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Delayed release formulations containing 3 - (3-dimethylamine-1-ethyl-2-methyl-propyl) phenol or a pharmaceutically acceptable phenolic salt and oral tablets
专利权人:
GRÜNENTHAL GMBH
发明人:
IRIS ZIEGLER,JOHANNES BARTHOLOMAUS
申请号:
ARP160101684
公开号:
AR104921A2
申请日:
2016.06.07
申请国别(地区):
AR
年份:
2017
代理人:
摘要:
A delayed release pharmaceutical preparation containing 3 - (3-dimethylamine-1-ethyl-2-methyl-propyl) phenol or a pharmaceutically acceptable phenyl salt, contained in the delayed release matrix of the active substance, Tables 1 to 80 contain one or more hydrofluoroalkane or hydrofluoroalkane polymers by weight as an acceptable matrix for the drug and show the next release rate measured by the paddle p method in a test tubeh. Eur. At 75 revolutions / min. in a buffer according to Ph. Eur. at pH 6.8 at 37 ° C with UV spectrometry detection. 3-35% by weight (based on 100% by weight of active substance) of 3- (3-dimethylamino-1-ethyl-2-methyl-propyl) phenol released after 0.5 hours5-50% by weight of 3- (3-dimethylamino-2-ethyl-2-methyl-propyl) phenol released after 1 hour, 10-75% by weight of 3- (3-dimethylamino-1-ethyl-2 -methyl-propyl) phenol released after 2 hours, 15-82% by weight of 3- (3-dimethylamino-1-ethyl-2-methyl-propyl) phenol released after 3 hours, 30-97% by weight of 3- (3-Dimethylamino-1-ethyl-2-methyl-propyl) phenol released after 6 hours, more than 50% by weight of 3- (3-dimethylamino-1-ethyl-2-methyl-propyl-phenol released after 12 hours, more than 70% by weight of 3- (3-dimethylamino-1-ethyl-2-methyl-propyl) phenol released after 18 hours, more than 80% by weight of 3- (3-dimethylamino- 1-ethyl-2-methyl-propyl) phenol released after 24 hours.Formulación farmacéutica con liberación retardada que contiene 3-(3-dimetilamino-1-etil-2-metil-propil)fenol o una sal farmacéuticamente aceptable del mismo, en una matriz con liberación retardada de sustancia activa, conteniendo la matriz 1 a 80% en peso de uno o varios polímeros hidrófilos o hidrófobos como formadores de matriz farmacéuticamente aceptables y que presenta in vitro la siguiente velocidad de liberación medida con aplicación del método Paddle Ph. Eur. a 75 revoluciones/min. en un tampón según Ph. Eur. a pH 6,8 a 37ºC con detección espectrométria UV. 3-35% en peso (referido a 100% en peso de sust
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