(Q34215811)

31 July 2017

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title

Modeling and comparison of dissolution profiles (English)

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31 July 2017

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Costa P

1

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31 July 2017

Sousa Lobo JM

series ordinal

2

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31 July 2017

language of work or name

English

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publication date

1 May 2001

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European Journal of Pharmaceutical Sciences

31 July 2017

published in

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31 July 2017

volume

13

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31 July 2017

issue

2

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31 July 2017

page(s)

123-133

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Physical interpretation of parameters in the Rosin-Rammler-Sperling-Weibull distribution for drug release from controlled release dosage forms

31 July 2017

cites work

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Influence of Shape Factors on Kinetics of Drug Release from Matrix Tablets II: Experimental

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Investigation of factors influencing release of solid drug dispersed in inert matrices. 3. Quantitative studies involving the polyethylene plastic matrix

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Investigation of factors influencing release of solid drug dispersed in inert matrices. IV. Some studies involving the polyvinyl chloride matrix

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Investigation of factors influencing release of solid drug dispersed in inert matrices. II. Quantitation of procedures

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Dissolution properties of praziquantel--PVP systems

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Evaluation and comparison of dissolution data derived from different modified release dosage forms: an alternative method.

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Establishment of sink conditions in dissolution rate determinations. Theoretical considerations and application to nondisintegrating dosage forms

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Drug/polymer matrix swelling and dissolution

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Diffusion in porous materials above the percolation threshold

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Rate of Release of Medicaments from Ointment Bases Containing Drugs in Suspension

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MECHANISM OF SUSTAINED-ACTION MEDICATION. THEORETICAL ANALYSIS OF RATE OF RELEASE OF SOLID DRUGS DISPERSED IN SOLID MATRICES

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Analysis of data on the medicament release from ointments

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Effects of hardness on the disintegration time and the dissolution rate of uncoated caffeine tablets

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In vitro release modulation from crosslinked pellets for site-specific drug delivery to the gastrointestinal tract. I. Comparison of pH-responsive drug release and associated kinetics.

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Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets

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Drug release from wax matrices. I. Analysis of data with first-order kinetics and with the diffusion-controlled model

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7 January 2021

Drug release from wax matrices. II. Application of a mixture theory to the suflanilamide--wax system

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7 January 2021

Controlled release of 3',5'-diester prodrugs of 5-fluoro-2'-deoxyuridine from poly-L-lactic acid microspheres

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Effect of drug (core) particle size on the dissolution of theophylline from microspheres made from low molecular weight cellulose acetate propionate

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7 January 2021

Dissolution of fludrocortisone from phospholipid coprecipitates

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Interpretation of Percent Dissolved-Time Plots Derived from In Vitro Testing of Conventional Tablets and Capsules

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Identifiers

DOI

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31 July 2017

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