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作 者:李超[1] 王远红[1] 杨爽[1,2] 吕志华 LI Chao;WANG Yuan-hong;YANG Shuang;LV Zhi-hua(Key Laboratory of Marine Drugs,Ministry of Education,Shandong Key Laboratory of Glycoscience and Glycotechnology,School of Medicine and Pharmacy,Ocean University of China,Qingdao 266003,China;Laboratory for Marine Drugs and Bioproducts of Qingdao Pilot National Laboratory for Marine Science and Technology,Qingdao 266237,China)
机构地区:[1]中国海洋大学海洋药物教育部重点实验室山东省糖科学与糖工程重点实验室医药学院,山东青岛266003 [2]青岛海洋科学与技术试点国家实验室海洋药物与生物制品功能实验室,山东青岛266237
出 处:《中国海洋药物》2022年第5期65-72,共8页Chinese Journal of Marine Drugs
基 金:山东省“蓝色药库”技术创新工程专项项目(2018SDKJ0401);中央高校基本科研业务费专项(201964019)资助。
摘 要:目的 制定山东省地方习用药材海参的质量标准。方法 参照《中国药典》(2020版)相关方法对海参药材进行性状和薄层色谱(TLC)鉴别研究,测定了水分、酸不溶性灰分及浸出物的含量;通过硫酸苯酚法以葡萄糖为对照品测定海参多糖的含量;采用高效液相色谱法(HPLC)对海参药材的特征图谱进行研究。结果 不同批次海参药材的性状特征较一致;TLC斑点清晰,重复性好;海参药材中水分的质量分数为6.1%~10.8%,酸不溶性灰分的质量分数为0.08%~1.44%,浸出物的质量分数范围为33.6%~51.7%,以葡萄糖计海参多糖的质量分数范围为0.52%~0.85%;供试品色谱图中呈现的5个特征峰与对照药材参照物色谱图中的5个特征峰的保留时间相对应。结论 建立的定性及定量方法操作简便、准确、稳定,可用于海参药材的质量控制。Objective To establish the quality standards of the local medicinal sea cucumber in Shandong Province. Methods According to the relevant methods of the Chinese Pharmacopoeia(2020 edition), the properties and thin-layer chromatography(TLC) identification of sea cucumber medicinal materials were studied. The contents of water, acid-insoluble ash and extracts were determined. The content of sea cucumber polysaccharides was determined by ultraviolet-visible spectrophotometry. The characteristic chromatogram of sea cucumber medicinal materials was studied using the HPLC method. Results The traits of different batches of sea cucumber medicinal materials were relatively consistent. TLC spots were clear and reproducible. The water content in sea cucumber medicinal materials was 6.1%–10.8%, the acid-insoluble ash content was 0.08%–1.44%, and the extract content was 33.6%–51.7%. Calculated by glucose, sea cucumber polysaccharide content was 0.52%–0.85%. The retention time of the five characteristic peaks in the chromatogram of the test samples corresponds to that of the reference medicinal material. Conclusion The method established was simple, accurate and stable, and could be used for the quality control of sea cucumber medicinal materials.
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