[Objectives] This study was conducted to establish the quality control standards for Pandanus tectorius Soland.[Methods] Microscopic identification and thin layer chromatography were used to identify and determine the...[Objectives] This study was conducted to establish the quality control standards for Pandanus tectorius Soland.[Methods] Microscopic identification and thin layer chromatography were used to identify and determine the moisture,total ash and extract contents.[Results] The root transection is near round.The outmost side is velamen.There are nearly 10 columns of collenchyma tissue cells inside.In the cortex,there are a large number of fiber bundles scattered,and there are also large mucous cells scattered.The endodermis is distinct,and the cells are small and closely arranged.The pericycle is distinct and forms a ring.The pericycle fiber bundles are arranged in a radial shape by more than 40 bundles of phloem and xylem alternately.The leaf transection is V-shaped.The collenchyma lies under the epidermis.The spongy tissue has many calcium oxalate square crystal and needle crystals.The mucous cells contain calcium oxalate square crystal and needle crystals.The thin layer identification indicated that in the chromatogram of each test sample,spots of the same colors appeared at the positions corresponding to the chromatogram of the reference medicinal material,and the reproducibility was good.The moisture contents of the 10 batches of samples were all below 8.0%.The total ash was below 8.0%.The acid-insoluble ash was below 2.0%.With 50% ethanol as the solvent,the extract contents were all over 12.5%.[Conclusions] The microscopic identification results are reliable and can be used as the identification basis of P.tectorius.The thin layer identification method and the test results can provide a basis for quality control of P.tectorius.展开更多
基金Supported by Study on Quality Evaluation and Standards of Guangxi Zhuang Medicine(MZY2013017)Guangxi Key Laboratory of Zhuang Yao Medicine(GKJZ[2014]32)Zhuang Yao Medicine Collaborative Innovation Center(GJKY[2013]20)
文摘[Objectives] This study was conducted to establish the quality control standards for Pandanus tectorius Soland.[Methods] Microscopic identification and thin layer chromatography were used to identify and determine the moisture,total ash and extract contents.[Results] The root transection is near round.The outmost side is velamen.There are nearly 10 columns of collenchyma tissue cells inside.In the cortex,there are a large number of fiber bundles scattered,and there are also large mucous cells scattered.The endodermis is distinct,and the cells are small and closely arranged.The pericycle is distinct and forms a ring.The pericycle fiber bundles are arranged in a radial shape by more than 40 bundles of phloem and xylem alternately.The leaf transection is V-shaped.The collenchyma lies under the epidermis.The spongy tissue has many calcium oxalate square crystal and needle crystals.The mucous cells contain calcium oxalate square crystal and needle crystals.The thin layer identification indicated that in the chromatogram of each test sample,spots of the same colors appeared at the positions corresponding to the chromatogram of the reference medicinal material,and the reproducibility was good.The moisture contents of the 10 batches of samples were all below 8.0%.The total ash was below 8.0%.The acid-insoluble ash was below 2.0%.With 50% ethanol as the solvent,the extract contents were all over 12.5%.[Conclusions] The microscopic identification results are reliable and can be used as the identification basis of P.tectorius.The thin layer identification method and the test results can provide a basis for quality control of P.tectorius.
文摘以蝾螺内脏为材料,通过硫酸铵沉淀分级分离、SephadexG 200分子筛柱层析和两次DEAE SephadexA 50离子交换柱层析纯化,获得聚丙烯酰胺凝胶电泳单一纯的N 乙酰 β D 氨基葡萄糖苷酶酶制剂.纯酶的比活力为1448U·mg-1.酶的紫外特征吸收峰在275nm处,内源荧光发射峰在340nm处.以对 硝基苯 N 乙酰 β D 氨基葡萄糖为底物,研究酶催化底物水解的反应动力学,结果表明:酶的最适pH为4.5,最适温度为45℃.该酶在pH3.5～6.0区域较稳定,而在pH>7能很快失活;在40℃以下处理30min,酶活力保持稳定,高于40℃,酶稳定性较差,很快失活.酶促反应动力学符合米氏双曲线方程,测得米氏常数Km为3.13mmol·L-1,最大反应速度Vm为17.68μmol·L-1·min-1.
