Objective To establish the method for quantitative analysis of chlorogenic acid, hyperoside, quercetin, kaempferol and isorhamnetin in the Cuscuta chinensis different pro- cessed products by HPLC. Methods The Kromasil C18 column (250 ram×4.6 mm,5 μm) was used with methanol-0.4% phosphoric acid as mobile phase. Under the condition of gradient elution, the flow rate was 1.0 mL/min, the column temperature was 30℃ and the detection wavelength was 360 nm. Results Baseline separation was obtained separately for the five kinds of active ingredien...