5-Fluorouracil delivery from metal-ion mediated molecularly imprinted cryogel discs

被引:56
作者
Cetin, Kemal [1 ]
Denizli, Adil [1 ]
机构
[1] Hacettepe Univ, Div Biochem, Dept Chem, Ankara, Turkey
关键词
Coordinate bonding; Cryogels; 5-Fluorouracil delivery; Molecular imprinting; 2-HYDROXYETHYL METHACRYLATE HEMA; ANTICANCER DRUG 5-FLUOROURACIL; CONTROLLED-RELEASE; MESOPOROUS SILICA; SUSTAINED-RELEASE; CHELATE AFFINITY; CYTOCHROME-C; COLON-CANCER; IN-VITRO; NANOPARTICLES;
D O I
10.1016/j.colsurfb.2014.12.038
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The objective of this study is to prepare imprinted cryogel discs for delivery of 5-fluorouracil. The coordinate bond interactions are utilized to accomplish a coordination complex between metal-chelate monomer N-methacryloyl-L-histidine and 5-FU with the assistance of Cu2+ ion. The complex is copolymerized with hydroxyethyl methacrylate to produce poly(hydroxyethyl methacrylate-N-methacryloyl-(L)-histidine methyl ester) cryogel discs. The cryogel discs are characterized thoroughly by performing swelling tests, scanning electron microscopy, differential scanning calorimetry and X-ray diffraction studies. In vitro delivery studies are performed to investigate the effects of cross-linker ratio, medium pH and drug concentration. 5-FU imprinted cryogel discs have highly macroporous structures. Drug molecules are homogeneously dispersed in the 5-FU imprinted cryogel matrix. The cumulative release of 5-FU decreased by increasing the cross-linker density in the polymer matrix. Delivery rate of 5-FU varied with different pH values in a coordination complex since metal ion acts as a Lewis acid, and the ligand, i.e. 5-FU acts as a Lewis base. The cumulative release of 5-FU increased with increasing drug concentration in polymer matrix. The nature of the 5-FU transport mechanism is non-Fickian. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:401 / 406
页数:6
相关论文
共 61 条
[1]   Cu(II)-incorporated histidine-containing, magnetic-metal-complexing beads as specific sorbents for the metal chelate affinity of albumin [J].
Akgöl, S ;
Türkmen, D ;
Denizli, A .
JOURNAL OF APPLIED POLYMER SCIENCE, 2004, 93 (06) :2669-2677
[2]   Pharmaceutical applications for molecularly imprinted polymers [J].
Allender, CJ ;
Richardson, C ;
Woodhouse, B ;
Heard, CM ;
Brain, KR .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 195 (1-2) :39-43
[3]   Novel Strategies to Improve the Anticancer Action of 5-Fluorouracil by Using Drug Delivery Systems [J].
Arias, Jose L. .
MOLECULES, 2008, 13 (10) :2340-2369
[4]  
Aydin R.S. Tigli, 2012, J NANOMATER, V2012, P1
[5]   Development of 5-fluorouracil loaded poly(acrylamide-co-methylmethacrylate) novel core-shell microspheres:: In vitro release studies [J].
Babu, V. Ramesh ;
Sairam, Malladi ;
Hosamani, Kallappa M. ;
Aminabhavi, Tejraj M. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 325 (1-2) :55-62
[6]   Injectable preformed scaffolds with shape-memory properties [J].
Bencherif, Sidi A. ;
Sands, R. Warren ;
Bhatta, Deen ;
Arany, Praveen ;
Verbeke, Catia S. ;
Edwards, David A. ;
Mooney, David J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (48) :19590-19595
[7]   Release of 5-fluorouracil from poly(acrylamide-co-monopropyl itaconate) hydrogels [J].
Blanco, TD ;
Garcia, O ;
Olmo, R ;
Teijon, JM ;
Katime, I .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 1996, 680 (1-2) :243-253
[8]   Vascularization of wide pore agarose-gelatin cryogel scaffolds implanted subcutaneously in diabetic and non-diabetic mice [J].
Bloch, K. ;
Vanichkin, A. ;
Damshkaln, L. G. ;
Lozinsky, V. I. ;
Vardi, P. .
ACTA BIOMATERIALIA, 2010, 6 (03) :1200-1205
[9]   Plasma concentrations of 5-fluorouracil and its metabolites in colon cancer patients [J].
Casale, F ;
Canaparo, R ;
Serpe, L ;
Muntoni, E ;
Della Pepa, C ;
Costa, M ;
Mairone, L ;
Zara, GP ;
Fornari, G ;
Eandi, M .
PHARMACOLOGICAL RESEARCH, 2004, 50 (02) :173-179
[10]   Real time in vitro studies of doxorubicin release from PHEMA nanoparticles [J].
Chouhan R. ;
Bajpai A.K. .
J. Nanobiotechnology, 2009, 7 (05) :5