Jha Abhishek, Kumar Manish, Goswami Pooja, Manjit Manjit, Bharti Kanchan, Koch Biplob, Mishra Brahmeshwar
Department of Pharmaceutical Engineering & Technology, Indian Institute of Technology (BHU), Varanasi 221005, Uttar Pradesh, India.
Genotoxicology and Cancer Biology Laboratory, Department of Zoology Institute of Science, Banaras Hindu University, Varanasi 221005, Uttar Pradesh, India.
Biomater Adv. 2024 Jun;160:213865. doi: 10.1016/j.bioadv.2024.213865. Epub 2024 Apr 18.
Microneedle technology offers a minimally invasive treatment strategy to deliver chemotherapeutics to localized tumors. Amalgamating the surface functionalized nanoparticles with microneedle technology can potentially deliver drugs directly to tumors and subsequently target cancer cells via, overexpressed receptors on the cell surface, thereby enhancing the treatment efficacy while reducing side effects. Here, we report cetuximab anchored hyaluronic acid-oleylamine and chitosan-oleic acid-based hybrid nanoparticle (HA-OA/CS-OA NPT)-loaded dissolving microneedles (MN) for targeted delivery of cabazitaxel (CBT) in localized breast cancer tumor. The HA-OA/CS-OA NPT was characterized for their size, surface charge, morphology, physicochemical characteristics, drug release behavior, and in vitro anti-cancer efficacy. The HA-OA/CS-OA NPT were of ~125 nm size, showed enhanced cytotoxicity and cellular uptake, and elicited a superior apoptotic response against MDA-MB-231 cells. Subsequently, the morphology and physicochemical characteristics of HA-OA/CS-OA NPT-loaded MN were also evaluated. The fabricated microneedles were of ~550 μm height and showed loading of nanoparticles equivalent to ~250 μg of CBT. The ex vivo skin permeation study revealed fast dissolution of microneedles upon hydration, while the drug permeation across the skin exhibited ~4-fold improvement in comparison to free drug-loaded MN. In vivo studies performed on DMBA-induced breast cancer in female SD rats showed a marked reduction in tumor volume after administration of drug and nanoparticle-loaded microneedles in comparison to intravenous administration of free drug. However, the HA-OA/CS-OA NPT-MN showed the highest tumor reduction and survival rate, with the lowest body weight reduction in comparison to other treatment groups, indicating its superior efficacy and low systemic toxicity. Overall, the dissolving microneedle-mediated delivery of targeted nanoparticles loaded with chemotherapeutics offers a superior alternative to conventional intravenous chemotherapy.
微针技术提供了一种微创治疗策略,可将化疗药物递送至局部肿瘤。将表面功能化的纳米颗粒与微针技术相结合,有可能将药物直接递送至肿瘤,随后通过细胞表面过表达的受体靶向癌细胞,从而提高治疗效果,同时减少副作用。在此,我们报道了负载西妥昔单抗锚定的透明质酸-油胺和壳聚糖-油酸基混合纳米颗粒(HA-OA/CS-OA NPT)的溶蚀性微针(MN),用于在局部乳腺癌肿瘤中靶向递送卡巴他赛(CBT)。对HA-OA/CS-OA NPT的尺寸、表面电荷、形态、理化特性、药物释放行为和体外抗癌疗效进行了表征。HA-OA/CS-OA NPT的尺寸约为125nm,显示出增强的细胞毒性和细胞摄取,并对MDA-MB-231细胞引发了优异的凋亡反应。随后,还评估了负载HA-OA/CS-OA NPT的MN的形态和理化特性。制备的微针高度约为550μm,显示纳米颗粒的负载量相当于约250μg的CBT。体外皮肤渗透研究表明,微针在水化后快速溶解,而与游离药物负载的微针相比,药物透过皮肤的量提高了约4倍。在雌性SD大鼠中对二甲基苯并蒽诱导的乳腺癌进行的体内研究表明,与静脉注射游离药物相比,给药药物和纳米颗粒负载的微针后肿瘤体积显著减小。然而,与其他治疗组相比,HA-OA/CS-OA NPT-MN显示出最高的肿瘤缩小率和生存率,体重减轻最低,表明其具有优异的疗效和低全身毒性。总体而言,负载化疗药物的靶向纳米颗粒的溶蚀性微针介导递送提供了一种优于传统静脉化疗的选择。