Schematic representation of functionalized CNTs with various molecules is given

in Figure 4. The functionalization can be divided into two main subcategories: noncovalent functionalization and covalent functionalization. Figure 4 Schematic illustration of functionalization of CNTs with various molecules: (a) Prakash et al. [18], (b) Xiao et al. [78], (c) Xu et al. [70], (d) Gomez-Gualdron et al. [64], (e) Bianco et Inhibitors,research,lifescience,medical al. [79], (f) Jiang et al. [80], (g) Williams et al. [81], and … 3.1. Covalent Functionalization Covalent functionalization of CNTs with the therapeutically kinase inhibitor Axitinib active molecule or the biocompatible surfactants is governed by the oxidation of CNTs using strong acids (conc. H2SO4 or conc. HNO3) which generates substitutable hydrophilic functional groups such as COOH and OH on the CNTs which then further undergo into the chemical Inhibitors,research,lifescience,medical reactions

such Inhibitors,research,lifescience,medical as esterification, amidation, chlorination, bromination, hydrogenation, and Diel’s-Alder reaction. In order to get functionalized with these active molecules, CNTs allow side-wall covalent attachment of functional groups by the inhibitor licensed addition of radicals, nucleophilic carbenes, nitrenes, nucleophilic cyclopropanation, and electrophiles [79, 83, 84]. The method of oxidation results in the opening of the CNT end caps, generating carboxylic groups suitable for enhancing the solubility of the CNTs with improved biocompatibility [85]. It has been shown that

a highly negative charge developed Inhibitors,research,lifescience,medical as a result of the carboxylation increases the hydrophilicity of CNTs. Covalent linkage of polyethylene glycols increases the hydrophilicity and the solubility of CNTs in aqueous media Inhibitors,research,lifescience,medical as well as increasing the size which reduces the rate of clearance of CNTs through the kidneys and tends to increase the circulation Anacetrapib time in the plasma. Tour et al. proposed the functionalization of CNTs in acidic media, which yields oxidized CNTs in large and industrial scale quantities [86]. Side wall functionalization of SWCNTs through C–N bond forming substitutions of fluoronanotubes was explored by Khabashesku et al. and reported that this method offers a wide range of further SWCNTs derivatizations including their covalent binding to amino acids, DNA, and polymer matrix [87]. 3.2. Noncovalent Functionalization Noncovalent functionalization involves Van der Waals interactions, π-π interactions, and hydrophobic interactions of biocompatible functional groups with the surface of the CNT.