Medical Bionanotechnology, Faculty of Allied Health Sciences, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Chettinad Health City, Kelambakkam, Chennai 603103, India.
Molecules. 2024 Apr 30;29(9):2077. doi: 10.3390/molecules29092077.
Cancer is one of the major causes of death, and its negative impact continues to rise globally. Chemotherapy, which is the most common therapy, has several limitations due to its tremendous side effects. Therefore, developing an alternate therapeutic agent with high biocompatibility is indeed needed. The anti-oxidative effects and bioactivities of several different crude extracts of marine algae have been evaluated both in vitro and in vivo. In the present study, we synthesized the aqueous extract (HA) from the marine algae , and then, a liposome was formulated for that extract (NHA). The extracts were characterized using different photophysical tools like dynamic light scattering, UV-visible spectroscopy, FTIR, scanning electron microscopy, and GC-MS analysis. The SEM image revealed a size range of 112-185 nm for NHA and the GC-MS results showed the presence of octadecanoic acid and n-Hexadecanoic acid in the majority. The anticancer activity was studied using A549 cells, and the NHA inhibited the cancer cells dose-dependently, with the highest killing of 92% at 100 μg/mL. The in vivo studies in the zebrafish model showed that neither the HA nor NHA of showed any teratogenic effect. The outcome of our study showed that NHA can be a potential drug candidate for inhibiting cancer with good biocompatibility up to a dose of 100 μg/mL.
癌症是主要死因之一,其负面影响在全球范围内持续上升。化疗是最常见的治疗方法,但由于其巨大的副作用,存在一些局限性。因此,确实需要开发一种具有高生物相容性的替代治疗剂。已经评估了几种不同海洋藻类的粗提取物的抗氧化作用和生物活性,无论是在体外还是在体内。在本研究中,我们合成了海洋藻类的水提取物(HA),然后为该提取物(NHA)配制了脂质体。使用不同的光物理工具,如动态光散射、紫外可见光谱、傅里叶变换红外光谱、扫描电子显微镜和 GC-MS 分析对提取物进行了表征。SEM 图像显示 NHA 的尺寸范围为 112-185nm,GC-MS 结果表明,在大多数情况下,存在十八烷酸和正十六烷酸。使用 A549 细胞研究了抗癌活性,NHA 剂量依赖性地抑制癌细胞,在 100μg/mL 时最高杀伤率为 92%。在斑马鱼模型中的体内研究表明,HA 和 的 NHA 均未显示出任何致畸作用。我们的研究结果表明,NHA 可以成为一种具有良好生物相容性的潜在候选药物,其抑制癌症的有效剂量高达 100μg/mL。