Pharmaceutical composition comprising temozolomide ester

1. A pharmaceutical composition having activity of anti-tumor comprising a therapeutically effective amount of one or more compounds of formula I as the active ingredient, conventional pharmaceutically acceptable carriers, and one or more pharmaceutically acceptable acidic components, wherein said acidic component is selected from a group consisting of oleic acid, stearic acid, linolenic acid, fumaric acid, benzoic acid, tartaric acid, sorbic acid, lactic acid, citric acid, acetic acid and EDTA,

wherein X is O or S;

R is substituted or unsubstituted C3˜C10 straight or branched alkyl, C3˜C10 cycloalkyl, C3˜C10 straight or branched alkenyl or C3˜C10 straight or branched chain alkynyl;

and R has substituent(s), said substituent(s) is C1˜C6 alkyl, C1˜C6 alkoxy, C1C6 alkylthio group, C1˜C6 alkyl amino group, phenyl or phenyl substituted by halogen.

2. The pharmaceutical composition of claim 1 , wherein said composition further comprises one or more pharmaceutically acceptable C3˜C8 tertiary alcohol or secondary alcohol, or their ester or ether derivatives.

3. The pharmaceutical composition of claim 1 , wherein said active ingredient is administered to patients in a dosage of 0.1˜200 mg/kg body weight/day.

4. The pharmaceutical composition according to claim 3 , wherein said dosage 15 range of the active ingredient is 1˜20 mg/kg body weight/day.

5. The pharmaceutical composition according to claim 1 , wherein said composition is made into any one of pharmaceutically acceptable preparation forms.

6. The pharmaceutical composition according to claim 5 , wherein said composition is made into topically administered transdermal preparation form or orally administered preparation form.

7. The pharmaceutical composition according to claim 6 , wherein said topically administered transdermal preparation form is topically transdermal patch.

8. The pharmaceutical composition according to claim 7 , wherein said topically transdermal patch is the matrix type controlled-release patch, the solid reservoir type controlled-release patch or liquid reservoir type controlled-release patch.

9. The pharmaceutical composition according to claim 8 , wherein said topically transdermal patch is solid reservoir type controlled-release patch, in which the water phase is water and the oil phase is one or more substances selected from a group consisting of following: oleic acid, isopropyl myristate, lauric acid, beeswax, cetyl alcohol, stearyl alcohol, liquid paraffin, vaseline, anhydrous lanolin, stearic acid, cottonseed oil, castor oil and linolenic acid.

10. The pharmaceutical composition according to claim 9 , wherein said oil phase is oleic acid or isopropyl myristate.

11. The pharmaceutical composition according to claim 8 , wherein said topically transdermal patch is liquid reservoir type controlled-release patch containing of non-permeable matrix liquid drug, rate-moderate membrane, PSAs and release layer, wherein: the non-permeable matrix is one or more substances selected from a group consisting of the following: polyethylene, PVC, nitroglycerin, polydimethylsiloxane, PVP, polyvinyl alcohol, complex of polyethene oxide, polyethylene glycol, polyethylene glycol monomethyl ether or polyethylene glycol dimethyl ether, polyethylene glycol succinate and vitamin E TPGS, wool and cotton;

said rate-moderate membrane is selected from a group consisting of membrane of copolymer of the ethylene and vinyl acetate, membrane of polyurethane or membrane of glycol diacetate; and

said PSAs is selected from a group consisting of polysiloxane pressure-sensitive gum or polyacrylate pressure-sensitive gum.

12. The pharmaceutical composition according to claim 11 , wherein said matrix is polyethylene or PVC.

13. The pharmaceutical composition according to claim 8 , wherein said topically administered transdermal patch is the matrix type controlled-release patch, the auxiliary of drug adhesive matrix in the patch is selected from a group consisting of PVC, polyacrylate, polydimethylsiloxane, PVP, polyvinyl alcohol, water gel madeof gel, PVP, complex of PVP and polyethylene oxide, polyethylene glycol monomethyl ether or polyethylene glycol dimethyl ether, polyethylene glycol succinate and VE TPGS.

14. The pharmaceutical composition according to claim 13 , wherein the auxiliary of drug adhesive matrix is polyacrylate.

15. The pharmaceutical composition according to claim 5 , wherein said preparation form is tablet, pill, dispersed powder, capsule, granule, emulsion, solution, suspension, syrup, solid suppository for vaginal or rectal administration.

16. A method to prepare the composition of claim 9 , comprising of the following steps:

weighing an appropriate amount of compound of formula I as the active ingredient and pulverizing into fine powder, into which add water phase, oil phase, surfactant and needed carriers to mix well;

continuing to add the pulverized drug powder to blend to make into microemulsion;

adding an appropriate amount of rate-mederated membrane and pressure-sensitive adhesive to stir well;

degassing by heat preservation using water bath and spreading on a polyethylene matrix; and

drying and cutting to little pieces to give said solid reservoir type controlled-release patch.