Substituted and bridged pyridines useful as calcium channel blockers |
| OF THE INVENTION The specific substituted and bridged pyridine compounds of this invention are ... |
|
Ace inhibitors in macular degeneration |
| OF THE INVENTION The novel method of treatment of senile macular degeneration of this invention ... |
|
Derivatives of 2,3,4,5,6,7-hexahydro-2,7-methano-1,5-benzoxazonines and -1,4-benzoxazonines, processes for their production and their use as pharmaceuticals |
| We claim: 1. 2,3,4,5,6,7-Hexahydro-2,7-methano-1,5-benzoxazonine and -1,4-benzoxazonine compounds, ... |
|
Novel benzylalcohol derivatives and processes for preparing the same |
| What we claim is: 1. A compound of the formula: ##STR11## wherein R is a lower alkyl group having 1-... |
|
Method of use of bicycloheptane substituted prostaglandin analogs as cardiovascular agents |
| What is claimed is: 1. A method of inhibiting arachidonic acid-induced platelet aggregation and ... |
|
Dihydropyridine derivatives and pharmaceutical composition thereof |
| OF THE INVENTION This invention relates to dihydropyridine derivatives represented by the formula (... |
|
Use of fedotozine in the treatment of functional states of intestinal obstructions |
| We claim: 1. Process for inhibiting functional ileus in a patient, which consists of administering ... |
|
Manufacture of pharmaceutical dosage forms |
| OF THE INVENTION The present invention is directed to solid, unit dosage forms primarily for oral ... |
|
|
Therapeutic compositions with enhanced bioavailability
| Details |
Inventors: Martin, Frederick H.; Tsuk, Andrew G.;
Assignee: American Home Products Corporation (New York, NY)
Primary Examiner: Phillips; Delbert R.
Assistant Examiner:
Attorney, Agent or Firm: Mandel; Adley F.
Novel compositions comprising wetted mixtures of poorly soluble drugs with water soluble polymers useful in increasing bioavailability are disclosed. |
|
DETAILED DESCRIPTION OF THE INVENTION This invention relates to compositions of a drug with a water soluble polymer which has been treated with a wetting sufficient amount of a wetting agent selected from anionic and cationic surfactants. In preferred embodiments the composition is a solid, usually a powder, which is then compounded into suitable solid dosage forms for oral administration. Griseofulvin is a known antibiotic which has been found useful in the treatment of certain fungus diseases of plants, man and animals. Griseofulvin as discussed in the background of this invention is also known as a poorly soluble or water soluble drug, which in vivo provides a low order of bioavailability when administered orally. Thus the composition of the instant invention is particularly useful for griseofulvin and drugs of a similar nature such as certain steroids and antibiotics which due to their low aqueous solubility and/or high melting point are poorly absorbed. Illustrative of such drugs are medrogestone; progesterone; estradiol; 10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-carboxamide; 5H-dibenzo[a,d]cycloheptene-5-carboxamide and the like. The compositions of this invention, as will soon be appreciated, further permit the formulation of solid dosage forms which may contain high concentrations of the particular drug, such as griseofulvin, with no concomitant loss of bioavailability usually associated with such high concentrations. These compositions thus allow the preparation of elegant solid dosage forms. The compositions of this invention are also resistant to agglomeration of the drug particles or the tendency of the drug in storage to produce undesirable crystal formation which adversely affects bioavailability of the drug. Polymers useful in this invention include water soluble polymers which are nontoxic and pharmacologically acceptable, particularly for oral administration. Illustrative of polymers, found suitable in this invention include polyvinylpyrrolidone, hydroxypropyl methyl cellulose, hydroxypropyl cellulose, methyl cellulose, block co-polymers of ethylene oxide and propylene oxide, and polyethylene glycol
|
| Related patents |
|
|
Medicament adsorbates and their preparation
In particular, it has been found that a good tasting medicament adsorbate is produced from admixing about 1 to about 25% by weight of a medicament drug with about 8 to ...
|
|
|
Sustained release formulations
We claim: 1. In combination, a drug suitable for oral delivery and a delivery system for sustained release dosage of said drug comprising: (a) a core portion containing ...
|
|
|
Water dispersible gemfibrozil compositions
What is claimed is: 1. A water-dispersible formulation of gemfibrozil comprising finely divided particles of pure gemfibrozil uniformly coated with a mixture of a wax ...
|
|
|
Method and composition for enhancing the effect of indirect-acting sympathomimetic amines
OF SPECIFIC EMBODIMENTS In accordance with this invention, tyrosine or a tyrosine precursor such as phenylalanine is administered concomitnatly with an indirect-acting ...
|
|
|
1-azabicycloalkane derivatives, their preparation process and their use as medicaments
What is claimed is: 1. A compound of formula (I) ##STR5## in which n represents the number 1, R.sub.1 and R.sub.2, identical or different represent hydrogen or an ...
|
|
|
Use of specific N-methyl-D-aspartate receptor antagonists in the prevention and treatment of neurodegeneration
OF THE INVENTION The novel method of treatment of neurodegeneration of this invention comprises the administration to a patient in need of such treatment with an ...
|
|
|
Iron citrate complex, process for its production, and its pharmaceutical
We claim: 1. An iron citrate micellar complex, which is a brown solid having the properties set out below: (a) average composition by weight of about: 10.6% carbon, 2.62%...
|
|
|
Novel 4,5-Bis (4-methoxyphenyl)-2-(pyrrol-2-yl) thiazoles and pharmaceutical composition containing the same
OF INVENTION The 4,5-bis(4-methoxyphenyl)-2-(pyrrol-2-yl)thiazoles of the present invention have the formula (I) as described hereinbefore. In the formula (I), the ...
|
|
|
Specifically .beta.-.beta. cross-linked hemoglobins and method of preparation
The present invention provides a modified hemoglobin comprising hemoglobin which is cross-linked with a cross-linking reagent, said cross-linking reagent being selected ...
|
|
|
Apparatus for manufacturing granulated material
The invention proceeds from the consideration that it is not possible to reduce the width of the slit, especially at high production rates i.e., at high relative ...
|
|
|