Department of Pharmaceutics, Faculty of Pharmacy, Alexandria University, 1 Khartoum Square, Azarita, P.O. Box 21521, Alexandria, Egypt.
Department of Histology and Cell Biology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Drug Deliv Transl Res. 2024 Dec;14(12):3354-3370. doi: 10.1007/s13346-024-01534-9. Epub 2024 Feb 15.
Skin cancer is a widespread type of cancer representing 30% of all cancer types worldwide. Resveratrol (RSV) is an anticancer drug used for skin cancer treatment. Several limitations of RSV such as poor aqueous solubility, first-pass metabolism, and instability limit their topical use. The study aimed to develop and optimize RSV-loaded invasomes for topical administration as well as assess their efficacy in vivo. The optimized RSV-loaded invasomes showed small particle size (208.7 ± 74 nm), PDI (0.3 ± 0.03), high % entrapment efficiency (77.7 ± 6%), and negative zeta potential (-70.4 ± 10.9 mV). They showed an initial burst effect followed by controlled drug release for 24 h. RSV-loaded invasomal gel revealed the highest skin deposition percentage (65%) in ex vivo rat skin, the highest potency (low IC of 6.34 μg/mL), and the highest cellular uptake when tested on squamous cancerous cells (SCCs) when compared to other formulations. The antitumor effect of topical RSV-loaded invasomes was also evaluated in vivo in Ehrlich-induced mice models. The results revealed that RSV-loaded invasomal gel exhibited the smallest tumor volume with no signs of organ toxicity indicating its safety in skin cancer treatment. Upregulation of BAX and Caspase-3 gene levels and downregulation of NF-kB and BCL2 protein levels were demonstrated using RT-PCR and ELISA tests, respectively. Interestingly, the present study is the first to develop RSV-loaded invasomal gel for topical skin cancer treatment. According to our results, invasomes are considered promising lipid-based nanosystems for topical RSV delivery having high skin penetration ability and anticancer effect in the treatment of skin carcinoma.
皮肤癌是一种广泛存在的癌症,占全球所有癌症类型的 30%。白藜芦醇(RSV)是一种用于皮肤癌治疗的抗癌药物。RSV 存在水溶性差、首过代谢和不稳定性等局限性,限制了其局部应用。本研究旨在开发和优化 RSV 负载入侵体用于局部给药,并评估其在体内的疗效。优化的 RSV 负载入侵体显示出较小的粒径(208.7±74nm)、PDI(0.3±0.03)、高包封效率(77.7±6%)和负的 ζ 电位(-70.4±10.9mV)。它们表现出初始突释效应,随后持续 24 小时控制药物释放。与其他制剂相比,RSV 负载入侵体凝胶在离体大鼠皮肤中显示出最高的皮肤沉积百分比(65%)、最高的效力(低 IC 为 6.34μg/mL)和对鳞状癌细胞(SCCs)的最高细胞摄取率。RSV 负载入侵体凝胶的局部抗肿瘤作用也在 Ehrlich 诱导的小鼠模型中进行了体内评价。结果表明,RSV 负载入侵体凝胶表现出最小的肿瘤体积,没有器官毒性的迹象,表明其在皮肤癌治疗中的安全性。使用 RT-PCR 和 ELISA 试验分别证明了 BAX 和 Caspase-3 基因水平的上调和 NF-kB 和 BCL2 蛋白水平的下调。有趣的是,本研究首次开发了 RSV 负载入侵体凝胶用于局部皮肤癌治疗。根据我们的结果,入侵体被认为是有前途的基于脂质的纳米系统,用于局部 RSV 传递,具有高皮肤穿透能力和在治疗皮肤癌中的抗癌作用。