of carbon quantum dots with large two-photon absorption cross sections towards two-photon imaging for use in photodynamic cancer therapy. Thus, C-dots have become a rising star in biomedical research with a promising future for the application in nanomedicine.
Article Preview

2. Fabrication Of Biocompatible Carbon Nanodots As Functional Imaging Agents

The fabrication methods for carbon nanodots with tunable size can generally be classified into two main approaches: bottom-up and top-down (Li, 2012; Zuo, 2015). Top-down preparations of fluorescence C-dots are the early preparation approaches, including arc-discharge method (Li, 2012; Jian, 2010;), electrochemical oxidation (Zheng, 2009; Lu, 2009; Zhou, 2007; Zhao, 2008), and laser ablation (Yang, 2009; Goncalves, 2010). Compared with the multistep preparation method of C-dots, one-step reaction processes not only simplify the preparation procedure, but also these C-dots are with better fluorescent properties. Additionally, thus created C-dots may express special fluorescent properties by using various organic reaction solution. Bottom-up approaches are based on the polymerization reaction for small molecules to the formation of nanoscale C-dots. This strategy includes hydrothermal method (Liu, 2007; Wang, 2013; Qian, 2014; Xu, 2014; Dong, 2014; Gao, 2013; Ray, 2009), microwave-assisted pyrolysis method (Tang, 2014; Zhu, 2009; Wang, 2012; Chandra, 2011; Yang, 2012), ultrasonic method (Oza, 2015), acid dehydration method (Lecroy, 2014), and pyrolysis method (Bourlinos, 2008; Zong, 2014). Among them, the most widely used are the hydrothermal method and microwave-assisted pyrolysis method, which can be realized by the one-step method for preparing fluorescent C-dots with high quantum yield (QY > 50%). Thus, nanoparticles with diameter between 1–2 nm are formed spontaneously in one-step thermal treatment from different organic materials and are sufficiently well characterized by different structural methods. The C-dot hydrophobic core is made of pure carbon (consisted of aromatic domains) that is surrounded by polar (hydroxyl, carboxyl, amino, carbonyl and epoxy) and alkyl surface groups as shown on Figure 1. The organic functional groups make the nanoparticles highly soluble in aqueous media and help their penetration through the cell membrane mainly by endocytosis.

Complete Article List

Search this Journal:
Reset
Open Access Articles: Forthcoming
Volume 9: 2 Issues (2020): Forthcoming, Available for Pre-Order
Volume 8: 2 Issues (2019): 1 Released, 1 Forthcoming
Volume 7: 2 Issues (2018)
Volume 6: 2 Issues (2017)
Volume 5: 2 Issues (2016)
Volume 4: 2 Issues (2015)
Volume 3: 2 Issues (2014)
Volume 2: 2 Issues (2013)
Volume 1: 2 Issues (2012)
View Complete Journal Contents Listing