Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0378-5173(03)00408-3
Title: Ultrasonication of chitosan and chitosan nanoparticles
Authors: Tang, E.S.K.
Huang, M. 
Lim, L.Y. 
Keywords: Chitosan nanoparticles
Mv
Particle size
Storage
TEM
Ultrasonic
Issue Date: 20-Oct-2003
Citation: Tang, E.S.K., Huang, M., Lim, L.Y. (2003-10-20). Ultrasonication of chitosan and chitosan nanoparticles. International Journal of Pharmaceutics 265 (1-2) : 103-114. ScholarBank@NUS Repository. https://doi.org/10.1016/S0378-5173(03)00408-3
Abstract: The objective of this study was to evaluate the effects of ultrasonication on chitosan molecules and nanoparticles. Molecular weight (Mv) of chitosan HCl (Mv 146kDa and degree of deacetylation (DD) 96%) decreased linearly with increasing duration and amplitude of ultrasonication. DD and FTIR absorption were unaffected. X-ray diffraction (XRD) analysis suggested greater chain alignment in the ultrasonicated chitosan samples. Chitosan nanoparticles had mean diameter of 382nm, polydispersity of 0.53 and zeta potential of 47mV. Ultrasonication administered at increasing duration or amplitude decreased the mean diameter and polydispersity of the nanoparticles. Zeta potential and FTIR absorbance were unaffected, while XRD suggested a greater disarray of chain alignment in the nanoparticle matrix. Under the transmission electron microscope (TEM), freshly prepared nanoparticles were dense spherical structures which became fragmented after ultrasonication for 10min at amplitude of 80. Untreated nanoparticle formulation turned turbid upon storage for 3 weeks at ambient conditions due to substantial swelling of the nanoparticles. Ultrasonicated nanoparticle formulation remained clear on storage. Although the particles had also swelled, they were no longer spherical, assuming instead an irregular shape with branching arms. In conclusion, high-intensity ultrasonication induced considerable damage on the chitosan nanoparticles which could affect their function as drug carriers. © 2003 Elsevier B.V. All rights reserved.
Source Title: International Journal of Pharmaceutics
URI: http://scholarbank.nus.edu.sg/handle/10635/106480
ISSN: 03785173
DOI: 10.1016/S0378-5173(03)00408-3
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