Volume 35, Issue 6 (September 2024)                   Studies in Medical Sciences 2024, 35(6): 492-501 | Back to browse issues page

Ethics code: IR.UMSU.REC.1398.416


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Azemoodeh M, Shirpoor A, Rasmi Y, Fathi Azarbayjani A. DEVELOPMENT AND EVALUATION OF NOVEL PIOGLITAZONE DRUG DELIVERY SYSTEM IN DIABETIC WISTAR RAT MODEL. Studies in Medical Sciences 2024; 35 (6) :492-501
URL: http://umj.umsu.ac.ir/article-1-6256-en.html
Urmia University of Medical Sciences , anahita@u.nus.edu
Abstract:   (182 Views)
Abstract
Background & Aims: Diabetes is a metabolic disorder characterized by high blood glucose levels and insulin resistance. Pioglitazone can lower insulin resistance and has anti-inflammatory properties. The aim of this work was to develop pioglitazone-loaded nanofibers and to evaluate their effect as a dermal implant device to lower blood glucose levels. The effect of pioglitazone-loaded nanofiber was investigated as a wound dressing in diabetic Wistar rats.
 Materials & Methods: In this work, nanofibers were developed using the electrospinning method. The structure and characteristics of the fibers were evaluated using scanning electron microscopy and Fourier Transform Infrared Spectroscopy. The effect of nanofiber implants was evaluated on blood glucose levels , and their wound healing effect was investigated in diabetic wounds in a Wistar rat model.
Results: The developed formulations did not show any effect in lowering blood glucose when used as an implant; however, they were able to accelerate the wound healing rate when used as a dressing in the wound model. This effect might be due to the anti-inflammatory properties of the drug. The developed wound dressing was able to accelerate the formation of the epidermis and dermis layers in the wound model.
Conclusion: Histological studies indicate that wounds treated with pioglitazone-loaded nanofibers exhibit an anti-inflammatory effect and therefore can increase the wound healing rate. These drug-loaded nanofibers enhanced the development of collagen and improved the formation of the epidermis and dermis while reducing the number of inflammatory cells. The developed drug delivery system was not able to significantly decrease blood glucose levels in the animal model. This effect may be due to the low drug loading capacity as well as its poor aqueous solubility.
 

 
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Type of Study: Research | Subject: فارماکولوژی

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