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Biomedical subjects

S Marton

Publications and source records attributed to S Marton.

36 records · Page 2Linked to original sources
PubMed1987

Biopharmaceutical investigation of fenoprofen.

The salts of fenoprofen formed with different metals have shown various crystal forms and solubility. The calcium salt has proved the most suitable characteristics for tablet and capsule production. Dissolution and absorption parameters of this substance were studied using in vitro and in vivo methods. The absorption rate and the correlation between pH and membrane diffusion rate constant were investigated in vitro using the "Sartorius" apparatus. The dissolution rate--depending on pH--was investigated by the oscillometric method. The in vivo disintegration of an experimental sample was compared with a commercial preparation. The comparison has been documented by endoscopic photography.

Biopharmaceutics↗
PubMed1984

A new method for high-performance liquid chromatographic determination of drotaverine in plasma.

A sensitive, specific high-performance liquid chromatographic procedure was developed for the determination of plasma drotaverine levels. Basic plasma samples were adjusted to pH 1.5 and extracted with chloroform. HPLC [n-heptane-dichloromethane-diethylamine (50:25:2)] on a microporous silica column, with a variable-wavelength UV detector set at 302 nm allowed the measurement of drotaverine at the 50-ng/mL level. The utility of this method for determination of drotaverine in dog and rat plasma was demonstrated.

Animals↗
PubMed1983

Biopharmaceutical aspects of Depogen.

The absorption of Depogen was studied on an in vitro model and in various laboratory animals using stoichiometrically equivalent doses of drotaverin (No-Spa) calculated for drotaverin base for comparison. Blood levels of the drug were assessed by radiochemical and microchemical methods. Based on the results obtained and pharmacokinetic properties, the expectable optimal dosage and formulations for the possible field of indication were elaborated.

Animals↗
PubMed1979

The absorption and excretion rates of a new pyrido[1,2-a] pyrimidine derivative (Chinoin 123) in rats.

The metabolism and absorption of a potential new drug, Chinoin 123, having an antiatherogenic effect, were studied in rats. Using different methods it was confirmed that the main metabolite of the drug is a free acid form, formed by ester hydrolysis. In Sartorius Resorption Model only the gastric absorption was confirmed and calculated. In vivo experiments in rats showed rather good absorption. The blood and urine concentrations of the drug were determined.

Administration, Oral↗
PubMed1976

The fate of Depogen in rats.

Studying the metabolism of Depogen in rats we have worked out a method for the purification, isolation and separation of the drug and its potential metabolites. In the basic fraction we have found the same metabolic pathway of Drotaverin published earlier by us. In the focus of our recent work was the fate of the theophylline-7-acetic acid and its eventual biotransformed products. We have stated that theophylline-7-acetic acid contrasts with the theophylline excresa in unchanged form, which has been confirmed by several methods.

Acetates↗
PubMedDate not supplied

Correlation between disintegration, dissolution and in vivo absorption rate in the case of compounds with benzyl-isoquinoline structures and its pharmacokinetic aspects.

Investigations have proved that in the case of po preparations disintegration time, dissolution rate and in vivo absorption rate are closely interrelated. These correlations described by adequate mathematical formulas are valid in the case of papaverine, drotaverine and Depogen--compounds with benzyl-isoquinoline structure.

Absorption↗