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theophylline/krompir
Povezava se shrani v odložišče
9 rezultatov
Robustness of Controlled Release Tablets Based on a Cross-linked Pregelatinized Potato Starch Matrix
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
The aim of this study was to evaluate the potential of a cross-linked pregelatinized potato starch (PREGEFLO® PI10) as matrix former for controlled release tablets. Different types of tablets loaded with diprophylline, diltiazem HCl or theophylline were prepared by direct compression of binary
Higher-plant cyclic nucleotide phosphodiesterases. Resolution, partial purification and properties of three phosphodiesterases from potato tuber.
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Prijava / prijava
1. Three phosphodiesterases that are capable of hydrolysing 3':5'-cyclic nucleotides were purified from potato tubers. 2. The phosphodiesterases were fractionated by (NH4)2SO4 precipitation and CM-cellulose chromatography. The phosphodiesterases were resolved from each other and further purified by
Invivo absorption behaviour of theophylline from starch-methyl methacrylate matrix tablets in beagle dogs.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
This study evaluates in vivo the drug absorption profiles from potato starch-methyl methacrylate matrices(*) using theophylline as a model drug. Healthy beagle dogs under fasting conditions were used for in vivo studies and plasma samples were analyzed by a fluorescence polarization immunoassay
Bioadhesive grafted starch copolymers as platforms for peroral drug delivery: a study of theophylline release.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Nonirritant bioadhesive drug release systems based on starch-acrylic acid graft copolymers prepared by radiation of starch and acrylic acid mixtures with (60)Co were developed for buccal application. The release rate of theophylline (TPL), used as a model drug, depended on the ratio of starch to
A new generation starch product as excipient in pharmaceutical tablets. III. Parameters affecting controlled drug release from tablets based on high surface area retrograded pregelatinized potato starch.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
This paper describes the general applicability of a new pregelatinized starch product in directly compressible controlled-release matrix systems. It was prepared by enzymatic degradation of potato starch followed by precipitation (retrogradation), filtration and washing with ethanol. The advantages
Effects of lubricant-mixing time on prolongation of dissolution time and its prediction by measuring near infrared spectra from tablets.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
The relationship between lubricant-mixing time and dissolution time was investigated, and we established a calibration model to predict dissolution time by near infrared (NIR) spectroscopy and the rationale of the prediction. The bulk powder consisted of theophylline, lactose, and potato starch were
Real-time-monitoring of pharmaceutical properties of medical tablets during direct tableting process by hybrid-tableting-process parameter-time profiles.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Preparation of drug-diluent hybrid powders by dry processing.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
New hybrid powders have been produced by the dry processing of six drugs (oxyphenbutazone, prednisolone, theophylline, indomethacin, phenacetin and aspirin), with potato starch used as a core material, by means of an electric mortar and a powder surface reforming system designed to produce hybrid
In vitro release testing of matrices based on starch-methyl methacrylate copolymers: effect of tablet crushing force, dissolution medium pH and stirring rate.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Direct-compressed matrix tablets were obtained from a variety of potato starch-methyl methacrylate copolymers(1) as sustained-release agents, using anhydrous theophylline as a model drug. The aim of this work was to investigate the influence of the copolymer type, the tablet crushing force and
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