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Review Article | OPEN ACCESS

Characterization of Carbamazepine-Loaded Solid Lipid Nanoparticles Prepared by Rapid Expansion of Supercritical Solution

Zahra Akbari1 , Massoud Amanlou2, Javad Karimi-Sabet3, Abolfazl Golestani4, Mojtaba Shariaty Niasar5

1School of Chemical Engineering, Collage of Engineering, University of Tehran; 2Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences; 3Jaber Ebne Hayyan National Research Laboratory, NSTRI; 4Department of Biochemistry, Tehran University of Medical Sciences; 5School of Chemical Engineering, Collage of Engineering, University of Tehran, Tehran, Iran.

For correspondence:-  Zahra Akbari   Email: zakbary@ut.ac.ir   Tel:+989126161892

Received: 19 June 2014        Accepted: 24 October 2014        Published: 15 December 2014

Citation: Akbari Z, Amanlou M, Karimi-Sabet J, Golestani A, Niasar MS. Characterization of Carbamazepine-Loaded Solid Lipid Nanoparticles Prepared by Rapid Expansion of Supercritical Solution. Trop J Pharm Res 2014; 13(12):1955-1961 doi: 10.4314/tjpr.v13i12.1

© 2014 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To prepare carbamazepine-loaded solid lipid nanoparticles (CBZ-SLN) for prolonged release of CBZ in oral drug delivery.
Methods: CBZ-loaded SLNs were prepared by rapid expansion of supercritical solution (RESS). SLNs were formulated using stearic acid as the lipid component. Initially, lipid and drug were separately micronized by RESS process separately. This was followed by co-precipitation of the components with the two solutes using RESS to produce drug-loaded SLNs. The formulations were characterized by infrared spectroscopy (IR), scanning electron microscopy (SEM) and ultraviolet spectrophotometry (UV).
Results: Application of RESS to pure stearic acid yielded spherical particles in the range 40 to 200 nm which was about 600 times smaller than the unprocessed powder based on SEM observation. Similarly, RESS processing of carbamazepine produced nanoparticles with rod shape. FT-IR analysis showed that no chemical structure change occurred during RESS processing of both components. Co-precipitation of drug and lipid using RESS produced SLNs with drug loading capacity of 2.2 %. RESS yielded ultrafine spherical particles (100 nm) of CBZ-SLNs.
Conclusion: The successful preparation and characterization of carbamazepine-loaded solid lipid nanoparticles by RESS as well as their characterization has been achieved in this study.

Keywords: Rapid expansion of supercritical fluid, Stearic acid, Solid lipid nanoparticles, Carbamaze

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Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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