Preparation containing benzimidazole derivative
The present invention relates to a novel formulation comprising a benzimidazole derivative. The formulation for oral administration comprising a compound of Formula 1 according to the present invention or a pharmaceutically acceptable salt thereof; and at least one disintegrant selected from the group consisting of croscarmellose sodium, sodium starch glycolate and low-substituted hydroxypropylcellulose, exhibits an excellent storage stability and has an effect on preventing a phenomenon of decline in dissolution rate, thus being usefully used as a formulation for oral administration.
1. A formulation for oral administration comprising a compound of (S)-4((5,7-difluorochroman-4-yl)oxy)-N,N-2-trimethyl-1H-benzo[d]imidazole-6-carboxamide of Formula 1 or a pharmaceutically acceptable salt thereof; and at least one disintegrant selected from the group consisting of croscarmellose sodium, sodium starch glycolate and low-substituted hydroxypropylcellulose,
wherein the formulation is a tablet; and
wherein a dissolution rate of the tablet increases or decreases by less than 6% from an initial value when stored under a stress condition of 60° C. and 80% relative humidity for 7 days:
2. The formulation for oral administration according to claim 1 , wherein a content of the disintegrant is 1 to 20 wt % of the total weight of the formulation.
3. The formulation for oral administration according to claim 1 , wherein the disintegrant is low-substituted hydroxypropylcellulose having a substitution degree of a hydroxypropoxy group that amounts to 5 to 16 mass %.
4. The formulation for oral administration according to claim 1 , wherein the formulation further comprises at least one ingredient selected from the group consisting of a binder, a filler and a lubricant.
5. The formulation for oral administration according to claim 4 , wherein the binder is at least one selected from the group consisting of starch, microcrystalline cellulose, colloidal silicon dioxide, mannitol, lactose, polyethylene glycol, polyvinyl pyrrolidone co-polymer, hydroxypropyl cellulose, gelatin and a mixture thereof.
6. The formulation for oral administration according to claim 4 , wherein the filler is at least one selected from the group consisting of lactose, microcrystalline cellulose, mannitol and colloidal silicon dioxide.
7. The formulation for oral administration according to claim 4 , wherein the lubricant is at least one selected from the group consisting of stearic acid, magnesium stearate, calcium stearate, sodium benzoate, sodium stearyl fumarate, glyceryl monooleate, glyceryl monostearate, glyceryl behenate, glyceryl palmitostearate, zinc stearate and a paraffin group.