Method for purification of paclitaxel from paclitaxel-containing materials
This invention relates to methods for purification of paclitaxel from a paclitaxel-containing material. The method comprises the following steps: (a) extracting a paclitaxel-containing material with an organic solvent to obtain an extract, and concentrating the extract; (b) adding the concentrate with an organic solvent which is not mixed with water to separate an organic solvent phase and then concentrating; (c) subjecting the concentrate to normal phase chromatography to obtain an eluate; (d) dissolving the eluate in an acetone or dichloromethane followed by adding pentane or hexane to form a precipitate; and (e) subjecting the precipitate to high performance liquid chromatography. According to the method of the present invention, paclitaxel of over 99.5% purity can be easily obtained from a Taxus genus plant with a high yield.
1. A method of purifying paclitaxel, consisting essentially of:
(a) extracting a plant belonging to a Taxus genus, a cell, or a cell culture thereof, with an organic solvent to obtain an extract, and concentrating the extract;
(b) adding an organic solvent which is not mixed with water to the concentrate to separate an organic solvent phase and then concentrating;
(c) subjecting the concentrate to normal phase chromatography to obtain an eluate;
(d) dissolving the eluate in an acetone or dichloromethane followed by adding pentane or hexane to form a precipitate, wherein about 5 to 100 mg of the eluate is dissolved in 1 ml of acetone or dichloromethane, and pentane or hexane is added in an amount such that the precipitate upon subjecting to high performance liquid chromatography yields paclitaxel of at least 99.5% purity;
(e) subjecting the precipitate to high performance liquid chromatography; and
(f) recovering paclitaxel of at least said purity, wherein the volume ratio of acetone or dichloromethane to pentane or hexane is in a range of 1:3 to 1:20.
2. The method of claim 1 , wherein the organic solvent of the step (a) is at least one selected from the group consisting of methanol, ethanol, propanol, and dichloromethane.
3. The method of claim 1 , wherein the organic solvent of the step (b) is selected from the group consisting of an alkylhalide, ether, alcohols of C 4 –C 6 , ethyl acetate, and methyl ethyl ketone.
4. The method of claim 3 , wherein the organic solvent of the step (b) is selected from the group consisting of dichloromethane, carbon tetrachloride, chloroform, 1,2-dichloroethane, di-ethyl ether, methyl-t-butyl ether, di-iso-propyl ether, n-butanol, and n-pentanol.
5. The method of claim 1 , wherein the concentrate of the step (c) is dissolved in at least one solvent selected from the group consisting of dichloromethane, methanol, benzene, acetone, hexane, and ethyl acetate.
6. The method of claim 1 , wherein the elution of the step (c) is subjected with a mixture of methanol and dichloromethane of 0.5˜10%:99.5˜90% (v/v).
7. The method of claim 1 , wherein equilibrium solvent of the step (c) comprises 0.1˜5% (v/v) of methanol and 99.9˜95% (v/v) of dichloromethane, and the elution solvent comprises 0.5˜100% (v/v) of methanol and the rest of dichloromethane.
8. A method of purifying paclitaxel, consisting essentially of the steps of:
(a) extracting a plant belonging to a Taxus genus, a cell, or a cell culture thereof, with an organic solvent to obtain an extract, and concentrating the extract;
(b) adding an organic solvent which is not mixed with water to the concentrate to separate an organic solvent phase and then concentrating;
(c) subjecting the concentrate to normal phase chromatography to obtain an eluate;
(d) dissolving the eluate in methanol followed by adding water to form a precipitate, wherein about 5 to 100 mg of the eluate is dissolved in 1 ml of methanol, and water is added in an amount such that the precipitate upon subjecting to high performance liquid chromatography yields paclitaxel of at least 99.5% purity;
(e) subjecting the precipitate to high performance liquid chromatography; and
(f) recovering paclitaxel of at least said purity, wherein the volume ratio of methanol to water is in a range of 1:3 to 1:20.
9. The method of claim 8 , wherein the organic solvent of the step (a) is at least one selected from the group consisting of methanol, ethanol, propanol, and dichloromethane.
10. The method of claim 8 , wherein the organic solvent of the step (b) is selected from the group consisting of an alkylhalide, ether, alcohols of C 4 –C 6 , ethyl acetate, and methyl ethyl ketone.
11. The method of claim 10 , wherein the organic solvent of the step (b) is selected from the group consisting of dichloromethane, carbon tetrachloride, chloroform, 1,2-dichloroethane, di-ethyl ether, methyl-t-butyl ether, di-iso-propyl ether, n-butanol, and n-pentanol.
12. The method of claim 8 , wherein the concentrate of the step (c) is dissolved in at least one solvent selected from the group consisting of dichloromethane, methanol, benzene, acetone, hexane, and ethyl acetate.
13. The method of claim 8 , wherein the elution of the step (c) is subjected with a mixture of methanol and dichloromethane of 0.5˜10%:99.5˜90% (v/v).
14. The method of claim 8 , wherein equilibrium solvent of the step (c) comprises 0.1˜5% (v/v) of methanol and 99.9˜95% (v/v) of dichloromethane, and the elution solvent comprises 0.5˜100% (v/v) of methanol and the rest of dichloromethane.