Cellulose ethers and their use
View Patent ↗Cellulose ethers are described herein which are useful in capsules or in coatings for dosage forms. In these cellulose ethers the ether substituents are methyl groups, hydroxyalkyl groups, and optionally alkyl groups being different from methyl, the cellulose ether has an MS (hydroxyalkyl) of 0.05 to 1.00, and hydroxy groups of anhydroglucose units are substituted with methyl groups such that [s23/s26−0.2*MS(hydroxyalkyl)] is 0.35 or less, wherein s23 is the molar fraction of anhydroglucose units wherein only the two hydroxy groups in the 2- and 3-positions of the anhydroglucose unit are substituted with methyl groups and wherein s26 is the molar fraction of anhydroglucose units wherein only the two hydroxy groups in the 2- and 6-positions of the anhydroglucose unit are substituted with methyl groups.
1. A cellulose ether wherein
the ether substituents are methyl groups, hydroxyalkyl groups, and optionally alkyl groups being different from methyl,
the cellulose ether has an MS(hydroxyalkyl) of 0.05 to 1.00, and
hydroxy groups of anhydroglucose units are substituted with methyl groups such that [s23/s26−0.2*MS(hydroxyalkyl)] is 0.30 or less,
wherein MS(hydroxyalkyl) is the average number of hydroxyalkyl groups which are bound by an ether bond per mole of anhydroglucose unit,
wherein s23 is the molar fraction of anhydroglucose units wherein only the two hydroxy groups in the 2- and 3-positions of the anhydroglucose unit are substituted with methyl groups and
wherein s26 is the molar fraction of anhydroglucose units wherein only the two hydroxy groups in the 2- and 6-positions of the anhydroglucose unit are substituted with methyl groups and
the cellulose ether has a viscosity of from 2 to 200 mPa·s according to ASTM D2363-79, measured as a 2 wt.-% weight solution in water at 20° C.
2. The cellulose ether of claim 1 being a hydroxyalkyl methyl cellulose.
3. The cellulose ether of claim 2 being a hydroxypropyl methylcellulose and [s23/s26−0.2*MS(hydroxyalkyl)] being 0.27 or less.
4. The cellulose ether of claim 3 having a DS(methyl) of 1.2 to 2.2, wherein DS(methyl) is the average number of OH groups substituted with methyl groups per anhydroglucose unit and wherein a 20 weight percent aqueous solution of the cellulose ether meets the equation
[(gelation temperature[° C.]/1[° C.])−(150*MS(hydroxyalkyl)]<20,
wherein the gelation temperature is the temperature at which G′/G″=1,
G′ being the storage modulus and G″ being the loss modulus of the 20 weight percent aqueous solution of the cellulose ether.
5. The cellulose ether of claim 2 being a hydroxyethyl methylcellulose and [s23/s26−0.2*MS(hydroxyalkyl)] being 0.27 or less.
6. The cellulose ether of claim 1 having a DS(methyl) of 1.2 to 2.2, wherein DS(methyl) is the average number of OH groups substituted with methyl groups per anhydroglucose unit.
7. The cellulose ether of claim 1 wherein a 20 weight percent aqueous solution of the cellulose ether meets the equation
[(gelation temperature[° C.]/1[° C.])−(150*MS(hydroxyalkyl)]<10,
wherein the gelation temperature is the temperature at which G′/G″=1,
G′ being the storage modulus and G″ being the loss modulus of the 20 weight percent aqueous solution of the cellulose ether.
8. A capsule shell comprising the cellulose ether of claim 1 .
9. A capsule comprising the capsule shell of claim 8 .
10. A process for the manufacture of capsules comprising the step of contacting an aqueous composition comprising the cellulose ether of claim 1 with dipping pins.
11. A process for coating a dosage form comprising the step of contacting an aqueous composition comprising the cellulose ether of claim 1 with the dosage form.
12. An aqueous composition for the manufacture of capsules or coatings of dosage forms comprising from 7 to 40 weight percent of a cellulose ether, based on the total weight of the aqueous composition,
wherein in the cellulose ether
the ether substituents are methyl groups, hydroxyalkyl groups, and optionally alkyl groups being different from methyl,
the cellulose ether has an MS(hydroxyalkyl) of 0.05 to 1.00, and
hydroxy groups of anhydroglucose units are substituted with methyl groups such that [s23/s26−0.2*MS(hydroxyalkyl)] is 0.30 or less,
wherein MS(hydroxyalkyl) is the average number of hydroxyalkyl groups which are bound by an ether bond per mole of anhydroglucose unit,
wherein s23 is the molar fraction of anhydroglucose units wherein only the two hydroxy groups in the 2- and 3-positions of the anhydroglucose unit are substituted with methyl groups and
wherein s26 is the molar fraction of anhydroglucose units wherein only the two hydroxy groups in the 2- and 6-positions of the anhydroglucose unit are substituted with methyl groups and
the cellulose ether has a viscosity of from 2 to 200 mPa·s according to ASTM D2363-79, measured as a 2 wt.-% weight solution in water at 20° C.
13. A dosage form being coated with a composition comprising a cellulose ether
wherein in the cellulose ether
the ether substituents are methyl groups, hydroxyalkyl groups, and optionally alkyl groups being different from methyl,
the cellulose ether has an MS(hydroxyalkyl) of 0.05 to 1.00, and
hydroxy groups of anhydroglucose units are substituted with methyl groups such that [s23/s26−0.2*MS(hydroxyalkyl)] is 0.30 or less,
wherein MS(hydroxyalkyl) is the average number of hydroxyalkyl groups which are bound by an ether bond per mole of anhydroglucose unit,
wherein s23 is the molar fraction of anhydroglucose units wherein only the two hydroxy groups in the 2- and 3-positions of the anhydroglucose unit are substituted with methyl groups and
wherein s26 is the molar fraction of anhydroglucose units wherein only the two hydroxy groups in the 2- and 6-positions of the anhydroglucose unit are substituted with methyl groups and
the cellulose ether has a viscosity of from 2 to 200 mPa·s according to ASTM D2363-79, measured as a 2 wt.-% weight solution in water at 20° C.