Theochari Ioanna, Ilic Tanja, Nicolic Ines, Dobricic Vladimir, Tenchiou Alia, Papahatjis Demetris, Savic Snezana, Xenakis Aristotelis, Papadimitriou Vassiliki, Pletsa Vasiliki
Institute of Chemical Biology, National Hellenic Research Foundation, 48 Vassileos Constantinou Avenue, 11635 Athens, Greece.
Department of Pharmaceutical Technology and Cosmetology, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11221 Belgrade, Serbia.
Biomimetics (Basel). 2021 Jan 27;6(1):10. doi: 10.3390/biomimetics6010010.
During the last decade, many studies have been reported on the design and formulation of novel drug delivery systems proposed for dermal or transdermal administration. The efforts focus on the development of biocompatible nanodispersions that can be delivered to the skin and treat severe skin disorders, including cancer. In this context, oil-in-water (O/W) microemulsions have been developed to encapsulate and deliver lipophilic bioactive molecules for dermal application. An O/W biocompatible microemulsion composed of PBS buffer, Tween 80, and triacetin was assessed for its efficacy as a drug carrier of DPS-2, a lead compound, initially designed in-house to inhibit BRAF oncogenic kinase. The system was evaluated through both in vitro and ex vivo approaches. The cytotoxic effect, in the presence and absence of DPS-2, was examined through the thiazolyl blue tetrazolium bromide (MTT) cell proliferation assay using various cell lines. Further investigation through Western blotting revealed that cells died of necrosis. Porcine ear skin was used as a skin model to evaluate the degree of permeation of DPS-2 through skin and assess its retention. Through the ex vivo experiments, it was clarified that encapsulated DPS-2 was distributed within the full thickness of the stratum corneum (SC) and had a high affinity to hair follicles.
在过去十年中,已有许多关于为皮肤或透皮给药设计和配制新型药物递送系统的研究报道。这些努力集中在开发可递送至皮肤并治疗包括癌症在内的严重皮肤疾病的生物相容性纳米分散体。在此背景下,已开发出水包油(O/W)微乳液来包封和亲脂性生物活性分子用于皮肤应用。评估了一种由磷酸盐缓冲盐水(PBS)缓冲液、吐温80和三醋精组成的O/W生物相容性微乳液作为DPS-2(一种最初在内部设计用于抑制BRAF致癌激酶的先导化合物)药物载体的功效。该系统通过体外和离体方法进行了评估。使用各种细胞系,通过噻唑蓝四唑溴盐(MTT)细胞增殖试验检测了在有无DPS-2情况下的细胞毒性作用。通过蛋白质印迹法的进一步研究表明细胞死于坏死。使用猪耳皮肤作为皮肤模型来评估DPS-2透过皮肤的渗透程度并评估其滞留情况。通过离体实验明确了包封的DPS-2分布在角质层(SC)的全层内,并且对毛囊具有高亲和力。