Preparation and characterization of captopril loaded polycaprolactone electrospun nanofibers
عنوان مقاله: Preparation and characterization of captopril loaded polycaprolactone electrospun nanofibers
شناسه ملی مقاله: JR_NAMJ-10-4_007
منتشر شده در در سال 1402
شناسه ملی مقاله: JR_NAMJ-10-4_007
منتشر شده در در سال 1402
مشخصات نویسندگان مقاله:
Amir Doustgani - Department of Chemical Engineering, Faculty of Engineering, University of Zanjan, Zanjan, Iran
Hossein Allahdinian - Department of Chemistry, Faculty of Science, University of Zanjan, Zanjan, Iran
Ebrahim Ahmadi - Department of Chemistry, Faculty of Science, University of Zanjan, Zanjan, Iran
خلاصه مقاله:
Amir Doustgani - Department of Chemical Engineering, Faculty of Engineering, University of Zanjan, Zanjan, Iran
Hossein Allahdinian - Department of Chemistry, Faculty of Science, University of Zanjan, Zanjan, Iran
Ebrahim Ahmadi - Department of Chemistry, Faculty of Science, University of Zanjan, Zanjan, Iran
Objective(s): Electrospun nanofibrous mats of Polycaprolactone (PCL) and amino modified SBA-۱۵ containing Captopril were prepared and release of drug from prepared nanofibers were investigated in this study.Materials and Methods: Amino modified SBA-۱۵ synthesized through grafting with aminopropyl triethoxy silane. Then, Captopril which is used as an Angiotensin-Converting Enzyme (ACE) inhibitor was loaded as a model drug into the synthesized particles. Furthermore, silica particles containing different amounts of captopril (۷.۵, ۱۰, ۱۵ mg) were loaded into PCL nanofibers’ structure using electrospinning. Therefore, captopril’s release rate in phosphate buffer was analyzed. The analysis of captopril-loaded silica and captopril-loaded nanofibers (without silica) was done in vitro matrix. To identify the acquired nanofibers, FTIR, SEM, SEM mapping, EDX and average diameter calculation were performed. Results: Comparison between the drug release rate of silica-containing nanofibers and bare silica particles indicated that silica particles positively affected the drug release rate. Moreover, kinetic studies have revealed that the drug release rate follows Higuchi and Korsmeyer-Peppas model. Bare nanofibers’ average diameter was ۲۰۹ nm while silica and captopril containing nanofibers were ۲۸۶ nm in average diameter. Conclusion: Therefore, it was concluded that drug-loaded Polycaprolactone nanofibers are potential candidates for biomedical applications.
کلمات کلیدی: Captopril release, Electrospinning, Nanofibers, Nanostructure silica, Polycaprolactone
صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1774653/