Coated fine particles containing drug for intrabuccally fast disintegrating dosage forms
Regarding an object of sufficient suppression of unpleasant taste in the oral cavity and quick dissolution in the gastrointestinal tract, which is generated when a drug having a strong unpleasant taste such as bitterness, astringency and the like is applied to a quickly disintegrating preparations in the oral cavity, this invention has achieved the aforementioned object for the first time by employing a constitution of coating a coat of a water-soluble polymer and a specified ratio of a pH-independent water-insoluble polymer and hydroxypropylcellulose.
1. Drug containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity, wherein microparticles containing the drug solifenacin or a salt thereof and polyethylene glycol which are present in a homogeneously mixed state are coated with a film comprising a water-soluble polymer, said water-soluble polymer selected from the group consisting of hydroxypropylmethylcellulose, hydroxypropylcellulose, methyl cellulose and a mixture thereof, and are further coated with an outer film comprising:
(1) a pH-independent water-insoluble polymer accounting for 60% or more and less than 79% of the film, wherein the pH-independent water-insoluble polymer is ethyl cellulose; and
(2) hydroxypropylcellulose accounting for more than 21% and 40% or less of the film, wherein the rate of dissolution of drug from the drug-containing coated microparticles using a test liquid simulating inside of the oral cavity is from 0% to 25% in 3 minutes.
2. The drug-containing coated microparticles for use in quickly disintegrating preparations in the oral cavity described in claim 1 , wherein the water-soluble polymer is hydroxypropylmethylcellulose.
3. The drug-containing coated microparticles for use in quickly disintegrating preparations in the oral cavity described in any of claim 1 or 2 , wherein rate of dissolution of drug from the drug-containing coated microparticles using a test liquid simulating inside of the oral cavity is from 0% to 3% in 1 minute and from 0% to 25% in 3 minutes, and rate of dissolution of drug from the drug-containing coated microparticles using a test liquid simulating inside the gastrointestinal tract is 80% or more in 30 minutes.
4. A method for producing drug-containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity, wherein microparticles containing the drug solifenacin or a salt thereof and polyethylene glycol which are present in a homogeneously mixed state are coated with a film comprising a water-soluble polymer, said water-soluble polymer selected from the group consisting of hydroxypropylmethylcellulose, hydroxypropylcellulose, methyl cellulose and a mixture thereof, and are further coated with an outer film comprising:
(1) a pH-independent water-insoluble polymer accounting for 60% or more and less than 79% of the film, wherein the pH-independent water-insoluble polymer is ethyl cellulose; and
(2) hydroxypropylcellulose accounting for more than 21% and 40% or less of the film, wherein the rate of dissolution of drug from the drug-containing coated microparticles using a test liquid simulating inside of the oral cavity is from 0% to 25% in 3 minutes.
5. A quickly disintegrating preparation in the oral cavity containing drug-containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity, wherein microparticles containing the drug solifenacin or a salt thereof and polyethylene glycol which are present in a homogeneously mixed state are coated with a film comprising a water-soluble polymer, said water-soluble polymer selected from the group consisting of hydroxypropylmethylcellulose, hydroxypropylcellulose, methyl cellulose and a mixture thereof, and are further coated with an outer film comprising:
(1) a pH-independent water-insoluble polymer accounting for 60% or more and less than 79% of the film, wherein the pH-independent water-insoluble polymer is ethyl cellulose; and
(2) hydroxypropylcellulose accounting for more than 21% and 40% or less of the film, wherein the rate of dissolution of drug from the drug-containing coated microparticles using a test liquid simulating inside of the oral cavity is from 0% to 25% in 3 minutes.
6. Drug-containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity, wherein microparticles containing solifenacin succinate and polyethylene glycol which are present in a homogeneously mixed state are coated with a film comprising a water-soluble polymer, said water-soluble polymer selected from the group consisting of hydroxypropylmethylcellulose, hydroxypropylcellulose, methyl cellulose and a mixture thereof, and are further coated with an outer film comprising:
(1) a pH-independent water-insoluble polymer accounting for 60% or more and less than 79% of the film, wherein the pH-independent water-insoluble polymer is ethyl cellulose; and
(2) hydroxypropylcellulose accounting for more than 21% and 40% or less of the film, wherein the rate of dissolution of drug from the drug-containing coated microparticles using a test liquid simulating inside of the oral cavity is from 0% to 25% in 3 minutes.
7. The drug-containing coated microparticles for use in quickly disintegrating preparations in the oral cavity described in claim 6 , wherein the water-soluble polymer is hydroxypropylmethylcellulose.
8. The drug-containing coated microparticles for use in quickly disintegrating preparations in the oral cavity described in claim 6 or 7 , wherein rate of dissolution of drug from the drug-containing coated microparticles using a test liquid simulating inside of the oral cavity is from 0% to 3% in 1 minute and from 0% to 25% in 3 minutes, and rate of dissolution of drug from the drug-containing coated microparticles using a test liquid simulating inside the gastrointestinal tract is 80% or more in 30 minutes.
9. A method for producing drug-containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity, wherein microparticles containing solifenacin succinate and polyethylene glycol which are present in a homogeneously mixed state are coated with a film comprising a water-soluble polymer, said water-soluble polymer selected from the group consisting of hydroxypropylmethylcellulose, hydroxypropylcellulose, methyl cellulose and a mixture thereof, and are further coated with an outer film comprising:
(1) a pH-independent water-insoluble polymer accounting for 60% or more and less than 79% of the film, wherein the pH-independent water-insoluble polymer is ethyl cellulose; and
(2) hydroxypropylcellulose accounting for more than 21% and 40% or less of the film, wherein the rate of dissolution of drug from the drug-containing coated microparticles using a test liquid simulating inside of the oral cavity is from 0% to 25% in 3 minutes.
10. A quickly disintegrating preparation in the oral cavity containing drug-containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity, wherein microparticles containing a drug and polyethylene glycol, said drug is solifenacin succinate, which are present in a homogeneously mixed state are coated with a film comprising a water-soluble polymer, said water-soluble polymer selected from the group consisting of hydroxypropylmethylcellulose, hydroxypropylcellulose, methyl cellulose and a mixture thereof, and are further coated with an outer film comprising:
(1) a pH-independent water-insoluble polymer accounting for 60% or more and less than 79% of the film, wherein the pH-independent water-insoluble polymer is ethyl cellulose; and
(2) hydroxypropylcellulose accounting for more than 21% and 40% or less of the film, wherein the rate of dissolution of drug from the drug-containing coated microparticles using a test liquid simulating inside of the oral cavity is from 0% to 25% in 3 minutes.
11. The drug-containing coated microparticles for use in quickly disintegrating preparations in the oral cavity of claim 1 or 6 , wherein the water-soluble polymer is hydroxypropylcellulose.
12. The drug-containing coated microparticles for use in quickly disintegrating preparations in the oral cavity of claim 1 or 6 , wherein the water-soluble polymer is methyl cellulose.
13. A method for producing drug-containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity of claim 4 or 9 , wherein the water-soluble polymer is hydroxypropylmethylcellulose.
14. A method for producing drug-containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity of claim 4 or 9 , wherein the water-soluble polymer is hydroxypropylcellulose.
15. A method for producing drug-containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity of claim 4 or 9 , wherein the water-soluble polymer is methyl cellulose.
16. A quickly disintegrating preparation in the oral cavity containing drug-containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity of claim 5 or 10 , wherein the water-soluble polymer is hydroxypropylmethylcellulose.
17. A quickly disintegrating preparation in the oral cavity containing drug-containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity of claim 5 or 10 , wherein the water-soluble polymer is hydroxypropylcellulose.
18. A quickly disintegrating preparation in the oral cavity containing drug-containing coated microparticles having an average particle diameter of 350 μm or less, for quickly disintegrating preparations in the oral cavity of claim 5 or 10 , wherein the water-soluble polymer is methyl cellulose.