Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Department of Pharmacognosy, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Drug Dev Res. 2023 Nov;84(7):1453-1467. doi: 10.1002/ddr.22097. Epub 2023 Jul 30.
Breast cancer represents a life-threatening problem globally. The major challenge in the clinical setting is the management of cancer resistance and metastasis. Hybrid therapy can affect several cellular targets involved in carcinogenesis with a lessening of adverse effects. Therefore, the current study aims to assemble, and optimize a hybrid of gefitinib (GFT) and simvastatin (SIM)-loaded nanostructured lipid carrier (GFT/SIM-NLC) to combat metastatic and drug-resistant breast cancer. GFT/SIM-NLC cargos were prepared using design of experiments to investigate the impact of poloxamer-188 and fatty acids concentrations on the physicochemical and pharmaceutical behavior properties of NLC. Additionally, the biosafety of the prepared GFT/SIM-NLC was studied using a fresh blood sample. Afterward, the optimized formulation was subjected to an MTT assay to study the cytotoxic activity of GFT/SIM-NLC compared to free GFT/SIM using an MCF-7 cell line as a surrogate model for breast cancer. The present results revealed that the particle size of the prepared NLC ranged from (209 to 410 nm) with a negative zeta potential value ranging from (-17.2 to -23.9 mV). Moreover, the optimized GFT/SIM-NLC formulation showed favorable physicochemical properties and promising lymphatic delivery cargos. A biosafety study indicates that the prepared NLC has a gentle effect on erythrocyte hemolysis. Cytotoxicity studies revealed that GFT/SIM-NLC enhanced the killing of the MCF-7 cell line compared to free GFT/SIM. This study concluded that the hybrid therapy of GFT/SIM-NLC is a potential approach to combat metastatic and drug-resistant breast cancer.
乳腺癌是全球性的危及生命的问题。临床面临的主要挑战是癌症耐药性和转移的管理。联合治疗可以影响致癌作用中涉及的几个细胞靶标,同时减少不良反应。因此,本研究旨在组装和优化吉非替尼(GFT)和辛伐他汀(SIM)负载的纳米结构脂质载体(GFT/SIM-NLC)的混合物,以对抗转移性和耐药性乳腺癌。使用实验设计制备 GFT/SIM-NLC 载体,以研究泊洛沙姆 188 和脂肪酸浓度对 NLC 的物理化学和药物行为特性的影响。此外,使用新鲜血样研究了制备的 GFT/SIM-NLC 的生物安全性。然后,将优化的配方进行 MTT 测定,以研究 MCF-7 细胞系作为乳腺癌替代模型的 GFT/SIM-NLC 与游离 GFT/SIM 的细胞毒性活性。目前的结果表明,所制备的 NLC 的粒径范围为(209 至 410nm),具有负的 Zeta 电位值范围为(-17.2 至-23.9mV)。此外,优化的 GFT/SIM-NLC 配方表现出良好的物理化学性质和有前途的淋巴递药载体。生物安全性研究表明,所制备的 NLC 对红细胞溶血具有温和的影响。细胞毒性研究表明,与游离 GFT/SIM 相比,GFT/SIM-NLC 增强了 MCF-7 细胞系的杀伤作用。本研究得出结论,GFT/SIM-NLC 的联合治疗是一种对抗转移性和耐药性乳腺癌的潜在方法。