Anticancer activity of gold nanobioconjugates synthesized from Elephantopus scaber (linn.) leaf extract.

IF 1.4 4区 医学 Q4 ONCOLOGY
Ashwini S Shinde, Vijay D Mendhulkar
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引用次数: 2

Abstract

Introduction: Medicinal plants are the major natural resources for the treatment of human ailments including cancer therapy. The current cancer treatments such as surgery, radiation, and chemotherapy affect normal cells too. Thus, treatments like synthesized nanoscale particles using plant extracts have proven to be potential anticancer agent.

Aim of the study: We hypothesize that the gold nanoparticles (AuNPs) synthesized using Elephantopus scaber hydro-methanolic extract may have anti-cancer activity along with their synergistic counterparts with adriamycin (ADR) on human breast cancer MCF-7: human breast cancer (A-549), human oral cancer (squamous cell carcinoma [SCC]-40), and COLO-205: human colon cancer cell lines.

Materials and methods: The phytosynthesized AuNPs were characterized for ultraviolet-visible (UV-Vis) spectroscopy, nanoparticle tracking analysis (NTA), X-ray diffraction, scanning electron microscopy, transmission electron microscopy (TEM), and Fourier transform infrared (FTIR) analysis. The anticancer ability of the AuNPs against human MCF-7, A-549, SCC-40, and COLO-205 through sulforhodamine B assay has been studied.

Results: The synthesis of AuNPs was confirmed with the UV-Vis spectrophotometer with a peak at 540 nm. The FTIR analysis showed polyphenolic groups were major found to be the reduction and capping agent for AuNPs. According to the results obtained, AuNPs showed good anti-proliferative activity with GI50 <10 μg/ml on MCF-7 cancer cell line. The synergistic effect of AuNPs + ADR was even better for all the four cell lines than that of the AuNPs alone.

Conclusion: The green synthesis of AuNPs is a simple, eco-friendly, and cost-effective method with dominantly spherical morphology ranging from 20 to 40 nm confirmed by NTA and TEM analysis. The study reveals the potent therapeutic value of the AuNPs.

大象叶提取物合成金纳米生物偶联物的抗癌活性研究。
药用植物是治疗包括癌症在内的人类疾病的主要天然资源。目前的癌症治疗方法,如手术、放疗和化疗,也会影响正常细胞。因此,使用植物提取物合成纳米级颗粒等治疗方法已被证明是潜在的抗癌剂。研究目的:我们假设用象皮水甲醇提取物合成的金纳米颗粒(AuNPs)可能与阿霉素(ADR)协同对人乳腺癌MCF-7:人乳腺癌(A-549)、人口腔癌(鳞状细胞癌[SCC]-40)和COLO-205:人结肠癌细胞系具有抗癌活性。材料与方法:利用紫外-可见光谱(UV-Vis)、纳米颗粒跟踪分析(NTA)、x射线衍射、扫描电镜、透射电镜(TEM)和傅里叶变换红外(FTIR)对植物合成的AuNPs进行了表征。通过磺胺B法研究了AuNPs对人MCF-7、A-549、SCC-40和COLO-205的抗癌能力。结果:用紫外可见分光光度计证实了AuNPs的合成,峰在540nm处。FTIR分析表明,多酚基团是aunp的主要还原和封盖剂。结论:经NTA和TEM分析证实,AuNPs的绿色合成以20 ~ 40 nm的球形形态为主,是一种简单、环保、经济的绿色合成方法。该研究揭示了aunp的有效治疗价值。
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来源期刊
CiteScore
1.80
自引率
15.40%
发文量
299
审稿时长
6 months
期刊介绍: The journal will cover technical and clinical studies related to health, ethical and social issues in field of Medical oncology, radiation oncology, medical imaging, radiation protection, non-ionising radiation, radiobiology. Articles with clinical interest and implications will be given preference.
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