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固体和分散碳纳米管作为纳米赋形剂的药物特性。

Pharmaceutical characterization of solid and dispersed carbon nanotubes as nanoexcipients.

机构信息

School of Pharmacy, University of Waterloo, Waterloo, ON, Canada.

出版信息

Int J Nanomedicine. 2012;7:403-15. doi: 10.2147/IJN.S27442. Epub 2012 Jan 25.

DOI:10.2147/IJN.S27442
PMID:22334774
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3273976/
Abstract

BACKGROUND

Carbon nanotubes (CNTs) are novel materials with considerable potential in many areas related to nanomedicine. However, a major limitation in the development of CNT-based therapeutic nanomaterials is a lack of reliable and reproducible data describing their chemical and structural composition. Knowledge of properties including purity, structural quality, dispersion state, and concentration are essential before CNTs see widespread use in in vitro and in vivo experiments. In this work, we describe the characterization of several commercially available and two in-house-produced CNT samples and discuss the physicochemical profiles that will support their use in nanomedicine.

METHODS

Eighteen single-walled and multi-walled CNT raw materials were characterized using established analytical techniques. Solid CNT powders were analyzed for purity and structural quality using thermogravimetric analysis and Raman spectroscopy. Extinction coefficients for each CNT sample were determined by ultraviolet-visible near infrared absorption spectroscopy. Standard curves for each CNT sample were generated in the 0-5 μg/mL concentration range for dispersions prepared in 1,2-dichlorobenzene.

RESULTS

Raman spectroscopy and thermogravimetric analysis results demonstrated that CNT purity and overall quality differed substantially between samples and manufacturer sources, and were not always in agreement with purity levels claimed by suppliers. Absorbance values for individual dispersions were found to have significant variation between individual single-walled CNTs and multi-walled CNTs and sources supplying the same type of CNT. Significant differences (P < 0.01) in extinction coefficients were observed between and within single-walled CNTs (24.9-53.1 mL·cm(-1)·mg(-1)) and multi-walled CNTs (49.0-68.3 mL·cm(-1)·mg(-1)). The results described here suggest a considerable role for impurities and structural inhomogeneities within individual CNT preparations and the resulting spectroscopic properties of their dispersions.

CONCLUSION

Raw CNT materials require thorough analytical workup before they can be used as nanoexcipients. This applies especially to the determination of CNT purity, structure, and concentration. The results presented here clearly demonstrate that extinction coefficients must be determined for individual CNT preparations prior to their use.

摘要

背景

碳纳米管(CNTs)是一种具有很大潜力的新型材料,在许多与纳米医学相关的领域都有应用。然而,基于 CNT 的治疗性纳米材料的发展主要受到缺乏可靠和可重复的数据来描述其化学和结构组成的限制。在 CNT 广泛应用于体外和体内实验之前,必须了解其纯度、结构质量、分散状态和浓度等特性。在这项工作中,我们描述了对几种市售和两种自制 CNT 样品的表征,并讨论了支持它们在纳米医学中应用的物理化学特性。

方法

使用已建立的分析技术对 18 种单壁和多壁 CNT 原材料进行了表征。使用热重分析和拉曼光谱对固态 CNT 粉末的纯度和结构质量进行了分析。通过紫外-可见近红外吸收光谱确定了每种 CNT 样品的消光系数。在 1,2-二氯苯中制备浓度为 0-5μg/mL 的分散体,为每个 CNT 样品生成标准曲线。

结果

拉曼光谱和热重分析结果表明,CNT 的纯度和整体质量在样品和制造商来源之间有很大差异,并且并不总是与供应商声称的纯度水平一致。发现单个单壁 CNT 和多壁 CNT 以及供应相同类型 CNT 的来源之间的单个分散体的吸光度值存在显著差异。在单壁 CNT(24.9-53.1mL·cm(-1)·mg(-1))和多壁 CNT(49.0-68.3mL·cm(-1)·mg(-1))之间以及单壁 CNT 内部观察到消光系数存在显著差异(P<0.01)。结果表明,单个 CNT 制剂中的杂质和结构不均匀性及其分散体的光谱特性起着重要作用。

结论

在将 CNT 材料用作纳米赋形剂之前,需要对原始 CNT 材料进行全面的分析工作。这尤其适用于 CNT 纯度、结构和浓度的确定。本文提出的结果清楚地表明,在使用 CNT 之前,必须确定每个 CNT 制剂的消光系数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/04bb3d848aae/ijn-7-403f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/7bcffb03976d/ijn-7-403f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/c5b55e74c9e3/ijn-7-403f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/ee1cc36a612e/ijn-7-403f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/7034d62661ed/ijn-7-403f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/8b47ee629982/ijn-7-403f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/04bb3d848aae/ijn-7-403f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/7bcffb03976d/ijn-7-403f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/c5b55e74c9e3/ijn-7-403f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/ee1cc36a612e/ijn-7-403f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/7034d62661ed/ijn-7-403f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/8b47ee629982/ijn-7-403f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287a/3273976/04bb3d848aae/ijn-7-403f6.jpg

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