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Effect of high-nitrogen fertilizer on gliadin and glutenin subproteomes during kernel development in wheat(Triticum aestivum L.) 被引量:2
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作者 Shoumin Zhen Xiong Deng +4 位作者 Xuexin Xu Nannan Liu Dong Zhu Zhimin Wang Yueming Yan 《The Crop Journal》 SCIE CAS CSCD 2020年第1期38-52,共15页
Nitrogen(N),a macronutrient essential for plant growth and development,is needed for biosynthesis of protein and starch,which affect grain yield and quality.Application of high-N fertilizer increases plant growth,grai... Nitrogen(N),a macronutrient essential for plant growth and development,is needed for biosynthesis of protein and starch,which affect grain yield and quality.Application of high-N fertilizer increases plant growth,grain yield,and flour quality.In this study,we performed the first comparative analysis of gliadin and glutenin subproteomes during kernel development in the elite Chinese wheat cultivar Zhongmai 175 under high-N conditions by reversed-phase ultra-performance liquid chromatography and twodimensional difference gel electrophoresis(2D-DIGE).Application of high-N fertilizer led to significant increases in gluten macropolymer content,total gliadin and glutenin content,and the accumulation of individual storage protein components.Of 126 differentially accumulated proteins(DAPs)induced by high-N conditions,24 gliadins,12 high-molecularweight glutenins,and 27 low-molecular-weight glutenins were significantly upregulated.DAPs during five kernel developmental stages displayed multiple patterns of accumulation.In particular,gliadins and glutenins showed respectively five and six accumulation patterns.The accumulation of storage proteins under high-N conditions may lead to improved dough properties and bread quality. 展开更多
关键词 Bread wheat High nitrogen GLIADINS GLUTENINS rp-uplc 2D-DIGE
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反相超高效液相色谱法测定水质中的乙酸含量 被引量:3
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作者 谭松林 《绿色科技》 2017年第20期40-41,共2页
研究了反相超高效液相色谱法测定水质中乙酸含量的色谱条件。结果表明:在Waters T3(50mm×3mm×1.8μm)色谱柱上,以NaH2PO4(20mM/L,pH=2.6)/H3PO4缓冲液作为流动相,210nm处紫外检测水质中的乙酸;其流动相流速为0.2mL/min,柱温30... 研究了反相超高效液相色谱法测定水质中乙酸含量的色谱条件。结果表明:在Waters T3(50mm×3mm×1.8μm)色谱柱上,以NaH2PO4(20mM/L,pH=2.6)/H3PO4缓冲液作为流动相,210nm处紫外检测水质中的乙酸;其流动相流速为0.2mL/min,柱温30℃,进样量1.0μL。该方法简便快捷,样品加标回收率为68.5%~72.1%。 展开更多
关键词 反相超高效液相 紫外检测
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A Stability Indicating UPLC Method for Finasteride and Its Related Impurities
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作者 Y. Koti Reddy G. V. Subba Reddy +1 位作者 K. N. Jaya Veera Kishore Kumar Hotha 《American Journal of Analytical Chemistry》 2012年第11期737-745,共9页
The objective of the present research work is to develop a gradient, reversed-phase liquid chromatographic (RP-UPLC) method for the determination of Finasteride in pharmaceutical bulk drugs for assay and its related i... The objective of the present research work is to develop a gradient, reversed-phase liquid chromatographic (RP-UPLC) method for the determination of Finasteride in pharmaceutical bulk drugs for assay and its related impurities. The chromatographic separation was achieved on a Waters ACQUITY UPLC BEH Phenyl Column (150 mm × 2.1 mm, 1.7 μm), The gradient LC method employs solutions A and B as mobile phase. The solution A Contains 2.5 mM ortho phosphoric acid (Buffer) and solution B contains a mixture of acetonitrile and water in the ratio of (90:10 v/v). The flow rate was 0.22 ml/min and the detection wavelength was 210 nm. In the developed UPLC method, the resolution between Finasteride and its potential impurities, namely Imp-1, Imp-2, Imp-3 and Imp-4 was found to be greater than 2.0. The drug was subjected to stress conditions of hydrolysis, oxidation, photolysis and thermal degradation. Considerable degradation was found to occur in alkaline medium and oxidative stress conditions. Degradation product formed during oxidative hydrolysis was found to be Imp-1. The stress samples were assayed against a qualified reference standard and the mass balance was found close to 99.5%. The developed RP-UPLC method was validated with respect to linearity, accuracy, precision and robustness. The limit of quantification of Imp-1, Imp-2, Imp-3 and Imp-4 were 0.06, 0.06, 0.05 and 0.036% (of analyte concentration, i.e. 0.5 mg/ml) with 1μl injection volume. The developed method was found to be linear in the range of 2.5 - 15 μg/mL with correlation coefficient of 0.999 for assay procedures and found to be linear in the range of 0.05 - 3 μg/mL with correlation coefficient of 0.999 for related impurities. 展开更多
关键词 rp-uplc FORCED DEGRADATION Validation FINASTERIDE METHOD Development
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基于RP-UPLC-MS和HILIC-UPLC-MS的骨疏丹对糖皮质激素性骨质疏松模型大鼠干预作用的尿液代谢组学研究 被引量:16
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作者 黄月 武晓 +4 位作者 薄云海 汪秋伊 秦峰 赵龙山 熊志立 《中国药学杂志》 CAS CSCD 北大核心 2016年第23期2045-2052,共8页
目的建立反相超高效液相色谱-质谱(RP-UPLC-MS)及亲水相互作用超高效色谱-质谱(HILIC-UPLC-MS)代谢组学方法,研究骨疏丹干预糖皮质性骨质疏松模型大鼠尿液代谢物的变化,探索与该病症密切相关的代谢模式及骨疏丹抗骨质疏松作用的代谢途... 目的建立反相超高效液相色谱-质谱(RP-UPLC-MS)及亲水相互作用超高效色谱-质谱(HILIC-UPLC-MS)代谢组学方法,研究骨疏丹干预糖皮质性骨质疏松模型大鼠尿液代谢物的变化,探索与该病症密切相关的代谢模式及骨疏丹抗骨质疏松作用的代谢途径。方法基于代谢组学研究策略,建立正常大鼠、糖皮质性骨质疏松模型大鼠和给予骨疏丹干预大鼠尿液的RP-UPLC-MS与HILIC-UPLC-MS代谢指纹谱,采用主成分分析法(PCA)研究给药前后内源性代谢物变化,寻找潜在生物标志物,探讨骨疏丹的作用机制。结果在RP-UPLC-MS模式下发现了如苯乙酰甘氨酸、N2-琥珀酰-L-鸟氨酸等极性较小的代谢物,而在HILIC-UPLC-MS模式下发现了如甜菜碱、次黄嘌呤等极性较大的代谢物,2种检测模式下共发现了22个潜在生物标志物,这些标志物主要和氨基酸代谢、脂代谢、能量代谢、肠道菌群代谢及肾损伤和体内的氧化应激状态相关。而骨疏丹可以调节骨质疏松模型大鼠体内上述代谢通路并使其向正常状态恢复。结论该研究结果表明,整合RP-UPLC-MS和HILIC-UPLC-MS 2种检测手段可以较全面的表征大鼠体内内源性代谢物轮廓,同时也表明代谢组学在中药整体药效评价、作用机制的研究等方面具有很好的应用前景。 展开更多
关键词 反相超高效液相色谱-质谱 亲水相互作用超高效色谱-质谱 代谢组学 骨疏丹 尿液
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RP-UPLC-PDA法同时测定不同产地雷公藤饮片中6个活性成分
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作者 周国梁 宿树兰 +3 位作者 尚尔鑫 钱大玮 段金廒 俞浩 《药物分析杂志》 CAS CSCD 北大核心 2024年第7期1137-1144,共8页
目的:建立同时测定雷公藤饮片中雷公藤甲素、雷公藤内酯酮、雷酚内酯、雷公藤次碱、雷公藤内酯甲、雷公藤红素6个活性成分RP-UPLC-PDA分析方法。方法:雷公藤饮片采用乙酸乙酯超声提取,甲醇溶解分离,利用RP-UPLC-PDA法对其6个成分进行定... 目的:建立同时测定雷公藤饮片中雷公藤甲素、雷公藤内酯酮、雷酚内酯、雷公藤次碱、雷公藤内酯甲、雷公藤红素6个活性成分RP-UPLC-PDA分析方法。方法:雷公藤饮片采用乙酸乙酯超声提取,甲醇溶解分离,利用RP-UPLC-PDA法对其6个成分进行定量分析,采用Acquity^(TM)UPLC BEH C_(18)(100 mm×2.1 mm,1.7μm)色谱柱,柱温30℃,以乙腈(A)-0.1%甲酸水(B)为流动相,进行梯度洗脱,流速0.4 mL·min^(-1),进样量2μL。结果:6个活性成分在测定浓度范围内线性关系良好(0.9992≤r≤0.9997);加样回收试验中平均回收率为99.2%~103.1%,RSD为1.2%~2.9%。对10批不同产地雷公藤饮片进行含量测定,结果显示不同产地饮片中成分含量具有差异性,雷公藤甲素含量最高为140.2μg·g^(-1),最低为103.2μg·g^(-1);雷公藤内酯酮含量最高为224.7μg·g^(-1),最低为112.2μg·g^(-1);雷酚内酯含量最高为306.7μg·g^(-1),最低为189.6μg·g^(-1);雷公藤次碱含量最高为283.2μg·g^(-1),最低为211.2μg·g^(-1);雷公藤内酯甲含量最高为31.2μg·g^(-1),最低为16.8μg·g^(-1);雷公藤红素含量最高为87.6μg·g^(-1),最低为52.1μg·g^(-1)。结论:建立RP-UPLC-PDA法能够同时测定雷公藤饮片中6个成分,方法稳定,结果可靠,适用于雷公藤饮片定量分析测定。 展开更多
关键词 雷公藤饮片 反相超高效液相色谱-二极管阵列检测法 不同产地 雷公藤甲素 雷公藤内酯酮 雷酚内酯 雷公藤次碱 雷公藤内酯甲 雷公藤红素 定量分析
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基于RP-UPLC-MS技术的人血清样品脂质组学分析 被引量:1
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作者 殷婷婷 赵铁 赵春杰 《沈阳药科大学学报》 CAS CSCD 北大核心 2016年第8期627-631,共5页
目的建立基于RP-UPLC-MS技术的人血清样本脂质组学分析方法。方法以人血清为样本,利用甲醇-氯仿(体积比为2∶1,含质量分数为0.01%的BHT)混合溶剂进行脂质提取,优化液相色谱条件及质谱检测参数并对人血清中甘油三酯、甘油磷脂酰胆碱、溶... 目的建立基于RP-UPLC-MS技术的人血清样本脂质组学分析方法。方法以人血清为样本,利用甲醇-氯仿(体积比为2∶1,含质量分数为0.01%的BHT)混合溶剂进行脂质提取,优化液相色谱条件及质谱检测参数并对人血清中甘油三酯、甘油磷脂酰胆碱、溶血性甘油磷脂酰胆碱等代表性脂质类成分进行方法学考察。结果建立了以Acquity BEH C_(18)(5 cm×1.0 mm,1.7μm)为分析柱,柱温50℃,以乙腈-异丙醇(体积比为5∶2,含质量分数为1%的甲酸铵)为流动相A,超纯水(含质量分数为1%的甲酸铵)为流动相B,梯度方式洗脱,采用正负离子检测模式电喷雾电离(±ESI)方式进行质谱检测的RP-UPLC-MS人血清样本脂质组学分析方法,且方法学考察结果表明该方法精密度、稳定性及重复性均良好。结论该方法适用于人血清样本的脂质组学研究,为临床疾病脂类生物标志物的寻找奠定了基础。 展开更多
关键词 脂质组学 反相超高效液相色谱-质谱联用 血清
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