Preparation and Characterization of Chitosan/LDH Composite Membranes for Drug Delivery Application

被引:11
作者
Radu, Elena-Ruxandra [1 ,2 ]
Pandele, Andreea Madalina [2 ]
Tuncel, Cristina [1 ,2 ]
Miculescu, Florin [3 ]
Voicu, Stefan Ioan [1 ,2 ]
机构
[1] Univ Politehn Bucuresti, Fac Chem Engn & Biotechnol, Dept Analyt Chem & Environm Engn, Bucharest 011061, Romania
[2] Univ Politehn Bucuresti, Adv Polymers Mat Grp, Bucharest 011061, Romania
[3] Univ Politehn Bucuresti, Dept Met Mat Sci, Phys Met, 313 Splaiul Independentei, J Bldg, Bucharest 060042, Romania
关键词
LDH; chitosan; composite membranes; diclofenac; drug delivery; CORE-SHELL NANOPARTICLES; DICLOFENAC SODIUM; IN-VITRO; INFRARED-SPECTROSCOPY; CONTROLLED-RELEASE; TARGETED DELIVERY; DEACETYLATION; EFFICIENT; CELLULOSE; BARRIER;
D O I
10.3390/membranes13020179
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
In this study, composite membranes based on chitosan (CS), layered double hydroxide (LDH), and diclofenac were prepared via dispersing of LDH and diclofenac (DCF) in the chitosan matrix for gradual delivery of diclofenac sodium. The effect of using LDH in composites was compared to chitosan loaded with diclofenac membrane. LDH was added in order to develop a system with a long release of diclofenac sodium, which is used in inflammatory conditions as an anti-inflammatory drug. The prepared composite membranes were characterized by Fourier Transform Infrared Spectroscopy (FT-IR), Scanning Electron Microscope Analysis (SEM), X-ray Photoelectron Spectroscopy (XPS), Thermogravimetric Analysis (TGA) and UV-Vis Spectroscopy. The results of the FTIR and XPS analyses confirmed the obtaining of the composite membrane and the efficient incorporation of diclofenac. It was observed that the addition of LDH can increase the thermal stability of the composite membrane and favors the gradual release of diclofenac, highlighted by UV-Vis spectra that showed a gradual release in the first 48 h. In conclusion, the composite membrane based on CS-LDH can be used in potential drug delivery application.
引用
收藏
页数:14
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