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Pharmaceutical characterization of solid and dispersed carbon nanotubes as nanoexcipients

Authors Ivanova, Lamprecht, Loureiro, Huzil JT, Foldvari M

Received 20 October 2011

Accepted for publication 20 November 2011

Published 26 January 2012 Volume 2012:7 Pages 403—415


Review by Single-blind

Peer reviewer comments 2

Marina V Ivanova1, Constanze Lamprecht1, M Jimena Loureiro1, J Torin Huzil1,2, Marianna Foldvari1

1School of Pharmacy, 2Faculty of Applied Mathematics, University of Waterloo, Waterloo, ON, Canada

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.

Keywords: carbon nanotubes, pharmaceutical characterization, Raman spectroscopy, thermogravimetric analysis, ultraviolet-visible near infrared spectroscopy

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