Electrospinning of PVA-carboxymethyl cellulose nanofibers for flufenamic acid drug delivery

被引:56
作者
Allafchian, Alireza [1 ,2 ]
Hosseini, Hassan [3 ]
Ghoreishi, Seyyed Mohammad [3 ]
机构
[1] Isfahan Univ Technol, Res Inst Nanotechnol & Adv Mat, Esfahan 8415683111, Iran
[2] Isfahan Univ Technol, Res Inst Biotechnol & Bioengn, Esfahan 8415683111, Iran
[3] Isfahan Univ Technol, Dept Chem Engn, Esfahan 8415683111, Iran
关键词
Drug delivery; Electrospinning; FFA; Carboxymethyl cellulose; MUCILAGE; RELEASE; SYSTEM;
D O I
10.1016/j.ijbiomac.2020.09.129
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A prominent medical application of nanotechnology is represented in drug delivery. In this work, carboxymethyl cellulose (CMC) and poly(vinyl alcohol) (PVA) were used for producing CMC/PVA aqueous-based nanofibers loaded with flufenamic acid (FFA) as a drug containing amine groups. The CMC/PVA solutions with 90/10, 80/20, 70/30, 60/40 and 50/50 ratios were considered for electrospinning. Two integration methods were studied for loading FFA on the nanofibers during the electrospinning process. The characterization techniques of SEM, AFM, fluorescence microscopy and FT-IR spectroscopy were used to study the produced nanofibers, indicating a uniform distribution of FFA throughout the samples. The resulting nanofibers were formed in a diameter range of 176-285 nm and exhibited a 5 h degradation time in the PBS buffer solution. A standard diagram of drug loading was obtained for the samples. The drug release pattern was examined using a dialysis tube method. UV-visible spectroscopy revealed a time-dependent drug release behavior in CMC/PVA/FFA nanofibers where a sharp release occurred over the first 20 min. However, a prolonged release time of 10 h was achieved using a cross-linker (EDC). (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:1780 / 1786
页数:7
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