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作 者:张源[1] 关春杰[1] 冀蔚佳 耿子颖[1] 白小红[1] 杨官娥[1]
出 处:《中医药导报》2016年第17期43-46,共4页Guiding Journal of Traditional Chinese Medicine and Pharmacy
基 金:太原市科技项目人才专项明星专题(120247-08);国家自然科学基金项目(81173473);山西省自然科学基金项目(2010011048-2);2012年山西省高等学校大学生创新创业训练项目(201231)
摘 要:目的:建立HPLC法同时测定丹参沼泽红假单胞菌转化液中丹参素、原儿茶醛、迷迭香酸、丹酚酸B和丹酚酸A5种成分的含量,并和丹参对照液进行比较。方法:采用HPLC法,色谱柱为岛津InertSustainC18柱(4.6mm×250mm,5μm);甲醇-0.1%磷酸水梯度洗脱;检测波长为287nm,流速为0.8mL·min^-1,柱温为26℃,进样量为25μL。结果:丹参素、原儿茶醛、迷迭香酸、丹酚酸B和丹酚酸A分别在20-1000μg·mL^-1,5-200μg·m^-1,5~200μg·mL^-1,5~1000μg·mL^-1,10~200μg·mL^-1范围内呈良好的线性关系(r〉0.9997)。加样回收率分别为101.31%,101.13%,98.81%,103.47%,99.06%。结论:该方法准确可靠,具有良好的精密度、重复性、稳定性和回收率,可以用于丹参沼泽红假单胞菌转化液中5个酚酸类成分含量的同时测定,为丹参沼泽红假单胞菌转化液的进一步研究奠定基础。Objective: To establish a HPLC method for determination tanshinol, protocatechualdehyde, ros- marinic acid, salvianolic acid B and salvianolic acid A in Salvia miltiorrhizha Bunge extraction bioconverted by Rhodopseudomonas palustris, and to compare with salvia miltiorrhiza control liquid. Methods: HPLC was applied on a SHIMADZU InertSustain C18 column (4.6mm×250 mm, 5 μm) with methanol-0.1% phosphoric acid water as mobile phase by gradient elution. The detection wavelength was 297 nm, and the flow rate was 0.8 mL·min ^-1; the column temperature was 26 ℃ and the injection volum was 25μL. Results: Tanshinol, protocatechualdehyde, rosmarinic acid, salvianolic acid B and salvianolic acid A presented a good linearity (r〉0.9997) in the concen- tration ranges of 20~1000 μg·mL^-1, 5-200 μg·mL^-1, 5-200 μg·mL^-1, 5~1000 μg·mL^-1 and 10-200 μg·mL^-1 re- spectively. The recovery was 101.31%, 101.13%, 98.81%, 103.47% and 99.06% respectively. Conclusions: The methoed is accurate and reliable, with good precision, repeatability, stability and recovery. It can be used to de- termine the five phenolic acids in Salvia miltiorrhizha Bunge extraction bioconverted by Rhodopseudomonas palustris simultaneously. The study provides scientific basis for further research of S. miltiolvhizha Bunge bio- transformed by Rhodopseudomonas palustris.
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