Abstract: Paris' method for the determination of anthraquinone content of plant drug has been studied. Through the analysis of several drugs, including Rheum palmatum L., Cassia tora L., and Polygonum multiflorum Thunb., more favorable analytical conditions were established; the free and combined anthtaqiiinone contents of a plant drug could thus be determined as follows: Free anthraquinones: 0.1—l.0g finely powdered sample is accurately weighed and extracted with chloroform in a Soxhlet apparatus. The chloroform extract is shaken with successive portions of 5% sodium hydroxide-2% ammonia mixture in a separatory funnel until the alkali solution is colourless. The alkali extracts are combined and diluted to a certain volume. If the solution becomes turbid, it is filtered through a sintered glass filter and the filtrate collected for colorimetric determination in a photometer with a 490 mμ filter. The result is calculated from a calibration curve obtained with 1,8-dihydroxyanthraquinone. The extraction with the mixed alkali solution and the colorimetric measurements must be done in a shaded room to prevent the decomposition of the coloured solution by light. Combined anthraquinones: 0.05—0.1g finely powdered sample is accurately weighed and placed in a 100 ml conical flask, 30 ml of 5 N sulphuric acid are added, and the mixture is refluxed for two hours to hydrolyse the combined anthraquinones. The flask is cooled, then refluxed with 30 ml chloroform for one hour. The latter is removed with a dropper, replaced by a fresh portion of 20 ml chloroform and refluxed for 20 minutes. This extraction process is repeated until anthraquinones are exhausted. The chloroform extracts are combined, washed with small portions of distilled water, extracted with the mixed alkali solution as above, and determined colorimetrically. This gives the total anthraquinone content, from which is subtracted the amount of free anthraquinones in order to get the percentage of combined anthraquinones.