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Chitosan-coated liposomes to stabilize and enhance transdermal delivery of indocyanine green for photodynamic therapy of melanoma

机译:壳聚糖涂覆的脂质体稳定和增强吲哚菁绿的透皮递送以进行黑色素瘤的光动力学疗法

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摘要

Indocyanine green (ICG) has been used clinically and noticed as a promising candidate for the topical melanoma photodynamic therapy (PDT). Despite its high potentials in topical PDT, the use of ICG has been hampered by the instability in aqueous solution. In the present study, chitosan-coated liposomes were adopted as a formulation strategy which could stabilize and enhance skin permeation of ICG. Chitosan-coating was verified by the significantly increased liposomal size and reversed zeta potential from negative to positive value by positive chitosan coating. Chitosan-coating liposomes protected ICG from degradation while uncoated liposomes did not. Moreover, they significantly increased cellular uptake and photocytotoxicity of ICG in B16-F10 melanoma cells in a chitosan-dependent manner. The skin permeation of ICG was also drastically improved by chitosan-coated liposomes. These findings emphasize the promising potential of ICG-loaded chitosan-coated liposomes for topical PDT of melanoma.
机译:吲哚菁绿(ICG)已临床使用,并注意到局部黑素瘤光动力治疗(PDT)的有希望的候选者。尽管其局部PDT有很高的潜力,但在水溶液中的不稳定性,使用ICG的使用受到阻碍。在本研究中,采用壳聚糖涂覆的脂质体作为制剂策略,其可稳定和增强ICG的皮肤渗透。通过显着增加的脂质体尺寸和通过阳性壳聚糖涂层从阴性至正值逆转Zeta电位来验证壳聚糖涂层。壳聚糖涂层脂质体保护ICG免于降解,而未涂覆的脂质体没有。此外,它们以壳聚糖依赖性方式显着增加了ICG的植入型ICG的蜂窝摄取和光细胞毒性。通过壳聚糖涂覆的脂质体,ICG的皮肤渗透也急剧改善。这些发现强调了ICG加载的壳聚糖涂层脂质体的有希望的Melanoma局部PDT的潜力。

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