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首页> 外文期刊>Saudi Pharmaceutical Journal >Transdermal patches loaded with L-cysteine HCL as a strategy for protection from mobile phone emitting electromagnetic radiation hazards
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Transdermal patches loaded with L-cysteine HCL as a strategy for protection from mobile phone emitting electromagnetic radiation hazards

机译:载有L-半胱氨酸盐酸盐的透皮贴剂可作为防止手机发出电磁辐射危害的策略

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Mobile phone usage has been increased in the last few years emitting electromagnetic radiation (EMR), which disturbs normal cellular processes via oxidative stress. L-cysteine, a glutathione precursor, prevents oxidative damage. Transdermal patches (TDPs) loaded with L-cysteine hydrochloride (L-CyS-HCL) were fabricated by dispersion of L-CyS-HCL 5% w/w and different concentrations of sorbitol as a plasticizer in room-temperature vulcanizable synthetic silicone matrices (RTV-Si). The effect of sorbitol on patch physicochemical parameters was assessed; in-vitro L-CyS-HCL release profiles and ex-vivo permeation were studied. Pharmacokinetic parameters of endogenous synthetized in-vivo glutathione, after receiving IV bolus dose of L-CyS-HCl and L-CyS-HCl-RTV-Si-TDPs were studied in rat model. The influence of L-CyS-HCL-RTV-Si-TDPs against damaging effects of mobile phone EMR on rats' blood and brain tissues was studied. The results revealed that patch plasticity, intensity reflections, surface porosity, L-CyS-HCL release rate and skin permeation increased with increasing sorbitol concentration. Pharmacokinetic profile for IV dose and L-CyS-HCl-RTV-Si-TDPs revealed that the L-CyS-HCl-RTV-Si-TDPs provided a sustained glutathione plasma concentration–time profile over entire patch application. High significant differences in biological parameters (blood and brain samples) were observed for radiated rats using the patch in study compared with positive control rats. Promising long-term strategy for protection against mobile phone hazards was obtained.
机译:在最近几年中,移动电话的使用有所增加,它会发出电磁辐射(EMR),这会通过氧化应激干扰正常的细胞过程。 L-半胱氨酸是谷胱甘肽的前体,可防止氧化损伤。负载L-半胱氨酸盐酸盐(L-CyS-HCL)的透皮贴剂(TDP)是通过将5%w / w的L-CyS-HCL和不同浓度的山梨醇作为增塑剂分散在室温可硫化合成有机硅基质中制成的( RTV-Si)。评估了山梨糖醇对贴剂理化参数的影响;研究了体外L-CyS-HCL释放曲线和离体渗透。在大鼠模型中,研究了内源性合成的体内谷胱甘肽的药代动力学参数,在接受静脉推注剂量的L-CyS-HCl和L-CyS-HCl-RTV-Si-TDP后。研究了L-CyS-HCL-RTV-Si-TDPs对手机EMR对大鼠血液和脑组织的破坏作用的影响。结果表明,随着山梨糖醇浓度的增加,斑块的可塑性,强度反射,表面孔隙率,L-CyS-HCL释放速率和皮肤渗透性增加。 IV剂量和L-CyS-HCl-RTV-Si-TDPs的药代动力学曲线显示,在整个贴剂应用中,L-CyS-HCl-RTV-Si-TDPs提供了持续的谷胱甘肽血浆浓度-时间曲线。与阳性对照大鼠相比,使用研究中的贴片对放疗的大鼠观察到生物学参数(血液和脑样本)的高度显着差异。获得了防止手机危险的有希望的长期策略。

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