Pharmaceutical characterization of solid and dispersed carbon nanotubes as nanoexcipients

被引:50
作者
Ivanova, Marina V. [1 ]
Lamprecht, Constanze [1 ]
Loureiro, M. Jimena [1 ]
Huzil, J. Torin [1 ,2 ]
Foldvari, Marianna [1 ]
机构
[1] Univ Waterloo, Sch Pharm, Waterloo, ON N2L 3G1, Canada
[2] Univ Waterloo, Fac Appl Math, Waterloo, ON N2L 3G1, Canada
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2012年 / 7卷
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院; 加拿大创新基金会;
关键词
carbon nanotubes; pharmaceutical characterization; Raman spectroscopy; thermogravimetric analysis; ultraviolet-visible near infrared spectroscopy; RAMAN-SPECTROSCOPY; FUNCTIONAL EXCIPIENTS; IN-VITRO; NANOMEDICINES; DELIVERY; PURITY; DNA;
D O I
10.2147/IJN.S27442
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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 mu g/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.
引用
收藏
页码:403 / 415
页数:13
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