Alginate nanoparticles protect ferrous from oxidation: Potential iron delivery system

被引:67
作者
Katuwavila, Nuwanthi P. [1 ,3 ]
Perera, A. D. L. C. [1 ,2 ]
Dahanayake, Damayanthi [3 ]
Karunaratne, V. [2 ,3 ]
Amaratunga, Gehan A. J. [3 ,4 ]
Karunaratne, D. Nedra [1 ,2 ]
机构
[1] Univ Peradeniya, Post Grad Inst Sci, Peradeniya, Sri Lanka
[2] Univ Peradeniya, Dept Chem, Fac Sci, Peradeniya, Sri Lanka
[3] SriLanka Inst Nanotechnol, Pitipana, Homagama, Sri Lanka
[4] Univ Cambridge, Elect Engn Div, Dept Engn, 9 JJ Thomson Ave, Cambridge CB3 0FA, England
关键词
Anemia; Ferrous sulfate; Alginate nanoparticles; Iron loaded nanocomposite; Bioavailability; FORTIFICATION; DEFICIENCY;
D O I
10.1016/j.ijpharm.2016.09.053
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A novel, efficient delivery system for iron (Fe2+) was developed using the alginate biopolymer. Iron loaded alginate nanoparticles were synthesized by a controlled ionic gelation method and was characterized with respect to particle size, zeta potential, morphology and encapsulation efficiency. Successful loading was confirmed with Fourier Transform Infrared spectroscopy and Thermogravimetric Analysis. Electron energy loss spectroscopy study corroborated the loading of ferrous into the alginate nanoparticles. Iron encapsulation (70%) was optimized at 0.06% Fe (w/v) leading to the formation of iron loaded alginate nanoparticles with a size range of 15-30 nm and with a negative zeta potential (-38 mV). The in vitro release studies showed a prolonged release profile for 96 h. Release of iron was around 65-70% at pH of 6 and 7.4 whereas it was less than 20% at pH 2. The initial burst release upto 8 h followed zero order kinetics at all three pH values. All the release profiles beyond 8 h best fitted the Korsmeyer-Peppas model of diffusion. Non Fickian diffusion was observed at pH 6 and 7.4 while at pH 2 Fickian diffusion was observed. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:404 / 409
页数:6
相关论文
共 31 条
[1]  
Abbaspour N, 2014, J RES MED SCI, V19, P164
[2]  
Aynie I., 2009, ANTISENSE NUCLEIC A, V9, P301
[3]   Hepcidin levels predict nonresponsiveness to oral iron therapy in patients with iron deficiency anemia [J].
Bregman, David B. ;
Morris, David ;
Koch, Todd A. ;
He, Andy ;
Goodnough, Lawrence T. .
AMERICAN JOURNAL OF HEMATOLOGY, 2013, 88 (02) :97-101
[4]   IRON FORTIFICATION - AN UPDATE [J].
COOK, JD ;
REUSSER, ME .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1983, 38 (04) :648-659
[5]   Synthesis and characterization of calcium alginate nanoparticles, sodium homopolymannuronate salt and its calcium nanoparticles [J].
Daemi, H. ;
Barikani, M. .
SCIENTIA IRANICA, 2012, 19 (06) :2023-2028
[6]   Chemical, physical and biological properties of alginates and their biomedical implications [J].
Draget, Kurt I. ;
Taylor, Catherine .
FOOD HYDROCOLLOIDS, 2011, 25 (02) :251-256
[7]   Electron energy-loss spectroscopy in the TEM [J].
Egerton, R. F. .
REPORTS ON PROGRESS IN PHYSICS, 2009, 72 (01)
[8]   Iron fortification in dairy industry [J].
Gaucheron, F .
TRENDS IN FOOD SCIENCE & TECHNOLOGY, 2000, 11 (11) :403-409
[9]   Calcium alginate nanocarriers as possible vehicles for oral delivery of insulin [J].
Goswami, Shilpi ;
Bajpai, Jaya ;
Bajpai, A. K. .
JOURNAL OF EXPERIMENTAL NANOSCIENCE, 2014, 9 (04) :337-356
[10]   Mathematical modeling of simultaneous drug release and in vivo absorption [J].
Grassi, Mario ;
Lamberti, Gaetano ;
Cascone, Sara ;
Grassi, Gabriele .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 418 (01) :130-141