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Development and optimization of self-nanoemulsifying drug delivery systems (SNEDDS) for curcumin transdermal delivery: an anti-inflammatory exposure

机译:姜黄素透皮递送的自纳外乳化药物递送系统(SNEDDS)的开发和优化:抗炎暴露

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The purpose of this work is to develop novel lipid-based self-nanoemulsifying drug delivery systems (SNEDDS) as carriers for transdermal delivery of curcumin. SNEDDS containing black seed oil, medium chain mono- and diglycerides and surfactants, were prepared as curcumin delivery vehicles. Their formation spontaneity, morphology, droplet size, and drug loading were evaluated. Gel preparation containing two of the SNEDDS formulations were used in the carrageenan induced paw edema to evaluate the anti-inflammatory effect. Results showed droplet size as low as 71 nm. The highest drug loading was observed with SNEDDS-F6 of ~45mg/g. In In-vivo investigation, SNEDDS-F6 exhibited significant anti-inflammatory activities in terms of 80% reduction in paw edema when compared with positive control. The prepared SNEDDS with the elevated entrapment efficiency, good transdermal penetration ability could be a suitable candidate for effective transdermal curcumin skin delivery.
机译:这项工作的目的是开发新的脂质基自纳乳化药物递送系统(SNEDDS)作为丙锡透皮递送的载体。 含有黑色种子油,中链单 - 和甘油二酯和表面活性剂的鼻涕被制备为姜黄素递送载体。 评估它们的形成自发性,形态,液滴尺寸和药物载荷。 含有两种SnEdds制剂的凝胶制剂用于角叉菜胶诱导的PAW水肿中以评估抗炎作用。 结果显示液滴尺寸低至71nm。 用〜45mg / g的SNEDDS-F6观察到最高药物载量。 在体内调查中,与阳性对照相比,SNEDDS-F6在爪子水肿减少80%的抗炎活动方面表现出显着的抗炎活动。 制备的鼻塞具有升高的血管效率,良好的透皮渗透能力可以是有效透皮姜黄素皮肤递送的合适候选者。

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