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Microemulsions mediated effective delivery of methotrexate hydrogel: more than a tour de force in psoriasis therapeutics

机译:微乳液介导的甲氨蝶呤水凝胶有效递送:超过牛皮癣治疗剂的旅游力

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Methotrexate (MTX), a well known drug for the treatment of cancer and rheumatoid arthritis, has gained prominence in the treatment of psoriasis over the period of years. However, the present mode of systemic administration through oral or parenteral route has always proposition, full of compromises. The toxicity of drug to the vital organs and physiological environment is the major concern. Also, its poor skin penetration is one major problem. Hence novel system based on lipid carriers has been considered here to overcome the barriers. Microemulsions (MEs) were prepared using pseudo-ternary phase diagram (PTPD) and they were characterized for various parameters such as size, shape (cryo-SEM), PDI, zeta potential, etc. The chosen MEs system (optimized) was then incorporated into secondary vehicles and characterized for rheological behavior, texture profile analysis, in vitro release, ex vivo permeation and drug distribution into different layers of skin. The developed formulations were further evaluated in ex vivo and in vivo such as cell line study, imiquimod-induced psoriatic model, allergic contact dermatitis, rat tail model (% orthokeratosis) and safety test (Draize test). The MEs based MTX gel has shown its potential in locating the drug at the desired domain of stratum corneum, epidermal and dermal layers of skin and reducing systemic absorption. Our results are suggestive of MEs potential as a novel carrier for topical delivery of MTX in topical therapeutic and safety approaches. In conclusion, developed MEs-based hydrogel has shown promising results in achieving effective delivery of MTX.
机译:甲氨蝶呤(MTX)是一种众所周知的用于治疗癌症和类风湿性关节炎的药物,在多年来的治疗中突出了牛皮癣。然而,通过口服或肠胃外途径的全身施用现象始终主张,充满妥协。药物对重要器官和生理环境的毒性是主要关注点。此外,它的皮肤渗透不良是一个主要问题。因此,基于脂质载体的新型系统已经考虑在这里克服屏障。使用伪三元相图(PTPD)制备微乳液(MES),其特征在于各种参数,例如尺寸,形状(Cryo-SEM),PDI,Zeta电位等。然后加入所选择的MES系统(优化)进入二次车辆并表征流变行为,质地谱分析,体外释放,离体渗透和药物分布到不同的皮肤层。在离体和体内进一步评估开发的制剂,如细胞系研究,咪喹莫特诱导的银屑病模型,过敏性接触皮炎,大鼠尾模型(%矫正症)和安全测试(展示试验)。基于MES的MTX凝胶已经示出了在地层角质层,表皮和皮肤层的所需结构域处定位药物并降低全身吸收的可能性。我们的研究结果暗示了MES潜力作为新型载体,用于局部治疗和安全方法中的MTX局部交付。总之,开发的基于MES的水凝胶表明有希望导致达到MTX的有效递送。

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