Badr-Eldin Shaimaa M, Aldawsari Hibah M, Alhakamy Nabil A, Fahmy Usama A, Ahmed Osama A A, Neamatallah Thikryat, Tima Singkome, Almaghrabi Raghad H, Alkudsi Fayda M, Alamoudi Asmaa A, Alzahrani Amjad A, Kotta Sabna, Al-Hejaili Omar D
Department of Pharmaceutics, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Center of Excellence for Drug Research and Pharmaceutical Industries, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Pharmaceutics. 2022 May 9;14(5):1024. doi: 10.3390/pharmaceutics14051024.
Simvastatin (SMV) is an antihyperlipidemic agent that has been investigated as a possible anti-cancer agent. An obstacle to malignant tumor therapy using drugs is the delivery of adequate levels to the cancer cells while minimizing side effects following their systemic administration. To circumvent this challenge, the researchers directed towards the field of nanotechnology to benefit from the nano-size of the formulation in passively targeting the tumor cells. Thus, our study aimed at investigating the potential of a combined mixture-process variable design for optimization of SMV spanlastics (SMV-SPNs) with minimized particle size and maximized zeta potential to enhance the anticancer activity of the drug. The study investigated the effects of Span 20 and Tween 80 as mixture components and sonication time as a process variable on particle size, polydispersity index, and zeta potential as responses. SPNs were prepared using an ethanol injection method. Combining the predicted optimized variables' levels is supposed to achieve the set goals with a desirability of 0.821. The optimized spanlastics exhibited a measured globule size of 128.50 nm, PDI of 0.329, and ZP of -29.11 mV. The percentage relative error between predicted responses and the observed ones were less than 5% for the three responses, indicating the optimization technique credibility. A significant improvement in the cytotoxicity of the optimized formulation against three different cancerous cell lines was observed in comparison with SMV. The inhibitory concentration (IC) values of MCF-7, HCT-116, and HEPG2 were found to be 0.89, 0.39, and 0.06 μM at 24 h incubation. The enhanced cytotoxicity could be assigned to the possible improved permeation and preferential build-up within the cancerous cells by virtue of the minimized size. These findings imply that SMV-SPNs could be an ideal strategy to combat cancer.
辛伐他汀(SMV)是一种抗高血脂药物,已被作为一种可能的抗癌药物进行研究。使用药物进行恶性肿瘤治疗的一个障碍是在全身给药时,要在将足够剂量的药物输送到癌细胞的同时,尽量减少副作用。为了克服这一挑战,研究人员转向纳米技术领域,以利用制剂的纳米尺寸来被动靶向肿瘤细胞。因此,我们的研究旨在探讨一种组合混合 - 工艺变量设计的潜力,以优化辛伐他汀弹性体纳米粒(SMV - SPNs),使其粒径最小化且zeta电位最大化,从而增强药物的抗癌活性。该研究考察了Span 20和吐温80作为混合成分以及超声处理时间作为工艺变量对粒径、多分散指数和zeta电位的影响,并将其作为响应指标。采用乙醇注入法制备SPNs。将预测的优化变量水平相结合,有望以0.821的期望度实现设定目标。优化后的弹性体纳米粒的实测球粒尺寸为128.50 nm,多分散指数为0.329,zeta电位为 - 29.11 mV。对于这三个响应指标,预测响应与观察响应之间的相对误差百分比均小于5%,表明优化技术的可信度。与SMV相比,观察到优化后的制剂对三种不同癌细胞系的细胞毒性有显著改善。在孵育24小时时,MCF - 7、HCT - 116和HEPG2的抑制浓度(IC)值分别为0.89、0.39和0.06 μM。增强的细胞毒性可能归因于粒径最小化使得药物在癌细胞内的渗透可能得到改善以及优先聚集。这些发现表明,SMV - SPNs可能是对抗癌症的理想策略。