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How to cite this article: Al-Azzawı S, Hammadı A, Masheta D. Anti-inflammatory activity of prednisolone drug loaded on carbon nanotubes. J Res
Pharm. 2024; 28(3): 651-660.
© 2024 Marmara University Press
ISSN: 2630-6344
http://dx.doi.org/10.29228/jrp.727
651
Anti-inflammatory activity of prednisolone drug loaded
on carbon nanotubes
Shafq AL-AZZAWI
1
* , Asmaa HAMMADI
1
, Dhafir MASHETA
1
1
College of Pharmacy, University of Babylon, Hilla, 51002, Iraq
* Corresponding Author. E-mail: phar.shafaq.kadhim@uobabylon.edu.iq (S.A.); Tel. +09647831349452.
Received: 18 April 2023 / Revised: 27 September 2023 / Accepted: 28 September 2023
ABSTRACT: The activity of many anti-inflammatory drugs is limited due to inadequate tissue penetration and targeting
efficiency and side effects of free drug. A properly designed delivery system can enhance therapeutic activity by
overcoming these obstacles. This study aims to load prednisolone drug molecules on carbon nanotubes carrier (CNT) for
improving its anti-inflammatory action and reducing the adverse reactions associated with using higher doses of the
unloaded drug. CNT carrier was loaded with prednisolone by nano-extraction, and the morphology and size were
determined by a scanning electron microscope. X-ray diffraction patterns and FT-IR spectra were utilized for
characterization. While the anti-inflammatory activity of the loaded drug was examined biochemically through the
assessment of interleukin-1 levels as an inflammatory marker using an in vitro tissue culture model composed of HeLa
cells. These cells were stimulated with TNF-α to initiate the activation of the nuclear factor-κB as an inflammatory
response. Successful loading of drug was confirmed through microscopic examination results which showed that CNT
formed a network with bundles of prednisolone molecules grafted onto the surface, and these results were confirmed by
X-ray diffraction and FT-IR. Whereas, the loaded drug still has its anti-inflammatory action, by significant lowering in
interleukin-1 levels which was detected in TNF-α-stimulated cells treated with prednisolone loaded on CNT compared
to unloaded CNT. In conclusion, this study demonstrated, for the first time, a successful loading of prednisolone to a
CNT with a potential anti-inflammatory action making it a promising complex in treating inflammatory diseases with
reduced therapeutic doses.
KEYWORDS: Anti-inflammatory action; Interleukin-1; Carbon nanotube; Prednisolone; Drug delivery systems
1. INTRODUCTION
The enhanced and improved understanding of disease biology and aetiology is revealing new
receptor targets for treatment. Nevertheless, due to insufficient tissue penetration and targeting efficiency,
such treatments aiming at these receptors frequently fail [1]. A deeper comprehension is necessary to
overcome obstacles with inadequate permeability across biological barriers and achieve targeted drug
delivery to various tissues at the cellular level [1].
Drug delivery systems (DDS), either simple or sophisticated, are designed to enhance the therapeutic
profile of biomolecules and protect them from deactivation while circulating in the body. Without DDS,
effectiveness is completely reliant on drug's physico-chemical characteristics and capacity to enter a target
region where the action is required. Safer (by decreasing the dose of administered drug) and more efficient
drug delivery (by improving specific tissues targeting) may be achieved by hiring of targeted nanomedicines
as DDS [2,3]. Thus, in the last two decades, the applications of nanomaterials (such as liposomes,
dendrimers, carbon and titanium dioxide nanomaterials, iron oxide and polymers-based nanoparticles, and
other types of nanoparticles) in the diagnostic and medical purposes have been escalated [4-6].
Carbon nanotubes (CNTs) have attracted tremendous interest in the drug delivery field because of
their unique and promising characteristics including; high surface area to weight ratios, flexible interaction,
reasonable strength, needle-like crystal structures and high loading capacities with cargo drugs, unique
electrical and optical properties, high degrees of stability and biocompatibility, and reversible release of
loaded bioactive cargos at targeted tissue) [7, 8].
İD İD İD