Preparation and characterization of naftifine-loaded poly(vinyl alcohol)/sodium alginate electrospun nanofibers

被引:3
|
作者
Esenturk, Imren [1 ,4 ]
Balkan, Timucin [2 ,3 ,5 ]
Gungor, Sevgi [1 ]
Sarac, Sezai [2 ,3 ]
Erdal, Meryem Sedef [1 ]
机构
[1] Istanbul Univ, Fac Pharm, Dept Pharmaceut Technol, TR-34116 Istanbul, Turkey
[2] Istanbul Tech Univ, Polymer Sci & Technol, Istanbul, Turkey
[3] Istanbul Tech Univ, Nanosci & Nanoengn, Istanbul, Turkey
[4] Univ Hlth Sci Turkey, Fac Pharm, Dept Pharmaceut Technol, Istanbul, Turkey
[5] Koc Univ, TUPRAS Energy Ctr KUTEM, Istanbul, Turkey
关键词
Naftifine; Nanofibers; Electrospinning; Topical drug delivery; COMPOSITE NANOFIBERS; IN-VITRO; DELIVERY; RELEASE; COMPLEXES; ALCOHOL; DESIGN; DRUGS; MATS;
D O I
10.1590/s2175-97902019000318440
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, naftifine (a topical antifungal drug) loaded poly(vinyl) alcohol (PVA)/sodium alginate (SA) nanofibrous mats were prepared using the single-needle electrospinning technique. The produced nanofibers were crosslinked with glutaraldehyde (GTA) vapor. The morphology and diameter of the electrospun nanofibers were studied by scanning electron microscopy (SEM). SEM images showed the smoothness of the nanofibers and indicated that the fiber diameter increased with crosslinking and drug loading. Atomic force microscopy (AFM) images confirmed the uniform production of the scaffolds, and elemental mapping via energy dispersive X-ray spectroscopy (EDS) showed the uniform distribution of the drug within the nanofibers. An attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy study demonstrated that naftifine has sufficient secondary interactions with the polymer blend. The crosslinking treatment decreased the burst drug release effectively and the release mechanism followed Korsmeyer-Peppas Super Case-II transport. Overall, these findings suggest the potential use of naftifine-loaded PVA/SA nanofibers as a topical antifungal drug delivery system.
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页数:12
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