Dubey Swati, Virmani Tarun, Yadav Shiv Kumar, Kumar Girish, Sharma Ashwani, Gugulothu Dalapathi
Department of Pharmacy, School of Pharmaceutical Sciences, MVN University, Palwal, Haryana, India.
Department of Pharmacy, B.S. Anangpuria Institute of Pharmacy, Faridabad, India.
Curr Pharm Des. 2025;31(16):1270-1289. doi: 10.2174/0113816128329342241120105041.
BACKGROUND: The metal oxide nanoparticles possess unique properties such as biological compatibility, superior reactivity, and capacity to develop reactive oxygen species, due to this they have drawn significant interest in cancer treatment. The various MONPs such as Cerium oxide, Copper oxide, Iron oxide, Titanium dioxide, and Zinc oxide have been investigated for several types of cancers including brain, breast, cervical, colon, leukemia, liver, lung, melanoma, ovarian, and prostate cancers. However, traditional physiochemical synthetic methods for MONPs commonly include toxic materials, a major concern that raises questions regarding their biocompatibility and safety. OBJECTIVE: This study aims to investigate the role of plant phytoconstituents in the development of MONPs via green synthesis and explore the therapeutic effectiveness of MONPs in treating several types of cancer. Primarily, it examines the potential of plant phytoconstituents (phenolic compounds, flavonoids, glycosides, alkaloids, etc.) in the development of MONPs as well as their improved ability to target numerous types of cancer. METHODS: A systemic search was conducted on recent literature, focusing on developing green MONPs by utilizing plants' phytoconstituents (plant extracts). The study of plant phytochemicals (present in different parts of a plant such as leaves, flowers, stems, peels, and roots) and their role in the synthesis of green metal oxide nanoparticles as well as their anticancer activity against several types of cancers was analyzed. Also focusing on their anticancer mechanism that involves ROS production, generates oxidative stress, and apoptosis leads to cancer inhibition. RESULTS: Phytochemicals-mediated metal oxide nanoparticle synthesis revealed many advantages such as improved biological compatibility and enhanced sensitivity towards cancer cells. Phytochemicals present in plant extracts act as natural capping, reducing, and stabilizing agents, enhancing nanoparticle synthesis which leads to synergistic anticancer activity. Additionally, the natural antioxidant and anticancer activity of various phytochemicals enhances the therapeutic potential of metal oxide nanoparticles, producing them more effective against ROS-generated apoptosis and showing negligible toxicity towards normal cells. CONCLUSION: The utilization of plant phytochemicals in metal oxide nanoparticle production presents a safe, eco-friendly, sustainable, and effective approach to developing effective and safer cancer nanomedicines. Green synthesis not only increases anticancer activity but also decreases the biocompatibility problems associated with the physiochemical synthetic approach. Further research needs to concentrate on improving this synergy to create a targeted phytochemical-based metal oxide nanoparticle for cancer therapeutics.
背景:金属氧化物纳米颗粒具有独特的性质,如生物相容性、卓越的反应活性以及产生活性氧的能力,因此在癌症治疗中引起了极大的关注。各种金属氧化物纳米颗粒,如氧化铈、氧化铜、氧化铁、二氧化钛和氧化锌,已针对多种癌症进行了研究,包括脑癌、乳腺癌、宫颈癌、结肠癌、白血病、肝癌、肺癌、黑色素瘤、卵巢癌和前列腺癌。然而,传统的金属氧化物纳米颗粒物理化学合成方法通常包含有毒物质,这一主要问题引发了对其生物相容性和安全性的质疑。 目的:本研究旨在探讨植物植物成分在通过绿色合成制备金属氧化物纳米颗粒过程中的作用,并探索金属氧化物纳米颗粒在治疗多种癌症方面的治疗效果。主要研究植物植物成分(酚类化合物、黄酮类化合物、糖苷、生物碱等)在金属氧化物纳米颗粒制备中的潜力,以及它们对多种癌症更强的靶向能力。 方法:对近期文献进行了系统检索,重点是利用植物植物成分(植物提取物)制备绿色金属氧化物纳米颗粒。分析了植物植物化学物质(存在于植物的不同部位,如叶子、花朵、茎、果皮和根)及其在绿色金属氧化物纳米颗粒合成中的作用,以及它们对多种癌症的抗癌活性。还重点研究了它们的抗癌机制,该机制涉及活性氧的产生、氧化应激的生成,以及通过凋亡导致癌症抑制。 结果:植物化学物质介导的金属氧化物纳米颗粒合成显示出许多优点,如改善生物相容性和增强对癌细胞的敏感性。植物提取物中存在的植物化学物质充当天然封端剂、还原剂和稳定剂,促进纳米颗粒的合成,从而产生协同抗癌活性。此外,各种植物化学物质的天然抗氧化和抗癌活性增强了金属氧化物纳米颗粒的治疗潜力,使其对活性氧诱导的凋亡更有效,并且对正常细胞的毒性可忽略不计。 结论:在金属氧化物纳米颗粒生产中利用植物植物化学物质为开发有效且更安全的癌症纳米药物提供了一种安全、环保、可持续且有效的方法。绿色合成不仅增加了抗癌活性,还减少了与物理化学合成方法相关的生物相容性问题。进一步的研究需要集中在改善这种协同作用,以创建一种用于癌症治疗的基于植物化学物质的靶向金属氧化物纳米颗粒。
Appl Biochem Biotechnol. 2024-6
Anticancer Agents Med Chem. 2019