Literature DB >> 19543816

Powder dissolution method for estimating rotating disk intrinsic dissolution rates of low solubility drugs.

Konstantin Tsinman1, Alex Avdeef, Oksana Tsinman, Dmytro Voloboy.   

Abstract

PURPOSE: The objective was to investigate the applicability and limitations of a novel approach for measuring intrinsic dissolution rates (IDR) of very small quantities of compounds introduced as powders to buffered solutions and comparing these results to disk IDR obtained using the traditional Wood's apparatus.
METHODS: The powder dissolution profiles of 13 model drugs were determined at 37 degrees C in USP buffers at pH 1.2, 4.5, and 6.8, stirred at 100 RPM. As little as 0.06 mg of drug were added to 1 mL buffer media. Drug concentration was measured by an in situ fiber optic UV method. The results were converted to rotating disk IDR values by a novel mathematical procedure.
RESULTS: The comparison of the powder-based IDR values to those obtained by traditional Wood's apparatus indicated r(2) = 0.97 (n = 26).
CONCLUSION: The results demonstrate that using potentially 10,000-fold less drug material does not sacrifice the quality of the measurement, and lends support to an earlier study that the disk IDR measurement may possibly serve as a surrogate for the BCS solubility classification.

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Year:  2009        PMID: 19543816     DOI: 10.1007/s11095-009-9921-3

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  21 in total

1.  Feasibility studies of utilizing disk intrinsic dissolution rate to classify drugs.

Authors:  Lawrence X Yu; Alan S Carlin; Gordon L Amidon; Ajaz S Hussain
Journal:  Int J Pharm       Date:  2004-02-11       Impact factor: 5.875

2.  Dissolution rates of finely divided drug powders. I. Effect of a distribution of particle sizes in a diffusion-controlled process.

Authors:  W I HIGUCHI; E N HIESTAND
Journal:  J Pharm Sci       Date:  1963-01       Impact factor: 3.534

3.  Experimental determination of the diffusion boundary layer width of micron and submicron particles.

Authors:  C Galli
Journal:  Int J Pharm       Date:  2006-03-09       Impact factor: 5.875

4.  Miniaturization of powder dissolution measurement and estimation of particle size.

Authors:  Alex Avdeef; Konstantin Tsinman; Oksana Tsinman; Na Sun; Dmytro Voloboy
Journal:  Chem Biodivers       Date:  2009-11       Impact factor: 2.408

5.  General class of multiparticulate dissolution models.

Authors:  P V Pedersen; K F Brown
Journal:  J Pharm Sci       Date:  1977-10       Impact factor: 3.534

6.  Dissolution of ionizable water-insoluble drugs: the combined effect of pH and surfactant.

Authors:  J Jinno; D m Oh; J R Crison; G L Amidon
Journal:  J Pharm Sci       Date:  2000-02       Impact factor: 3.534

7.  Dissolution modeling: factors affecting the dissolution rates of polydisperse powders.

Authors:  A T Lu; M E Frisella; K C Johnson
Journal:  Pharm Res       Date:  1993-09       Impact factor: 4.200

8.  Improved holder for intrinsic dissolution rate studies.

Authors:  J Wood; J Syarto; H Letterman
Journal:  J Pharm Sci       Date:  1965-07       Impact factor: 3.534

9.  A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability.

Authors:  G L Amidon; H Lennernäs; V P Shah; J R Crison
Journal:  Pharm Res       Date:  1995-03       Impact factor: 4.200

10.  Effect of diffusion layer pH and solubility on the dissolution rate of pharmaceutical bases and their hydrochloride salts. I: Phenazopyridine.

Authors:  A T Serajuddin; C I Jarowski
Journal:  J Pharm Sci       Date:  1985-02       Impact factor: 3.534

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  6 in total

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Journal:  Pharm Res       Date:  2012-06-12       Impact factor: 4.200

2.  Influence of particle size on the ultraviolet spectrum of particulate-containing solutions: implications for in-situ concentration monitoring using UV/Vis fiber-optic probes.

Authors:  Bernard Van Eerdenbrugh; David E Alonzo; Lynne S Taylor
Journal:  Pharm Res       Date:  2011-03-04       Impact factor: 4.200

3.  Attenuated total reflection-Fourier transform infrared spectroscopic imaging of pharmaceuticals in microfluidic devices.

Authors:  Andrew V Ewing; Graham S Clarke; Sergei G Kazarian
Journal:  Biomicrofluidics       Date:  2016-04-20       Impact factor: 2.800

4.  Controlled Suspensions Enable Rapid Determinations of Intrinsic Dissolution Rate and Apparent Solubility of Poorly Water-Soluble Compounds.

Authors:  Sara B E Andersson; Caroline Alvebratt; Christel A S Bergström
Journal:  Pharm Res       Date:  2017-06-15       Impact factor: 4.200

5.  The function of oxybuprocaine: a parachute effect that sustains the supersaturated state of anhydrous piroxicam crystals.

Authors:  Momoko Fujita; Satoru Goto; Hitoshi Chatani; Yuta Otsuka; Yohsuke Shimada; Hiroshi Terada; Katsuyuki Inoo
Journal:  RSC Adv       Date:  2020-01-08       Impact factor: 4.036

6.  Determination of Intrinsic Drug Dissolution and Solute Effective Transport Rate during Laminar Fluid Flow at Different Velocities.

Authors:  Sara B E Andersson; Göran Frenning; Göran Alderborn
Journal:  Pharmaceutics       Date:  2021-06-04       Impact factor: 6.321

  6 in total

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