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首页> 外文期刊>International Journal of Pharmaceutics >Ex vivo skin permeation and retention studies on chitosan-ibuprofen-gellan ternary nanogel prepared by in situ ionic gelation technique-a tool for controlled transdermal delivery of ibuprofen
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Ex vivo skin permeation and retention studies on chitosan-ibuprofen-gellan ternary nanogel prepared by in situ ionic gelation technique-a tool for controlled transdermal delivery of ibuprofen

机译:原位离子凝胶技术制备的壳聚糖-布洛芬-吉兰三元纳米凝胶的离体皮肤渗透和保留研究-布洛芬可控透皮递送工具

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The chemical potentials of drug-polymer electrostatic interaction have been utilized to develop a novel ternary chitosan-ibuprofen-gellan nanogel as controlled transdermal delivery tool for ibuprofen. The ternary nanogels were prepared by a combination of electrostatic nanoassembly and ionic gelation techniques. The electrostatic and hydrophobic interactions as well as hydrogen bonding between ibuprofen and chitosan were confirmed with FTIR, while DSC, TGA and SEM confirmed the physical state, thermal and morphological characteristics, respectively. The ex vivo delivery of ibuprofen onto and across the skin was evaluated based on system specific drug release parameters such as steady state permeation rate, permeability coefficient, permeability enhancement ratio, skin/gel partition coefficient, diffusion coefficient, lag time and release rate constant and mechanisms of release were determined using mathematical models. Interaction between ibuprofen and chitosan produced new spherical eutectic nanoconjugates with remarkable decrease in particle size of ibuprofen from 4580 (length-to-breadth aspect ratio) to a minimum of 14.15 nm (324-times), and thermally stable amorphous characteristics. The nanogels exhibited significant elastic and pseudoplastic characteristics dictated by the concentration of chitosan with maximum swelling capacity of 775% w/w at 6.55 mM chitosan compared with 281.16 and 506.50% for plain gellan and control ibuprofen hydrogel, respectively. Chitosan enhanced the skin penetration, permeability and the rate of transdermal release of ibuprofen by a factor of 4, dictated by the extent of ibuprofen-chitosan ionic interaction and its concentration. The major mechanism of ibuprofen release through the pig skin was drug diffusion however drug partition and matrix erosion also occurred. It was evident that ternary nanogels are novel formulations with potential application in controlled transdermal delivery of ibuprofen. (C) 2015 Elsevier B.V. All rights reserved.
机译:药物-聚合物静电相互作用的化学势已被用于开发一种新型的壳聚糖-布洛芬-吉兰三元纳米凝胶,作为布洛芬的受控透皮递送工具。通过结合静电纳米组装和离子凝胶技术制备三元纳米凝胶。 FTIR证实了布洛芬与壳聚糖之间的静电和疏水相互作用以及氢键,而DSC,TGA和SEM分别证实了其物理状态,热学和形态学特征。根据系统特定的药物释放参数,如稳态渗透率,渗透系数,渗透率增强比,皮肤/凝胶分配系数,扩散系数,滞后时间和释放速率常数,评估布洛芬在皮肤上和在皮肤上的离体递送。使用数学模型确定释放机理。布洛芬和壳聚糖之间的相互作用产生了新的球形共晶纳米共轭物,布洛芬的粒径从4580(长宽比)显着减小到最小14.15 nm(324倍),并且具有热稳定的非晶态特性。纳米凝胶显示出显着的弹性和假塑性特征,这是由壳聚糖的浓度决定的,壳聚糖在6.55 mM时的最大溶胀能力为775%w / w,而普通吉兰糖凝胶和对照布洛芬水凝胶分别为281.16和506.50%。壳聚糖将布洛芬-壳聚糖离子相互作用的程度和浓度决定了皮肤渗透性,通透性和布洛芬透皮释放速率提高了4倍。布洛芬通过猪皮释放的主要机理是药物扩散,但是也发生了药物分配和基质侵蚀。显然,三元纳米凝胶是新颖的制剂,在布洛芬的受控透皮递送中具有潜在的应用。 (C)2015 Elsevier B.V.保留所有权利。

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