采用反相高效液相色谱法对发酵液中的风味强化肽进行定量分析。
A reverse phase high performance liquid chromatographic method was developed for the quantitative analysis of enhancing flavor peptide in fermentation.
采用反相高效液相色谱法，同时测定对虾中的五种磺胺类药物残留。
Five kinds of sulfa drugs residues in prawn were determined by RP-HPLC simultaneously.
采用反相高效液相色谱法研究了噻嗪酮在水和水稻植株中的残留动态。
The dynamics of buprofezin residue in water and rice plants has been studied by the high performance liquid chromatographic method.
采用反相高效液相色谱法，建立了一种可同时测定根痛平冲剂中芍药甙和葛根素含量的方法。
This paper described a HPLC method where by paeoniflorin and puerarin in Gentongping granule were simultaneously determined.
采用反相高效液相色谱法和电喷雾质谱法对我国野生笃斯越橘中花青素组分进行了分离和分析。
RP-HPLC method and ESI-MS were established to separate and analyze the component of anthocyanidins from blueberries of Vaccinium uliginosum of China.
方法采用反相高效液相色谱法检测5-脂氧合酶产物——白三烯B4和5-羟花生四烯酸量的变化来反映该酶活性的改变。
Methods 5- LO products, leukotriene B4 (LTB4) and 5 hydroxyeicosatetraenoic(5-HETE), we re determined by RP-HPLC to represent 5-LO activity.
方法采用TLC法对处方中大黄、栀子进行定性鉴别，并采用反相高效液相色谱法对涂膜剂中的大黄素、绿原酸进行含量测定。
METHODS Radix et Rhizoma Rhei, Fructus Gardeniae in this prescription were identified by TLC. The content of Emodin and Chlorogenic acid were determined by HPLC.
方法采用反相高效液相色谱法对30例肿瘤患者静脉滴入MTX（1．0-3．0／次）后的脑脊液和血浆中MTX浓度进行连续测定。
Methods: MTX at a high dose ranging from 1.0 to 3.0 g per course was intravenously administered to 30 patients with malignant tumors.
采用反相高效液相色谱法对三唑磷乳油进行定量分析，其变异系数为0.83%，平均回收率为99.2%，相关系数为0.9986。
A method was described for the quantitative analysis of triazophos by HPLC. The result showed that average recovery rate was 99.2 %, variation coefficient 0.83%, relative coefficient 0.9986.
以胆甾醇为指标性成分进行质量控制，采用反相高效液相色谱法对其进行了含量测定，五批蜣螂药材中胆甾醇的平均含量为0.3381%。
Cholesterin as an index component to control the quality was detected by RP-HPLC, the average content of the cholesterin in five kinds Dung Beetle was 0.3381%.
采用高效液相色谱法，使用反相色谱柱和二极管阵列检测器测定吡·哒可湿性粉剂中吡虫啉和哒螨灵的含量。
Using reversed-phase chromatographic column and diode array detector, content of imidacloprid and pyridaben in their water soluble powder was measured with high effective liquid chromatography.
方法采用柱色谱法分离，反相高效液相色谱法与细胞膜色谱法联用，并结合离体药理实验确定太白花中的有效成分。
METHOD S The effective component was determined by cell membrane chromatography and reversed phase high performance liquid chromatography. The pharmacological actions in vitro were testified.
方法采用柱色谱法分离，反相高效液相色谱法与细胞膜色谱法联用，并结合离体药理实验确定太白花中的有效成分。
METHOD S The effective component was determined by cell membrane chromatography and reversed phase high performance liquid chromatography. The pharmacological actions in vitro were testified.
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