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NOVEL COMBINATION OF NON-SEDATIVE ANTI-HISTAMINES CONTAINING SUBSTANCES WHICH INFLUENCE THE ACTION OF LEUKOTRIENE, FOR TREATING RHINITIS, OR CONJUNCTIVITIS
专利权人:
MEDA PHARMA GMBH & CO. KG
发明人:
KUSS, HILDEGARD,ENGEL, JUERGEN,SZELENYI, ISTVAN
申请号:
HU0204079
公开号:
HU228927B1
申请日:
2001.02.05
申请国别(地区):
HU
年份:
2013
代理人:
摘要:
Pharmaceutical composition comprises (separately or in combination): (A) a non-sedating antihistamine (or its salt), other than compounds of the loratadine type; (B) a leukotriene antagonist (or its salt) comprising (B1) leukotriene D 4 antagonists, (B2) 5-lipoxygenase inhibitors or (B3) FLAP (5-lipoxygenase activating protein) antagonists; and (C) conventional carriers and/or extenders or auxiliaries. Independent claims are included for the following: (i) the use of a combination of (A)-(C) for the preparation of a medicament for use as above; (ii) a medicament comprising (A)-(C), for use as above; and (iii) the preparation of the medicaments, by mixing and formulating the appropriate components. - ACTIVITY : Antiallergic; antiinflammatory; ophthalmological. In tests for inhibition of ovalbumin-induced nasal mucosal permeability in sensitized rats, the degree of inhibition was 11% using azelastine alone at 0.01 mg/kg i.p., 7% using montelukast alone at 0.1 mg/kg i.p. and 40% using a combination of azelastine at 0.01 mg/kg i.p. and montelukast at 0.1 mg/kg i.p. - MECHANISM OF ACTION : Antihistamine; leukotriene D 4 antagonist; 5-lipoxygenase inhibitor; FLAP (5-lipoxygenase activating protein) antagonist.
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