Modeling and comparison of dissolution profiles.
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Summary
Drug dissolution from solid dosage forms has been described by kinetic models in which the dissolved amount of drug (Q) is a function of the test time, t or Q=f(t).
- Type
- review
- Published
- 2001-05-01
- Cited by
- 5,563
- References
- 80
- OpenAlex
- https://openalex.org/W2115439624
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:16454457
Keywords
Dissolution, Dissolution testing, Dosage form, Weibull distribution, Function (biology)
References
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- Effects of hardness on the disintegration time and the dissolution rate of uncoated caffeine tablets
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- Methods to compare dissolution profiles and a rationale for wide dissolution specifications for metoprolol tartrate tablets.
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- Statistical Evaluation of Similarity Factor f_2 as a Criterion for Assessment of Similarity Between Dissolution Profiles
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- Nanoscale eluting coatings based on alginate/chitosan hydrogels
- In vitro dissolution profile comparison of an anti-migraine combinational drug in dosage form.
- Incorporation of tocopherol acetate-containing particles in acrylic bone cement
- Synthesis, characterization and in vitro drug release of magnetic N-benzyl-O-carboxymethylchitosan nanoparticles loaded with indomethacin.
- Homogeneous diffusion layer model of dissolution incorporating the initial transient phase.
- Prediction of the human oral bioavailability by using in vitro and in silico drug related parameters in a physiologically based absorption model.
- Influence of pH Modifiers and HPMC Viscosity Grades on Nicotine–Magnesium Aluminum Silicate Complex-Loaded Buccal Matrix Tablets
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- Development and Characterization of Lyophilized Diazepam-Loaded Polymeric Micelles
- Design, Development, and Optimization of Polymeric Based-Colonic Drug Delivery System of Naproxen
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