EUDRAGIT EPO PDF

Interpolymer interactions between the countercharged polymers like Eudragit® EPO (polycation) and hypromellose acetate succinate. PDF | The objective of this investigation was to evaluate the potential of Eudragit EPO nanoparticles (EPO NP) in improving therapeutic efficacy. Download scientific diagram | Molecular structures of (a) MFA, (b) EUDRAGIT® EPO, and (c) EUDRAGIT® L from publication: Stabilization of a.

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Evonik EUDRAGIT® E PO Copolymer

Tablet thickness of the matrix tablets was examined for six tablets of each batch using an electronic digital caliper. Tablets were exposed to ml of pH 6. Handbook of pharmaceutical excipients.

The spectrum of EE Fig. The carboxylic groups ionize in aqueous media at pH 5. Eudragit E, hypromellose acetate succinate, hypromellose phthalate polyelectrolyte complexation.

Polyelectrolyte complexes-recent developments and open problems. Floating and sustained-release characteristics eudragot effervescent tablets prepared with a mixed matrix of Eudragit L and Eudragit E PO.

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The amount of acetaminophen in matrix tablets was kept constant at mg while the amount of other excipients was varied. Tablets with mg of the polymers were compacted manually from the physical mixtures using a 9-mm punch in a tablet compression machine. In case of Fickian release diffusionaly controlled releasethe n has the limiting values of 0. A physico-chemical approach of polyanion-polycation interactions aimed at better understanding the in vivo behaviour of polyelectrolyte-based drug delivery and gene transfection.

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Indian J Pharm Sci. Ho C, Hwang GC. EE and enteric polymer, at 1: The ratio of dimethylaminoethyl methacrylate groups to butyl methacrylate and methyl methacrylate groups is about 2: For comparative purposes, FT-IR analysis was also performed on pure EE, pure enteric polymers, and an unexposed physical mixture of the polymers.

Subscribe to Premium Services Searches: On analyzing regression coefficient values, it was found that F8 formulation exhibits first-order kinetics 0. The ratio of free carboxyl groups to the ester groups is approximately 1: Acknowledgments The authors are grateful to Mylan laboratories Limited, Hyderabad, India, for the generous gift samples of acetaminophen and excipients.

Use of hydroxypropyl methylcellulose acetate succinate in an enteric polymer matrix to design controlled-release tablets of amoxicillin trihydrate.

Swelling Studies The swelling of the polymers upon hydration by the test medium was determined by a method similar to the equilibrium weight gain method as reported earlier To study the effect of enteric polymer type on the release profile of the drug from the matrix system.

The increase in polymer concentration resulted in an increase of the MDT values, where for mg polymer concentration the MDT value was 4. The non-Fickian release or anomalous transport of drug occurred when the n values are between the limiting values of Fickian and case II transport. Data sheets for overmetals, plastics, ceramics, and composites.

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Drug Dev Ind Pharm. Devi N, Maji TK. A composite polyelectrolytic matrix for controlled oral drug delivery.

Published online Jan To study the effect of anionic and cationic polymer ratio and polymer concentration on the release profile of the drug from the matrix system.

Kinetic Analysis of Release Data To describe the kinetics of drug release from the selected matrix formulation F8release data was analyzed according to different kinetic equations. Click here to view all the property values for this datasheet as they were originally entered into MatWeb. The rate of swelling was found to be different for different polymer combinations, and this could be attributed to the different drug release profiles and mechanisms observed during the dissolution analysis of matrix tablets.

Chemical structure of a EL and b EE polymer. At eudragih time intervals, the baskets containing the matrix tablets were removed, lightly blotted with tissue paper so as to remove excess water and weighed again. These baskets were then immersed in ml of pH 6. This slower drug release performance could be attributed to the PEC formation at this pH. A novel concept in enteric coating: