Padya Bharath Singh, Fernandes Gasper, Hegde Sumukha, Kulkarni Sanjay, Pandey Abhijeet, Deshpande Praful Balavant, Ahmad Sheikh F, Upadhya Dinesh, Mutalik Srinivas
Department of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal 576104, Karnataka, India.
Department of Pharmaceutics Sciences, Vignan Foundation for Science, Technology and Research, Vadlamudi, Guntur 522213, Andhra Pradesh, India.
Pharmaceutics. 2023 Nov 7;15(11):2594. doi: 10.3390/pharmaceutics15112594.
The therapeutic effectiveness of the most widely used anticancer drug 5-fluorouracil (5-FU) is constrained by its high metabolism, short half-life, and rapid drug resistance after chemotherapy. Although various nanodrug delivery systems have been reported for skin cancer therapy, their retention, penetration and targeting are still a matter of concern. Hence, in the current study, a topical gel formulation that contains a metal-organic framework (zeolitic imidazole framework; ZIF-8) loaded with 5-FU and a surface modified with sonidegib (SDG; acting as a therapeutic agent as well as a targeting ligand) (5-FU@ZIF-8 MOFs) is developed against DMBA-UV-induced BCC skin cancer in rats. The MOFs were prepared using one-pot synthesis followed by post drug loading and SDG conjugation. The optimized MOFs were incorporated into hyaluronic acid-hydroxypropyl methyl cellulose gel and further subjected to characterization. Enhanced skin deposition of the 5-FU@ZIF-8-SDG MOFs was observed using ex vivo skin permeation studies. Confocal laser microscopy studies showed that 5-FU@ZIF-8-SDG MOFs permeated the skin via the transfollicular pathway. The 5-FU@ZIF-8-SDG MOFs showed stronger cell growth inhibition in A431 cells and good biocompatibility with HaCaT cells. Histopathological studies showed that the efficacy of the optimized MOF gels improved as the epithelial cells manifested modest hyperplasia, nuclear pleomorphism, and dyskeratosis. Additionally, immunohistochemistry and protein expression studies demonstrated the improved effectiveness of the 5-FU@ZIF-8-SDG MOFs, which displayed a considerable reduction in the expression of Bcl-2 protein. Overall, the developed MOF gels showed good potential for the targeted delivery of multifunctional MOFs in topical formulations for treating BCC cancer.
最广泛使用的抗癌药物5-氟尿嘧啶(5-FU)的治疗效果受到其高代谢率、短半衰期以及化疗后迅速产生耐药性的限制。尽管已有多种纳米药物递送系统用于皮肤癌治疗,但其滞留、渗透和靶向性仍是令人关注的问题。因此,在本研究中,开发了一种局部凝胶制剂,其包含负载有5-FU的金属有机框架(沸石咪唑框架;ZIF-8)且表面用索尼吉布(SDG;既是治疗剂又是靶向配体)修饰(5-FU@ZIF-8 MOFs),用于对抗二甲基苯并蒽(DMBA)-紫外线诱导的大鼠基底细胞癌(BCC)皮肤癌。MOFs采用一锅法合成,随后进行药物负载和SDG偶联。将优化后的MOFs掺入透明质酸-羟丙基甲基纤维素凝胶中,并进一步进行表征。通过体外皮肤渗透研究观察到5-FU@ZIF-8-SDG MOFs在皮肤中的沉积增强。共聚焦激光显微镜研究表明,5-FU@ZIF-8-SDG MOFs通过毛囊途径渗透皮肤。5-FU@ZIF-8-SDG MOFs在A431细胞中显示出更强的细胞生长抑制作用,并且与HaCaT细胞具有良好的生物相容性。组织病理学研究表明,随着上皮细胞出现轻度增生、核异形性和角化异常,优化后的MOF凝胶的疗效有所提高。此外,免疫组织化学和蛋白质表达研究证明了5-FU@ZIF-8-SDG MOFs的有效性提高,其显示Bcl-2蛋白的表达显著降低。总体而言,所开发的MOF凝胶在用于治疗BCC癌症的局部制剂中显示出用于多功能MOFs靶向递送的良好潜力。