番荔枝树皮中Taraxerol的提取、分离、鉴定及其对人前列腺癌细胞(lncap和pc-3)的化学预防作用

S. Surapaneni, T. Prakash
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引用次数: 5

摘要

前列腺癌(PC)是美国男性死亡的首要原因,其增长速度在世界其他地区也在增加。本研究的目的是通过石油醚、氯仿和乙醇对番麻树皮进行连续提取,进行初步的光化学分析。Taraxerol的分离、结构鉴定及前列腺癌的体外检查研究。通过薄层色谱(TLC)、高效液相色谱(HPLC)、紫外、气相色谱-质谱(GC-MS)等光谱技术对其结构进行了分析。采用MTT法、中性红细胞毒性、LDH释放量测定、吖啶橙(AO)和溴化乙啶(EB)双染色法测定前列腺细胞株、LNCaP细胞株和PC-3细胞株的抗增殖作用。用间接ELISA法和DNA片段法对蛋白变性、半胱天冬酶水平进行抑制。网状木参树皮的植物化学研究综述报道了其黄酮、皂苷、三萜和单宁的含量。体外实验表明,所选化合物对肿瘤细胞系具有细胞毒性。caspase活性或水平的升高通常被认为是细胞凋亡的指标。作为评估化合物抗炎潜力的筛选方法,测量了防止白蛋白热相关变性的化合物。
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Comprehensive Assignments of Extraction, Isolation and Characterization of Taraxerol from Bark Annona reticulata L. and Chemopreventive Effect on Human Prostate Cancer Cell Lines (lncap and pc-3)
Prostate Cancer (PC) ruins a foremost cause of death of males in the US as well its growth rate is increased in the rest of the world. The current learning aims to perform a preliminary photochemical analysis by the successive extraction of the bark of Annona reticulata L. using petroleum ether, chloroform, and ethanol. The isolation, structure elucidation and identification of Taraxerol and check up in vitro study in prostate carcinoma. The structure was elucidated by spectroscopic techniques included Thin Layer chromatography (TLC) and High Performance Liquid Chromatography (HPLC), UV and Gas Chromatography-Mass Spectrometric (GC-MS). The prostate cell lines, LNCaP and PC-3 cell lines was cultured and antiproliferative effect by MTT Method, Neutral red cytotoxicity, measurement of LDH release, determinations of apoptosis by Acridine Orange (AO) and Ethidium Bromide (EB) double staining. Inhibition of protein denaturation, caspase levels by indirect ELISA and DNA fragmentation was performed. Investigation of the phytochemical summary on the bark of A. reticulata L. reports the occurrence of flavonoids, saponins, triterpenoid and tannins. In-vitro experiments show the selected compound exhibited of cytotoxicity against the cancer cell lines. An increase in caspase activity or caspase levels is generally considered as indicators of cellular apoptosis. The compounds to prevent heat associated denaturation of albumin are measured as a screening method for assessing anti-inflammatory potential of compounds.
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