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31.
目的 建立阿里红中齿孔酸及其总三萜酸的含量测定方法。方法 采用紫外-可见分光光度法测定总三萜酸含量;采用HPLC测定齿孔酸含量。色谱柱为RP-C18柱(4.6 mm×250 mm,5 μm);流动相为乙腈-0.4%磷酸(68∶ 32),检测波长210 nm,流速1.0 mL·min-1,柱温30℃。结果 3批阿里红药材中齿孔酸含量分别为2.3%,2.6%,3.1%;总三萜酸含量分别为27.2%,32.1%,35.9%。结论 所建立的分析方法准确、简便,可为定量评价阿里红药材的质量提供依据。 相似文献
32.
Ji-Wu Huang Fang-You Chen Chuang-Jun Li Jing-Zhi Yang Jie Ma Xiao-Guang Chen 《Journal of Asian natural products research》2018,20(4):337-343
Two new saponins, notoginsenosides Ng1 (1) and Ng2 (2), together with seven known compounds (3–9), were isolated from the leaves of Panax notoginseng. Their structures were elucidated by UV, IR, HRESIMS, and NMR experiments. Compounds 6 and 7 showed moderate cytotoxic activities against HCT-116, with IC50 values of 4.98 and 0.64 μmol/L, respectively. 相似文献
33.
Huilong Wen Zhong Wu Huidong Hu Yixiong Wu Gang Yang Jiajun Lu Guang Yang Gang Guo Qirong Dong 《Journal of natural medicines》2018,72(1):57-63
Pachymic acid (PA) is a lanostane type triterpenoid isolated from Poria cocos, which possesses an anti-tumor effect in breast cancer, prostate cancer, lung cancer, and bladder cancer cells. In this study, we investigated the effect of PA on the growth and apoptosis of human immortalized cell line (HOS) and primary osteosarcoma cells by a Cell Counting Kit-8 (CCK-8) and Annexin V and propidium iodide (PI) staining, respectively. Western blot was used to measure the expression of cleaved Caspase 3, PTEN, and AKT, as well as the AKT phosphorylation. The Caspase 3 activity was determined using the Caspase-3 Colorimetric Assay Kit. From the results, PA significantly reduced cell proliferation in a concentration- and time-dependent manner. PA also induced cell apoptosis in a dose-dependent fashion. PA treatment led to increased Caspase 3 activation and PTEN expression, as well as reduced AKT phosphorylation. Moreover, Ac-DEVD-CHO (a Caspase 3/7 inhibitor) pre-treatment or PTEN knockdown partially blocked the effects of PA on cell proliferation and apoptosis. Caspase 3/7 inhibitor had an additive effect with PTEN knockdown. Collectively, our results suggested that induction of apoptosis by PA was mediated in part by PTEN/AKT signaling and Caspase 3/7 activity. This study provides evidence that PA might be useful in the treatment of human osteosarcoma. 相似文献
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Yang Zhang Bowen Deng Yida Cui Xue Chen Jiayi Bi Guogang Zhang 《Journal of natural medicines》2018,72(4):946-953
Two new secoiridoid glucosides, ilexpublignoside (1), pubzenoside (2), and a new lignan, ilexlignan B (3), along with seven known compounds (4–10) were isolated from the roots of Ilex pubescens for the first time. Their chemical structures were elucidated on the basis of extensive spectroscopic methods, including IR, UV, HR-ESI–MS, CD, NMR experiments, as well as comparison with the reported data. 相似文献
36.
Comparative Efficacy and Safety of Phosphate Binders in Hyperphosphatemia Patients With Chronic Kidney Disease 下载免费PDF全文
Xiuqin Yang MD Qingning Bai MD Yanguo Li MD Haijun Liu MD Haiying Guo MD Xiaolei Zhang MD 《JPEN. Journal of parenteral and enteral nutrition》2018,42(4):766-777
Background: In this study, we coordinated a network meta‐analysis to establish the efficacy and safety of different agents used in the treatment of hyperphosphatemia patients with chronic kidney disease. Methods: PubMed, CNKI, and Embase were systematically searched to retrieve relevant studies. Outcomes were presented by mean differences, odds ratios, and corresponding 95% credible intervals for continuous outcomes and binary outcomes, respectively. Each therapy was ranked according to the value of surface under the cumulative ranking curve. Consistencies between direct and indirect comparisons were assessed with a node‐splitting plot. Results: In terms of efficacy end points (including levels of serum phosphate, serum calcium, serum intact parathyroid hormone, and serum calcium × phosphorus product), all 7 kinds of agents outperformed or performed at least equally to placebo, with iron‐based phosphate‐binding agents being potentially the most effective. As for safety end points (including mortality, adverse events, and all‐cause discontinuation), almost all agents were equivalent in term of mortality and all‐cause discontinuation except in the comparison between iron‐based phosphate‐binding agents and placebo. Meanwhile, iron‐based phosphate‐binding agents colestilan and nicotinic acid performed poorly compared with placebo in terms of adverse events. Furthermore, iron‐based phosphate‐binding agents were potentially the safest agents followed sequentially by calcium‐based phosphate‐binding agents and placebo. Conclusion: Iron‐based phosphate‐binding agents were the preferable agents when considering efficacy and safety simultaneously. 相似文献
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38.
Xinxin Liu Jian Yang Shuang Song Hong Song Danni Ai Jianjun Zhu Yurong Jiang Yongtian Wang 《Australasian physical & engineering sciences in medicine / supported by the Australasian College of Physical Scientists in Medicine and the Australasian Association of Physical Sciences in Medicine》2018,41(2):495-505
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Xiuxia Li Lili Wei Wenru Shang Xin Xing Min Yin Juan Ling Kuoray Mao Yiliang Zhu Kehu Yang 《Zeitschrift fur Gesundheitswissenschaften》2018,26(2):127-135