Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Hydrodynamic flows around tablets in different pharmacopeial dissolution tests.

M Morihara1, N Aoyagi, N Kaniwa

  • 1National Institute of Health Sciences, 1-18-1 Kamiyoga, Setagaya-Ku, Tokyo 158-8501, Japan.

Drug Development and Industrial Pharmacy
|August 2, 2002
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Deciphering the Third Phase Structure in Uranium Extraction with Aliphatic Amines Using Combined Small-Angle X-ray and Neutron Scattering.

The journal of physical chemistry. B·2025
Same author

Repeated haemorrhages in peripheral nerve sheath tumours of the salivary glands after minor injury.

The British journal of oral & maxillofacial surgery·2017
Same author

Intra- and postoperative low-dose ketamine for adolescent idiopathic scoliosis surgery: a randomized controlled trial.

Acta anaesthesiologica Scandinavica·2015
Same author

Turn-over orbital septal flap and levator recession for upper-eyelid retraction secondary to thyroid eye disease.

Eye (London, England)·2013
Same author

ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease.

The pharmacogenomics journal·2011
Same author

A whole-genome association study of major determinants for allopurinol-related Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese patients.

The pharmacogenomics journal·2011

Hydrodynamic flow varies significantly across different dissolution tests, impacting drug release. Understanding these differences is crucial for accurate in vitro-in vivo correlations and quality control.

Area of Science:

  • Pharmaceutical Sciences
  • Chemical Engineering
  • Biomedical Engineering

Background:

  • Dissolution testing is critical for predicting in vivo drug performance.
  • Hydrodynamic conditions significantly influence drug release rates.
  • Pharmacopeial methods exhibit distinct hydrodynamic profiles.

Purpose of the Study:

  • To investigate and compare hydrodynamic flow patterns across various pharmacopeial dissolution tests.
  • To correlate hydrodynamic differences with drug dissolution behavior.
  • To inform the selection of appropriate dissolution methods for quality control and in vitro-in vivo studies.

Main Methods:

  • Utilized United States Pharmacopeial salicylic acid calibrators to determine hydrodynamic flow.
  • Compared rotating basket (RB), paddle (PD), flow-through cell (FT), and disintegration (DI) tests.

Related Experiment Videos

  • Analyzed dissolution rates and flow patterns around tablets.
  • Main Results:

    • Flow-through cell (FT) demonstrated lower hydrodynamic flow; disintegration (DI) showed higher flow.
    • Paddle (PD) and rotating basket (RB) tests exhibited similar flow at equal speeds, but different flow patterns.
    • Dissolution from the lower tablet surface was slower in the paddle (PD) method, potentially improved by sinkers.

    Conclusions:

    • Hydrodynamic differences among dissolution tests can explain variations in drug release profiles.
    • Consideration of these hydrodynamic variations is essential for selecting dissolution tests for in vitro-in vivo correlation and quality control.
    • The study highlights the importance of matching in vitro test conditions to intended in vivo performance.