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阿克什瓦拉药味在MDA-MB-231细胞中的药物特性及探索

Pharmaceutical characterization and exploration of Arkeshwara rasa in MDA-MB-231 cells.

作者信息

Jayakumar Remya, Dash Manoj Kumar, Kumar Pankaj, Sharma Shiwakshi, Gulati Saumya, Pandey Akanksha, Cholke Kaushavi, Fatima Zeeshan, Trigun S K, Joshi Namrata

机构信息

Department of Rasashastra and Bhaishajya Kalpana, Banaras Hindu University, Varanasi, 221005, India.

Department of Rasashastra and Bhaishajya Kalpana, Government Ayurveda College, Raipur, India.

出版信息

J Ayurveda Integr Med. 2024 Jan-Feb;15(1):100823. doi: 10.1016/j.jaim.2023.100823. Epub 2023 Dec 30.

Abstract

BACKGROUND

The diverse specificity mode of cancer treatment targets and chemo resistance demands the necessity of drug entities which can address the devastating dynamicity of the disease.

OBJECTIVES

To check the anti-tumour potential of traditional medicine rich in polyherbal components and metal nanoparticle namely Arkeshwara rasa (AR).

MATERIAL METHODS

The AR was prepared in a modified version with reference from Rasaratna Samuchaya and characterized using sophisticated instrumental analysis including XRD, SEM-EDAX, TEM, TGA-DSC, and LC-MS and tested against the MDA-MB-231 cell line to screen cell viability and the cytotoxicity with MTT, SRB and the AO assay.

RESULTS

XRD pattern shows cubic tetrahedrite structure with Sb, Cu, S peaks and trace elements like Fe, Mg, etc. The particle size of AR ranges between 20 and 30 nm. The TGA points thermal decomposition at 210 °C and the metal sulphide peaks in DSC. LC-MS analysis reveals the components of the formulation more on the flavonoid portion. The IC value of MTT and SRB are 25.28 μg/mL and 31.7 μg/mL respectively. The AO colorimeter substantiated the cell viability and the apoptosis figures of the same cell line. The AR exhibits cytotoxicity and reaffirms the apoptosis fraction with SRB assay.

CONCLUSIONS

The Hesperidine, Neohesperidin, Rutin components in the phytochemical pool can synergize the anti-tumour potential with either influencing cellular pathways or decreasing chemo resistance to conventional treatment. AR need to be further experimented with reverse transcription, flow cytometry, western blotting, etc.

摘要

背景

癌症治疗靶点的多样特异性模式和化疗耐药性要求有能够应对该疾病毁灭性动态变化的药物实体。

目的

检验富含多种草药成分和金属纳米颗粒的传统药物阿凯什瓦拉·拉萨(AR)的抗肿瘤潜力。

材料与方法

参照《拉萨拉特纳·萨穆查亚》制备改良版的AR,并使用包括X射线衍射(XRD)、扫描电子显微镜-能谱仪(SEM-EDAX)、透射电子显微镜(TEM)、热重-差示扫描量热法(TGA-DSC)和液相色谱-质谱联用仪(LC-MS)等精密仪器分析对其进行表征,并针对MDA-MB-231细胞系进行测试,以通过MTT法、磺酰罗丹明B(SRB)法和吖啶橙(AO)法筛选细胞活力和细胞毒性。

结果

XRD图谱显示具有立方硫锑铜矿结构,有锑、铜、硫峰以及铁、镁等微量元素。AR的粒径在20至30纳米之间。TGA表明在210°C发生热分解,DSC中有金属硫化物峰。LC-MS分析显示该制剂的成分更多集中在黄酮类部分。MTT法和SRB法的半数抑制浓度(IC)值分别为25.28微克/毫升和31.7微克/毫升。AO比色计证实了同一细胞系的细胞活力和凋亡情况。AR表现出细胞毒性,SRB法再次确认了凋亡率。

结论

植物化学物质库中的橙皮苷、新橙皮苷、芦丁成分可通过影响细胞途径或降低对传统治疗的化疗耐药性来协同发挥抗肿瘤潜力。AR需要通过逆转录、流式细胞术、蛋白质免疫印迹等方法进一步试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7786/10792653/f7daea150174/ga1.jpg

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