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Design, preparation and in vitro characterizations of fluconazole loaded nanostructured lipid carriers

机译:氟康唑负载纳米结构脂质载体的设计,制备和体外特征

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Present study was aimed to prepare and characterize fluconazole loaded nanostructured lipid carriers (FLZ-NLCs) for the treatment of fungal infections. Fungal infections are tremendously widespread and are the often faced dermatological condition worldwide. FLZ-NLCs was prepared by ultrasonication emulsion technique using stearic acid (SA) as solid lipid, castor oil as liquid lipid and tween 20 as a surfactant. The mean diameter of optimized FLZ-NLCs were found to be 359.15 ± 9.83 nm. The drug content and entrapment efficiency of NLCs was found to be 102.97 ± 7.45% and 87 ± 0.59%, respectively. In vitro drug release studies of FLZ-NLCs showed 37.34 ± 2.08% drug release over a period of 72 h. The above studies confirmed the prepared FLZ-NLCs may be useful for the treatment of fungal infections.
机译:目前的研究旨在制备和表征氟康唑负载的纳米结构脂质载体(FLZ-NLC)以治疗真菌感染。真菌感染普遍普遍,是全世界经常面临的皮肤病。通过使用硬脂酸(SA)作为固体脂质,蓖麻油作为液体脂质和吐温20作为表面活性剂来制备FLZ-NLC。发现优化的FLZ-NLCs的平均直径为359.15±9.83nm。发现NLC的药物含量和夹带效率分别为102.97±7.45%和87±0.59%。 FLZ-NLC的体外药物释放研究显示,药物释放37.34±2.08%在72小时内。上述研究证实制备的FLZ-NLC可用于治疗真菌感染。

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