Title of article
Successful Application of Alpha Lipoic Acid Niosomal Formulation in Cerebral Ischemic Reperfusion Injury in Rat Model
Author/Authors
Raeisi Estabragh, Mohammad Amin Pharmaceutics Research Center - Institute of Neuropharmacology - Kerman University of Medical Sciences, Kerman, Iran , Pardakhty, Abbas Pharmaceutics Research Center - Institute of Neuropharmacology - Kerman University of Medical Sciences, Kerman, Iran , Ahmadzadeh, Saeid Pharmaceutical Sciences and Cosmetic Products Research Center - Kerman University of Medical Sciences, Kerman, Iran , Dabiri, Shahriar Pathology and Stem Cell Research Center - Afzalipour Faculty of Medicine - Kerman University of Medical Sciences, Kerman, Iran , Malekpour Afshar, Reza Pathology and Stem Cell Research Center - Afzalipour Faculty of Medicine - Kerman University of Medical Sciences, Kerman, Iran , Farajli Abbasi, Mohammad Neuroscience Research Center - Institute of Neuropharmacology - Kerman University of Medical Sciences, Kerman, Iran
Pages
9
From page
541
To page
549
Abstract
Purpose: Free radicals such as hydroxyl and peroxide are contributing factors to neuronal
destruction in cerebral ischemia. Alpha-lipoic acid (ALA) is one of the potent known
antioxidants. Preparation of ALA niosomes allows IV injection and can increase bioavailability
and penetration into the central nervous system (CNS).
Methods: Film hydration method was used to prepare different niosomes composed of Span®,
Tween®, and cholesterol at different molar ratio. ALA and niosome-forming compounds were
dissolved in chloroform, before removing the organic solvent by rotary evaporator. Animals
were randomly divided into four groups: Sham, control group, intravenous (IV) injection of
empty niosomes plus intraperitoneal (IP) injection of ALA solution, and finally, IV injection
of ALA niosomes. Rats were subjected to deep anesthesia before inducing cerebral ischemia,
then, their internal common carotid arteries were clamped for 15 min and reperfusion was
done for 30 min. Niosomal ALA was injected intravenously just before declamping.
Results: Mean volume diameter of the prepared niosomes was between 4.36 ± 0.82 and 19.95
± 1.21 μm in different formulations. Encapsulation efficiency percent (EE%) of ALA in the
selected formulation, Span60/Tween60/cholesterol (35:35:30 molar ratio), was 94.5 ± 0.2, and
59.27 ± 5.61% of ALA was released after 4h. In the niosomal group, the rate of reduction in
complications of cerebral ischemia such as histopathologic changes and acute damage (from
score 3 to 1) in CNS was higher than other groups.
Conclusion: The obtained results show that niosomes can be used as effective drug delivery
systems for ALA in cerebral ischemia.
Keywords
Niosome , Alpha-lipoic acid , Cerebral ischemia , Antioxidant
Journal title
Advanced Pharmaceutical Bulletin
Serial Year
2022
Record number
2726622
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