Nanoformulations of Plant-Derived Compounds as Emerging Therapeutic Approach for Colorectal Cancer.

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY Current drug delivery Pub Date : 2023-01-01 DOI:10.2174/1567201819666220823155526
Hossein Biganeh, Sahand Mirzaei Dizaji, Yasamin Davatgaran Taghipour, Ghulam Murtaza, Roja Rahimi
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引用次数: 2

Abstract

Background: Colorectal cancer (CRC) represents one of the most daunting health problems accompanied by progressive undesirable socio-economic effects. Phytochemicals, bioactive ingredients majorly found in plants, have gained momentum for their potential against CRC occurrence and regression. However, these phytoconstituents are not exempt from biopharmaceutical drawbacks; therefore, novel strategies, especially nanotechnology, are exploited to surmount the aforementioned bottlenecks. The current paper aims to comprehensively review the phytochemical-based nanoformulations and their mechanisms in the setting of CRC.

Methods: Electronic databases including Scopus, PubMed, and Web of Science were searched with the keywords "colon cancer" or "colorectal cancer", and "plant", "phytochemical", "extract", or "herb", and "nano", "nanoformulation", "Nanoencapsulation", "nanoparticle", "nanostructure", or "nanoliposome", until January 2021.

Results: Of the 1230 research hits, only 69 articles were consequently analyzed. The results indicated nanoformulations of several secondary plant metabolites such as berberine, camptothecin, colchicine, apigenin, chrysin, fisetin, quercetin, curcumin, gallic acid, resveratrol, and ursolic acid have profound effects in a broad range of preclinical models of CRC. A wide variety of nanoformulations have been utilized to deliver these phytochemicals, such as nanocomposite, nanocolloids, and mesoporous silica nanoparticles, which have consequently decreased tumor angiogenesis and mitochondrial membrane potential, increased radical scavenging activity, induced cell cycle arrest at different phases of the cancer cell cycle, and induction of apoptosis process via decreased anti-apoptotic proteins (BRAF, CD44, and Bcl-2) and increased in pro-apoptotic ones (Bax, Fas, caspase 3,8, and 9), as well as modulated biopharmaceutical properties. Chitosan and PEG and their derivatives are among the polymers exploited in the phytochemicals' nanoformulations.

Conclusion and perspective: To conclude, nanoformulated forms of natural ingredients depicted outstanding anti-CRC activity that could hold promise for help in treating CRC. However, well-designed clinical trials are needed to build up a whole picture of the health profits of nanoformulation of natural products in CRC management.

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植物源化合物纳米制剂作为治疗结直肠癌的新途径。
背景:结直肠癌(CRC)是最令人生畏的健康问题之一,并伴有不良的社会经济影响。植物化学物质(Phytochemicals)是一种主要存在于植物中的生物活性成分,因其在防治结直肠癌发生和消退方面的潜力而受到广泛关注。然而,这些植物成分也不能免于生物制药的缺点;因此,新的策略,特别是纳米技术,被用来克服上述瓶颈。本文旨在全面综述植物化学纳米制剂及其在结直肠癌中的作用机制。方法:以关键词“结肠癌”或“结直肠癌”、“植物”、“植物化学”、“提取物”或“草药”、“纳米”、“纳米配方”、“纳米胶囊”、“纳米颗粒”、“纳米结构”或“纳米脂质体”等检索Scopus、PubMed、Web of Science等电子数据库,检索截止日期为2021年1月。结果:在1230篇研究点击中,只有69篇文章被分析。结果表明,几种次生植物代谢物的纳米制剂,如小檗碱、喜树碱、秋水仙碱、芹菜素、大黄素、非塞酮、槲皮素、姜黄素、没食子酸、白藜芦醇和熊果酸,在广泛的CRC临床前模型中具有深远的影响。各种各样的纳米制剂已被用于传递这些植物化学物质,如纳米复合材料、纳米胶体和介孔二氧化硅纳米颗粒,它们因此降低了肿瘤血管生成和线粒体膜电位,增加了自由基清除活性,在癌细胞周期的不同阶段诱导细胞周期阻滞,并通过降低抗凋亡蛋白(BRAF、CD44、和Bcl-2),促凋亡因子(Bax、Fas、caspase 3、8和9)的表达增加,以及生物制药特性的调节。壳聚糖和聚乙二醇及其衍生物是植物化学物质纳米配方中开发的聚合物。结论与展望:综上所述,纳米形式的天然成分具有出色的抗结直肠癌活性,有望帮助治疗结直肠癌。然而,需要精心设计的临床试验来全面了解天然产品纳米配方在结直肠癌管理中的健康效益。
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来源期刊
Current drug delivery
Current drug delivery PHARMACOLOGY & PHARMACY-
CiteScore
5.10
自引率
4.20%
发文量
170
期刊介绍: Current Drug Delivery aims to publish peer-reviewed articles, research articles, short and in-depth reviews, and drug clinical trials studies in the rapidly developing field of drug delivery. Modern drug research aims to build delivery properties of a drug at the design phase, however in many cases this idea cannot be met and the development of delivery systems becomes as important as the development of the drugs themselves. The journal aims to cover the latest outstanding developments in drug and vaccine delivery employing physical, physico-chemical and chemical methods. The drugs include a wide range of bioactive compounds from simple pharmaceuticals to peptides, proteins, nucleotides, nucleosides and sugars. The journal will also report progress in the fields of transport routes and mechanisms including efflux proteins and multi-drug resistance. The journal is essential for all pharmaceutical scientists involved in drug design, development and delivery.
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