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101.
鲍思伟 《江西师范大学学报(自然科学版)》2005,29(1):77-80
豌豆不同生长期用不同浓度的硫酸锰溶液进行叶面喷施,结果表明,在幼苗期、现蕾期和开花期喷施不同浓度硫酸锰溶液,能增强豌豆叶片的SOD活性和CAT活性,降低O2^*-生成速率和MDA含量.在豌豆生长的幼苗期、现蕾期和开花期叶面喷施0.1%~0.2%的硫酸锰溶液能促进豌豆的生长和产量的增加。 相似文献
102.
受土壤和环境因素的影响,新疆果树患缺铁性黄化病日益增多,通过将硫酸亚铁施入土壤、叶面喷施和树干注射,以及改良土壤、果树育种等途径可予矫治. 相似文献
103.
不同竹龄毛竹材表面颜色、润湿性及化学成分分析 总被引:1,自引:0,他引:1
对不同竹龄毛竹竹材的表面颜色、润湿性及化学成分的变化进行分析。结果表明:随竹龄增加,氙灯照射后毛竹素材表面颜色逐渐变暗加深,颜色变化越来越明显。1年生竹材润湿性最好,2年生竹材润湿性较好,4个月竹材润湿性较弱,4年生竹材润湿性最弱。随竹龄增加,竹材表面半纤维素相对含量增加,木质素相对含量的差异较小;综纤维素含量在4个月至2年生之间逐渐降低,2年生时最低,2年生至10年生之间,变化较小。 相似文献
104.
105.
Rapid extraction and analysis method for the simultaneous determination of 21 bioflavonoids in Siegesbeckia pubescens Makino 下载免费PDF全文
Yaqi Yao Xiao Liang Xiaoqi Sun Lina Yin Hai He Xingjie Guo Zhen Jiang 《Journal of separation science》2015,38(7):1130-1136
A novel and rapid microwave extraction and ultra high performance liquid chromatography coupled with a triple quadrupole‐linear ion trap mass spectrometry method was developed and validated for the determination of 21 bioflavonoids in Siegesbeckia pubescens Makino. The optimal conditions for the extraction of flavonoids from Siegesbeckia pubescens Makino involved the use of methanol as the extraction solvent, a microwave temperature of 70°C, an extraction time of 11 min, and a solvent‐to‐solid ratio of 40 mL/g. Chromatographic separation was achieved on a Waters ACQUITY UPLC BEH C18 column(100 × 2.1 mm, 1.7 μm) with a gradient mobile phase (A: 0.3% v/v aqueous formic acid and B: acetonitrile) at a flow rate of 0.25 mL/min. All calibration curves showed good linearity (r > 0.999) within the test ranges. The method developed was validated with acceptable sensitivity, intra‐ and interday precision, reproducibility, and extraction recoveries. The validated method was successfully applied to determine the contents of 21 bioflavonoids in Siegesbeckia pubescens Makino from different sources. 相似文献
106.
Columbianadin, one of the main bioactive constituents of the roots of Angelica pubescens Maxim. f. biserrata Shan et Yuan, has been found to possess obvious pharmacological effects in previous studies. In this study, a valid and sensitive reverse‐phase high‐performance liquid chromatography (RP‐HPLC) method was established and validated for the determination of columbianadin (CBN) and its active metabolite columbianetin (CBT) in rat tissue samples. Sample separation was performed on an RP‐HPLC column using a mobile phase of MeOH–H2O (75:25, v/v) at a flow rate of 1.0 mL/min. The UV absorbance of the samples was measured at the wavelength 325 nm. The calibration curves for CBN were linear over the ranges of 0.5–20 µg/g for brain, testes and muscle, 1.0–10.0 µg/g for stomach and intestine, and 0.2–20.0 µg/g for heart, liver, spleen, lung and kidney. The calibration curves for CBT were linear over the ranges of 0.5–25 µg/g for stomach and intestine, and 0.1–10.0 µg/g for heart, liver, spleen, lung and kidney. The analysis method was successfully applied to a tissue distribution study of CBN and CBT after intravenous administration of CBN to rats. The results of this study indicated that CBN could be detected in all of the selected tissues after i.v. administration. CBN was distributed to rat tissues rapidly and could be metabolized to CBT in most detected tissues. Of the detected tissues, heart had the highest uptake of CBN, which suggested that heart might be one of the main target tissues of CBN. Concentrations of CBT were obviously higher in the digestive system than in other assayed tissues. The information provided by this research is very useful for gaining knowledge of the capacities of CBN and CBT to access different tissues. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献