Green chemistry: Modern therapies using nanocarriers for treating rare brain cancer metastasis from colon cancer

IF 2.7 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Doaa S․R․ Khafaga , Ghazala Muteeb , Darin․W․ Aswa , Mohammad Aatif , Mohd Farhan , Salma Allam
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Abstract

Brain metastasis (BM) from colon cancer is associated with a poor prognosis and restricted treatment alternatives, largely due to issues related to blood-brain barrier (BBB) permeability and the negative effects of standard chemotherapy. Nanotechnology improves treatment efficacy by enabling targeted and controlled drug delivery. This review article evaluates the potential of nanotechnology-based therapies for treating colon cancer BM, emphasizing their capacity to cross the BBB, diminish metastatic growth, and enhance overall survival rates. A review of multiple studies evaluated nanoparticles (NPs) as carriers for chemotherapy, focusing on parameters including particle size, surface charge, and drug-loading capacity. The study also reviewed studies that examined BBB penetration, in vitro tumor accumulation, and in vivo tumor growth inhibition. In vitro findings indicated that NPs accumulate more efficiently in BM tissue than in healthy brain tissue and show significant BBB penetration. In vivo, nanotherapy markedly inhibited tumor growth and prolonged survival relative to conventional chemotherapy or control treatments while also exhibiting reduced side effects. Recent studies demonstrated that plant extracts can effectively and safely synthesize nanomaterials, positioning them as a viable and environmentally friendly precursor for nanomaterial production. Nanotechnology-based therapies demonstrate significant potential in the treatment of colon cancer BM by minimizing systemic toxicity, enhancing therapeutic efficacy, and facilitating more targeted drug delivery. Further research is required to confirm these findings and implement them in clinical practice.

Abstract Image

绿色化学:利用纳米载体治疗结肠癌转移性脑癌的现代疗法。
结肠癌脑转移(BM)与预后不良和治疗方案受限相关,主要是由于血脑屏障(BBB)通透性和标准化疗的负面影响。纳米技术通过实现靶向和受控的药物递送来提高治疗效果。这篇综述文章评估了纳米技术治疗结肠癌转移瘤的潜力,强调了它们穿越血脑屏障、减少转移性生长和提高总体生存率的能力。对纳米颗粒(NPs)作为化疗载体的多项研究进行了回顾,重点关注颗粒大小、表面电荷和载药能力等参数。该研究还回顾了血脑屏障渗透、体外肿瘤积累和体内肿瘤生长抑制的研究。体外研究结果表明,NPs在脑梗死组织中比在健康脑组织中更有效地积累,并表现出明显的血脑屏障渗透。在体内,与常规化疗或对照治疗相比,纳米疗法显著抑制肿瘤生长,延长生存期,同时也显示出更少的副作用。最近的研究表明,植物提取物可以有效和安全地合成纳米材料,使其成为一种可行的、环保的纳米材料前体。基于纳米技术的治疗方法通过最小化全身毒性、提高治疗效果和促进更有针对性的药物传递,在结肠癌BM的治疗中显示出巨大的潜力。需要进一步的研究来证实这些发现并将其应用于临床实践。
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来源期刊
SLAS Discovery
SLAS Discovery Chemistry-Analytical Chemistry
CiteScore
7.00
自引率
3.20%
发文量
58
审稿时长
39 days
期刊介绍: Advancing Life Sciences R&D: SLAS Discovery reports how scientists develop and utilize novel technologies and/or approaches to provide and characterize chemical and biological tools to understand and treat human disease. SLAS Discovery is a peer-reviewed journal that publishes scientific reports that enable and improve target validation, evaluate current drug discovery technologies, provide novel research tools, and incorporate research approaches that enhance depth of knowledge and drug discovery success. SLAS Discovery emphasizes scientific and technical advances in target identification/validation (including chemical probes, RNA silencing, gene editing technologies); biomarker discovery; assay development; virtual, medium- or high-throughput screening (biochemical and biological, biophysical, phenotypic, toxicological, ADME); lead generation/optimization; chemical biology; and informatics (data analysis, image analysis, statistics, bio- and chemo-informatics). Review articles on target biology, new paradigms in drug discovery and advances in drug discovery technologies. SLAS Discovery is of particular interest to those involved in analytical chemistry, applied microbiology, automation, biochemistry, bioengineering, biomedical optics, biotechnology, bioinformatics, cell biology, DNA science and technology, genetics, information technology, medicinal chemistry, molecular biology, natural products chemistry, organic chemistry, pharmacology, spectroscopy, and toxicology. SLAS Discovery is a member of the Committee on Publication Ethics (COPE) and was published previously (1996-2016) as the Journal of Biomolecular Screening (JBS).
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