Objective: To establish the method for determination of luteolin in Caulis et Folium Stauntoniae. Method: The chromatographic conditions was as follows: a Dikma Diamonsil C18 (4.6 mm×250 mm,5 μm) column,a mobile phase of acetonitrile-0.1% H3PO4 (26: 74); and a UV detector at 350 nm. Result: Luteolin was linear in the ranger of 0.067 75-2.168 μg (r=0.999 9); the average recovery of 99.25% (RSD 1.65%), the precision with RSD 2.22%, repetition with RSD 1.24% and stability with RSD 2.58% were obtained. Conclusion: The method is accurate,reliable,and can be used for quality control of the production.