Pharmaceutical multiple unit particulate formulation in the form of coated cores
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A61K-009/16
A61K-047/02
출원번호
US-0509107
(1995-08-01)
우선권정보
DK-0000695 (1994-06-15)
발명자
/ 주소
Norling Tomas,DKX
Jensen Lone Norgaard,DKX
Hansen Jens,DKX
출원인 / 주소
Dumex-Alpharma A/S, DKX
대리인 / 주소
Watov & Kipnes, P.C.
인용정보
피인용 횟수 :
122인용 특허 :
9
초록▼
A pharmaceutical multiple unit particulate formulation in the form of coated cores which includes a pharmaceutically acceptable carrier selected from calcium carbonate, calcium silicate, calcium magnesium silicate, calcium phosphate, kaolin, sodium hydrogen carbonate, sodium sulfate, barium carbonat
A pharmaceutical multiple unit particulate formulation in the form of coated cores which includes a pharmaceutically acceptable carrier selected from calcium carbonate, calcium silicate, calcium magnesium silicate, calcium phosphate, kaolin, sodium hydrogen carbonate, sodium sulfate, barium carbonate, barium sulfate, magnesium sulfate, magnesium carbonate, and activated carbon, and an active substance in a layer on the outer surface of the cores.
대표청구항▼
[ We claim:] [1.] A pharmaceutical multiple unit particulate formulation comprising individual units in the form of coated cores, wherein at least 50% w/w of the cores before coating have a particle size within a range of about 90-225 .mu.m, when tested as described herein, each coated core comprisi
[ We claim:] [1.] A pharmaceutical multiple unit particulate formulation comprising individual units in the form of coated cores, wherein at least 50% w/w of the cores before coating have a particle size within a range of about 90-225 .mu.m, when tested as described herein, each coated core comprisingi) a pharmaceutically acceptable inert carrier which is present in the core in a first concentration of at least about 20% w/w calculated on the total weight of the core, and which is selected from the group consisting of calcium carbonate, calcium silicate, calcium magnesium silicate, calcium phosphate, kaolin, sodium hydrogen carbonate, sodium sulfate, barium carbonate, barium sulfate, magnesium sulfate, magnesium carbonate, and activated carbon, andii) an active drug substance being present in a layer on the outer surface of the cores,the pharmaceutically acceptable inert carrier being such a material which--when formulated into uncoated cores containing the pharmaceutically acceptable inert carrier optionally in combination with a binder and with a second concentration of the inert carrier of at least 80% w/w calculated on the total weight of the uncoated core--has a friability (weight loss in % w/w) of at the most about 20%, when tested as described herein, and the cores have a flow angle--when tested according to method A described herein using a diameter of the disc outlet of 9 mm--of at the most 30.degree..
연구과제 타임라인
LOADING...
LOADING...
LOADING...
LOADING...
LOADING...
이 특허에 인용된 특허 (9)
Abramowitz Robert (Somerset NJ) Joshi Yatinda M. (Piscataway NJ) Jain Nemichand B. (Monmouth Junction NJ), Captopril formulation providing increased duration of activity.
Arnold Raymond E. (San Francisco CA) Becker Nathaniel T. (Burlingame CA) Boston Matthew G. (San Carlos CA) Mansikkamaki Aino (Hanko CA FIX) Simpson Curran M. (Montara CA) Wendt Daniel J. (Belmont CA), Enzyme-containing granules coated with hydrolyzed polyvinyl alcohol or copolymer thereof.
Volkonsky Viktor A. (Moscow RUX) Dvukhsherstnov Sergei D. (Moscow RUX) Chernyakov Sergei V. (Moscow RUX), Magnetically responsive composition for carrying biologically active substances and methods of production.
Tsuru Sumiaki (Tokyo JPX) Tsugita Masashi (Tokorozawa JPX) Takasaki Ken (Tokyo JPX) Yokoo Akihiko (Tokyo JPX) Ichitsuka Takeshi (Tokyo JPX), Slow release drug delivery granules and process for production thereof.
Bologna William J.,FRX ; Levine Howard L. ; Cartier Philippe,FRX ; de Ziegler Dominique,FRX, Bioadhesive progressive hydration tablets and methods of making and using the same.
Schwarzentruber, Patrick; Di Maiuta, Nicola; Schoelkopf, Joachim; Ridgway, Catherine Jean; Gane, Patrick A. C., Coated controlled release active agent carriers.
Bettini, Ruggero; Arduini, Lauro; Bertolini, Francesca; Camellini, Claudia, Compositions of microparticles and granules for oral controlled release of substances for veterinary use.
Jung, Edward K. Y.; Levien, Royce A.; Lord, Robert W.; Malamud, Mark A.; Rinaldo, Jr., John D.; Wood, Jr., Lowell L., Computational and/or control systems and methods related to nutraceutical agent selection and dosing.
Jung, Edward K. Y.; Levien, Royce A.; Lord, Robert W.; Malamud, Mark A.; Rinaldo, Jr., John D.; Tegreene, Clarence T.; Wood, Jr., Lowell L., Computational systems and methods related to nutraceuticals.
Pather, S. Indiran; Robinson, Joseph R.; Eichman, Jonathan D.; Khankari, Rajendra K.; Hontz, John; Gupte, Sangeeta V., Effervescent drug delivery system for oral administration.
Pather, S. Indiran; Robinson, Joseph R.; Eichman, Jonathan D.; Khankari, Rajendra K.; Hontz, John; Gupte, Sangeeta V., Effervescent drug delivery system for oral administration.
Pather, S. Indiran; Robinson, Joseph R.; Eichman, Jonathan D.; Khankari, Rajendra K.; Hontz, John; Gupte, Sangeeta V., Effervescent drug delivery system for oral administration.
S. Indiran Pather ; Joseph R. Robinson ; Jonathan D. Eichman ; Rajendra K. Khankari ; John Hontz ; Sangeeta V. Gupte, Effervescent drug delivery system for oral administration.
Jung, Edward K. Y.; Levien, Royce A.; Lord, Robert W.; Malamud, Mark A.; Rinaldo, Jr., John D.; Wood, Lowell L., Individualized pharmaceutical selection and packaging.
Beyerinck, Ronald A.; Ray, Roderick J.; Dobry, Dan E.; Settell, Dana M., Method for making homogeneous spray-dried solid amorphous drug dispersions using pressure nozzles.
Beyerinck, Ronald A.; Deibele, Heather L. M.; Dobry, Dan E.; Ray, Roderick J.; Settell, Dana M.; Spence, Ken R., Method for making homogeneous spray-dried solid amorphous drug dispersions utilizing modified spray-drying apparatus.
Beyerinck, Ronald A.; Deibele, Heather L. M.; Dobry, Dan E.; Ray, Roderick J.; Settell, Dana M.; Spence, Ken R., Method for making homogeneous spray-dried solid amorphous drug dispersions utilizing modified spray-drying apparatus.
Beyerinck, Ronald A.; Diebele, Heather L. M.; Dobry, Dan E.; Ray, Roderick J.; Settell, Dana M.; Spence, Ken R., Method for making homogeneous spray-dried solid amorphous drug dispersions utilizing modified spray-drying apparatus.
Jung, Edward K. Y.; Levien, Royce A.; Lord, Robert W.; Malamud, Mark A.; Rinaldo, Jr., John D.; Tegreene, Clarence T.; Wood, Jr., Lowell L., Methods and systems related to receiving nutraceutical associated information.
Jung, Edward K. Y.; Levien, Royce A.; Lord, Robert W.; Malamud, Mark A.; Rinaldo, Jr., John D.; Tegreene, Clarence T.; Wood, Jr., Lowell L., Methods and systems related to transmission of nutraceutical associated information.
Pather, S. Indiran; Robinson, Joseph R.; Eichman, Jonathan D.; Khankari, Rajendra K.; Hontz, John, Pharmaceutical compositions for rectal and vaginal administration.
Singh Shiva P.,INX ; Mukarram Siddiqui Mohammed Jaweed,INX ; Kulkami Dilip Ganesh,INX ; Purohit Manish,INX, Synthetic procedure for 5-methoxy-2-[(4-methoxy-3,5-dimethyl-2-pyridinyl)-methylthio]-IH-benzimidazole hydrochloride and its conversion to omeprazole.
Jung, Edward K. Y.; Leuthardt, Eric C.; Levien, Royce A.; Lord, Robert W.; Malamud, Mark A.; Rinaldo, Jr., John D.; Wood, Jr., Lowell L., Systems and methods for transmitting pathogen related information and responding.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.