Eco-friendly synthesis of surface grafted Carbon nanotubes from sugarcane cubes for development of prolonged release drug delivery platform

IF 1.2 Q4 NANOSCIENCE & NANOTECHNOLOGY
R. Narkhede, Mahesh P. More, Swapnil Patil, P. Patil, A. G. Patil, Prashant K. Deshmukh
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Abstract

Surface grafting of nanocarriers could modulate their properties and characteristics. As carbon nanotubes synthesis is a very tricky process and requires high-end methods, hence the present investigation was aimed to develop an eco-friendly method for synthesis carbon nanotubes (CNTs) and subsequent surface grafting for enhanced drug delivery application. The present study elaborates two-step chemical modifications; wherein the first step is catalytic cleavage of natural precursor in the presence of ferrocene and the second step involve chemical grafting of Acyclovir (ACV) as a model drug to understand the drug release behaviour. The catalytic cleavage of sugarcane cubes (natural precursor) was carried out in a closed copper tube, which prevents oxidation and results in a conversion of tubular nanostructures to amorphous carbon. The covalent attachment of ACV on purified CNTs (fCNTs) was done using carbodiimide chemistry. The preliminary Uv-Vis absorbance spectra defined at 260 nm was arised due to π-π* stacking of aromatic C-C bonds. The Fourier Transforms Infrared Spectroscopy (FTIR) indicated the hydroxyl stretch at 3300 cm-1 while amide I bond formation was observed at 1672 cm-1. The XRD spectra confirmed successful synthesis of CNTs. The calculated average crystallite size (Scherer equation) of synthesized CNTs was found to be 42.84 and 44.45 nm; it was also in accordance with the morphological observation as confirmed simultaneously using SEM analysis. The covalently attached ACV was released up to 80% during 8h of in vitro drug release study. The surface grafting potential of CNTs was found to be promising compared to other nanomaterials.
甘蔗块表面接枝碳纳米管的环保合成及其缓释给药平台的开发
纳米载体的表面接枝可以改变其性质和特性。由于碳纳米管的合成是一个非常棘手的过程,并且需要高端的方法,因此本研究旨在开发一种环保的碳纳米管(CNTs)合成和随后的表面接枝方法,以增强药物传递应用。本研究阐述了两步化学修饰;其中第一步是在二茂铁存在下催化裂解天然前体,第二步是将阿昔洛韦(ACV)作为模型药物进行化学接枝,以了解药物释放行为。甘蔗立方体(天然前驱体)的催化裂解在封闭的铜管中进行,防止氧化并导致管状纳米结构转化为无定形碳。ACV在纯化碳纳米管(fCNTs)上的共价附着采用碳二亚胺化学方法。由于芳香族C-C键的π-π*堆叠,在260 nm处产生了初步的紫外-可见吸收光谱。傅里叶变换红外光谱(FTIR)表明羟基在3300 cm-1处拉伸,酰胺I键在1672 cm-1处形成。XRD谱图证实了CNTs的成功合成。合成CNTs的平均晶粒尺寸(Scherer方程)分别为42.84 nm和44.45 nm;同时用扫描电镜(SEM)分析证实,这与形态学观察一致。体外释药试验8h,共价附着的ACV释药率高达80%。与其他纳米材料相比,CNTs的表面接枝潜力更大。
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来源期刊
international journal of nano dimension
international journal of nano dimension NANOSCIENCE & NANOTECHNOLOGY-
CiteScore
2.80
自引率
20.00%
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0
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