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建立高效液相色谱同时测定保健食品中11种功效成分的高通量分析方法。样品前处理采用甲醇-水-磷酸溶液提取,对油脂样品则采用甲醇-水-磷酸溶液与正己烷液液萃取除脂。采用Agilent TC-C18色谱柱(250 mm×4.6 mm,5μm),乙腈-2 g/L辛烷磺酸钠溶液(加入1 m L磷酸)作为流动相,流速1.0 m L/min,梯度洗脱,用二极管阵列检测器串联荧光检测器检测,外标法峰面积定量。VB2在0.25~25 mg/L、VB6在0.5~20 mg/L、烟酸、烟酰胺在1~100 mg/L、其余5种功效成分在0.5~50 mg/L质量浓度范围内线性良好,相关系数r为0.999 1~1.000 0。在样品中待测成分含量约0.5、1倍和2倍3个水平的添加回收率为86.4%~110%之间,相对标准偏差为0.21%~11.7%。方法的定量限:烟酸、烟酰胺为20 mg/kg,其余9种功效成分方法的定量限为10 mg/kg。 相似文献
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Wenjuan Zhang Ying Huai Zhiping Miao Chu Chen Mohamed Shahen Siddiq Ur Rahman 《Drug development and industrial pharmacy》2019,45(3):456-464
Rhodiola rosea L. radix (RRL) is one of the most popular medical herb which has been widely used for the treatment of different diseases effectively, including cardiovascular diseases and nerve system diseases. However, due to the multiple compounds in RRL, the underlying molecular mechanisms of RRL are remained unclear. To decipher the action mechanisms of RRL from a systematic perspective, a systems pharmacology approach integrated absorption, distribution, metabolism, and excretion (ADME) system, drug targeting, and network analysis was introduced. First, by the ADME screening system and the target fishing process, 56 potential active compounds and 62 targets were obtained, respectively. In addition, compound-target network demonstrated that most compounds interacted with multiple targets, indicating that RRL may enhance its therapeutic effects probably through hitting on multiple targets in a holistic level. Moreover, target-pathway network and gene ontology analysis showed that multiple targets of RRL were involved in several biological pathways, i.e. Neuroactive ligand-receptor interaction, calcium signaling pathway, adrenergic signaling in cardiomyocytes, and VEGF signaling pathway, which dissecting the therapeutic effects of RRL on various diseases, such as cardiovascular diseases, depression, adaptation diseases, etc. In summary, this work successfully explains the potential active compounds and the multi-scale curative action mechanisms of RRL for treating various diseases; meanwhile, it implies that RRL could be applied as a novel therapeutic agent in arthritic diseases. Most importantly, this work provides an in silico strategy to understand the action mechanisms of herbal medicines from molecular/system levels, which will promote the new drug development of traditional Chinese medicine. 相似文献
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食用乙醇常温浸提法提取红景天苷 总被引:1,自引:0,他引:1
以超临界CO_2萃取后的高山红景天干粉为原料,进行食用乙醇常温浸提法提取红景天苷的工艺研究,采用正交实验设计筛选出最佳的提取工艺参数为:乙醇浓度为40%,溶剂和原料之比为6:1。常温浸提时间为48h,颗粒度为40目。 相似文献
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为了解长白山地区高山红景天药材的质量,对产自长白山地区不同年限的人工栽培和野生高山红景天中的红景天苷含量和农药残留量进行了测定.在检测波长为275nm、色谱柱为PLATISTLTM C18柱(250mm×4.6mm,5μm)、流动相为甲醇-乙酸铵溶液、线性度(r)高于0.999 8、平均回收率为96.62%、相对标准偏差为1.32%的条件下,采用高效液相色谱法测定了红景天苷的含量;在色谱柱为HP-5毛细管气相色谱柱(0.32mm×30m×0.25μm)、进样口温度为250℃、Ni63电子捕获检测器温度为300℃、尾吹15mL/min、柱温以10℃/min升至220℃并保持20min条件下,采用气相色谱法测定了农药残留.结果表明,不同年限人工栽培品的红景天苷含量有差异,且含量均低于野生品,样品中均无六六六、滴滴涕农药残留. 相似文献
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Dai-Long Fang Yan Chen Bei Xu Ke Ren Zhi-Yao He Li-Li He Yi Lei Chun-Mei Fan Xiang-Rong Song 《International journal of molecular sciences》2014,15(3):3373-3388
Salidroside (Sal) is a potent antitumor drug with high water-solubility. The clinic application of Sal in cancer therapy has been significantly restricted by poor oral absorption and low tumor cell uptake. To solve this problem, lipid-shell and polymer-core nanoparticles (Sal-LPNPs) loaded with Sal were developed by a double emulsification method. The processing parameters including the polymer types, organic phase, PVA types and amount were systemically investigated. The obtained optimal Sal-LPNPs, composed of PLGA-PEG-PLGA triblock copolymers and lipids, had high entrapment efficiency (65%), submicron size (150 nm) and negatively charged surface (−23 mV). DSC analysis demonstrated the successful encapsulation of Sal into LPNPs. The core-shell structure of Sal-LPNPs was verified by TEM. Sal released slowly from the LPNPs without apparent burst release. MTT assay revealed that 4T1 and PANC-1 cancer cell lines were sensitive to Sal treatment. Sal-LPNPs had significantly higher antitumor activities than free Sal in 4T1 and PANC-1 cells. The data indicate that LPNPs are a promising Sal vehicle for anti-cancer therapy and worthy of further investigation. 相似文献
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