首页> 美国卫生研究院文献>Scientific Reports >Thermodynamic Insights and Conceptual Design of Skin-Sensitive Chitosan Coated Ceramide/PLGA Nanodrug for Regeneration of Stratum Corneum on Atopic Dermatitis
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Thermodynamic Insights and Conceptual Design of Skin-Sensitive Chitosan Coated Ceramide/PLGA Nanodrug for Regeneration of Stratum Corneum on Atopic Dermatitis

机译:皮肤敏感性壳聚糖包覆的神经酰胺/ PLGA纳米药物在特应性皮炎上再生角质层的热力学见解和概念设计。

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摘要

Atopic dermatitis (AD) is a complex skin disease primarily characterized by psoriasis of the stratum corneum. AD drugs have usually been used in acidic and hydrophilic solvents to supply moisture and prevent lipid defects. Ceramide is a typical treatment agent to regenerate the stratum corneum and relieve symptoms of AD. However, ceramide has limitation on direct use for skin because of its low dispersion properties in hydrophilic phase and side effects at excessive treatment. In this study, ceramide imbedded PLGA nanoparticles were developed with chitosan coating (Chi-PLGA/Cer) to overcome this problem. The chitosan coating enhanced initial adherence to the skin and prevented the initial burst of ceramide, but was degraded by the weakly acidic nature of skin, resulting in controlled release of ceramide with additional driving force of the squeezed PLGA nanoparticles. Additionally, the coating kinetics of chitosan were controlled by manipulating the reaction conditions and then mathematically modeled. The Chi-PLGA/Cer was not found to be cytotoxic and ceramide release was controlled by pH, temperature, and chitosan coating. Finally, Chi-PLGA/Cer was demonstrated to be effective at stratum corneum regeneration in a rat AD model. Overall, the results presented herein indicated that Chi-PLGA/Cer is a novel nanodrug for treatment of AD.
机译:特应性皮炎(AD)是一种复杂的皮肤病,主要特征是角质层牛皮癣。通常将AD药物用于酸性和亲水性溶剂中以提供水分并防止脂质缺陷。神经酰胺是一种典型的治疗剂,可再生角质层并缓解AD症状。然而,神经酰胺由于其在亲水相中的低分散性和过度治疗的副作用而在直接用于皮肤方面受到限制。在这项研究中,开发了具有壳聚糖涂层(Chi-PLGA / Cer)的神经酰胺包埋的PLGA纳米颗粒,以解决此问题。壳聚糖涂层增强了对皮肤的初始粘附力并防止了神经酰胺的初始破裂,但是由于皮肤的弱酸性性质而被降解,导致神经酰胺的受控释放以及被挤压的PLGA纳米颗粒的额外驱动力。另外,通过控制反应条件来控制壳聚糖的涂层动力学,然后进行数学建模。未发现Chi-PLGA / Cer具有细胞毒性,并且神经酰胺的释放受pH,温度和壳聚糖涂层的控制。最后,Chi-PLGA / Cer被证明在大鼠AD模型中对角质层再生有效。总体而言,本文呈现的结果表明Chi-PLGA / Cer是用于治疗AD的新型纳米药物。

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