Development of PCL/PEO electrospun fibrous membranes blended with silane-modified halloysite nanotube as a curcumin release system

被引:58
作者
Bulbul, Y. Emre [1 ]
Okur, Mujgan [2 ]
Demirtas-Korkmaz, Funda [3 ]
Dilsiz, Nursel [1 ,2 ]
机构
[1] Gazi Univ, Grad Sch Nat & Appl Sci, Dept Chem Engn, TR-06570 Ankara, Turkey
[2] Gazi Univ, Fac Engn, Dept Chem Engn, TR-06570 Ankara, Turkey
[3] Gazi Univ, Fac Med, Dept Med Biol & Genet, TR-06570 Ankara, Turkey
关键词
Electrospinning; Halloysite nanotube; Silane modification; Curcumin; Breast cancer; Drug release system; DRUG-DELIVERY SYSTEMS; IN-VITRO; SURFACE MODIFICATION; CLAY NANOTUBES; NANOFIBERS; BIOAVAILABILITY; CELLS; NANOPARTICLES; FABRICATION; FUNCTIONALIZATION;
D O I
10.1016/j.clay.2019.105430
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, electrospun fibrous membranes based on the polycaprolactone (PCL)/polyethylene oxide (PEO) blended with pure, 3-Aminopropyltriethoxysilane (APTES) or 3-Glycidoxypropyltrimethoxysilane (GPTMS) modified halloysite nanotubes (HNT) were prepared by electrospinning for curcumin (Cur) delivery system. The morphological and physicochemical properties of the fabricated membranes were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). In vitro release of from the Cur loaded fibrous membranes was examined in simulated physiological condition by ultraviolet-visible spectroscopy. Besides, in vitro cytotoxicity on the MCF-7 breast carcinoma cells was evaluated. The results demonstrated that the silane-modified HNTs (HNT-APTES and HNT-GPTMS) displayed a much higher Cur loading capacity while APTES modified HNT had the maximum encapsulation efficiency. Moreover, in vitro Cur release studies demonstrated that PCL/PEO-Cur/HNT-APTES membrane has a slower release profile. The release mechanism of Cur from all membranes was fitted by the Peppas-Sahlin kinetic model indicating a pseudo-Fickian and non-Fickian release. Additionally, the PCL/PEO-Cur/HNT-APTES membrane showed the highest toxicity against MCF-7 breast cancer cells. In conclusion, the uses of this Cur loaded PCL/PEO electrospun fibrous membranes blended with the APTES modified HNT can be used to loading of other drugs for controlled drug delivery system, especially as an anticancer carrier.
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页数:14
相关论文
共 119 条
[21]   Dexamethasone loaded core-shell SF/PEO nanofibers via green electrospinning reduced endothelial cells inflammatory damage [J].
Chen, Weiming ;
Li, Dawei ;
EI-Shanshory, Ahmed ;
El-Newehy, Mohamed ;
EI-Hamshary, Hany A. ;
Al-Deyab, Salem S. ;
He, Chuanglong ;
Mo, Xiumei .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2015, 126 :561-568
[22]   Drug delivery systems: Advanced technologies potentially applicable in personalized treatments [J].
Coelho J.F. ;
Ferreira P.C. ;
Alves P. ;
Cordeiro R. ;
Fonseca A.C. ;
Góis J.R. ;
Gil M.H. .
EPMA Journal, 2010, 1 (1) :164-209
[23]   Modeling and comparison of dissolution profiles [J].
Costa, P ;
Manuel, J ;
Lobo, S .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 13 (02) :123-133
[24]  
Dash S, 2010, ACTA POL PHARM, V67, P217
[25]   Polymeric Modification and Its Implication in Drug Delivery: Poly-ε-caprolactone (PCL) as a Model Polymer [J].
Dash, Tapan K. ;
Konkimalla, V. Badireenath .
MOLECULAR PHARMACEUTICS, 2012, 9 (09) :2365-2379
[26]  
Dhawan S., 2005, PHARM TECHNOL, V29, P82
[27]   Chemopreventive and therapeutic effects of curcumin [J].
Duvoix, A ;
Blasius, R ;
Delhalle, S ;
Schnekenburger, M ;
Morceau, F ;
Henry, E ;
Dicato, M ;
Diederich, M .
CANCER LETTERS, 2005, 223 (02) :181-190
[28]   Quercetin-loaded and unloaded electrospun membranes: Synthesis, characterization and in vitro release study [J].
Eskitoros-Togay, S. Melda ;
Bulbul, Y. Emre ;
Dilsiz, Nursel .
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2018, 47 :22-30
[29]   Beaded nanofibers formed during electrospinning [J].
Fong, H ;
Chun, I ;
Reneker, DH .
POLYMER, 1999, 40 (16) :4585-4592
[30]   Electrospinning jets and nanofibrous structures [J].
Garg, Koyal ;
Bowlin, Gary L. .
BIOMICROFLUIDICS, 2011, 5 (01)