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

Excipients for direct compaction--an update.

Gerad K Bolhuis1, N Anthony Armstrong

  • 1Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, Groningen, The Netherlands. g.k.bolhuis@rug.nl

Pharmaceutical Development and Technology
|March 21, 2006
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

Compaction properties of isomalt.

European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V·2009
Same author

Polyols as filler-binders for disintegrating tablets prepared by direct compaction.

Drug development and industrial pharmacy·2009
Same author

Hollow filler-binders as excipients for direct compaction.

Pharmaceutical research·2003
Same author

Inulin as filler-binder for tablets prepared by direct compaction.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences·2002
Same journal

<i>Camellia sinensis</i> Silver Nanoparticles Inhibit Proliferation and Induce PARP-Dependent Apoptosis in A549 Cells: Formulation, Characterization, and Biological Evaluation.

Pharmaceutical development and technology·2026
Same journal

Enhanced solubility and bioavailability of zanubrutinib nanocrystals: Physicochemical and Pharmacokinetic evaluation.

Pharmaceutical development and technology·2026
Same journal

Intradermal delivery of lidocaine hydrochloride using dissolving microneedles: <i>In vitro</i> dermatokinetic test and <i>in vivo</i> anesthetic activity assessment.

Pharmaceutical development and technology·2026
Same journal

Quality by design-guided development of silica-enabled lipid hybrid nanoparticles for enhanced olaparib dissolution.

Pharmaceutical development and technology·2026
Same journal

Surface engineering of nanocarriers with polymer coatings: materials, strategies, functional outcomes, and clinical translation.

Pharmaceutical development and technology·2026
Same journal

Compression equations in pharmaceutical tableting: from classical compaction models to data-driven and mechanistic approaches.

Pharmaceutical development and technology·2026
See all related articles

This review updates the 1996 assessment of excipients for direct tablet compaction. It covers new single-component and coprocessed filler-binders and advances in understanding their optimal design and function.

Area of Science:

  • Pharmaceutical Sciences
  • Materials Science

Background:

  • The direct compaction of tablets is a critical pharmaceutical manufacturing process.
  • A foundational review of excipients for direct compaction was published in 1996 by Bolhuis and Chowhan.
  • Significant advancements have occurred in the field since the initial review.

Purpose of the Study:

  • To provide an updated review of excipients utilized in direct tablet compaction.
  • To highlight new developments in single-component and coprocessed filler-binders.
  • To discuss recent progress in understanding the mechanisms and optimal design of these excipients.

Main Methods:

  • Literature review of scientific publications and industry reports.
  • Analysis of new excipient introductions and their properties.

Related Experiment Videos

  • Synthesis of current understanding regarding excipient functionality in direct compaction.
  • Main Results:

    • Introduction of novel single-component and coprocessed filler-binders.
    • Enhanced comprehension of the functional mechanisms of excipients during compaction.
    • Development of strategies for optimizing excipient design for improved tablet properties.

    Conclusions:

    • The field of direct compaction excipients has seen substantial innovation.
    • A deeper understanding of excipient science facilitates the development of superior materials.
    • Optimized excipient design is key to efficient and effective tablet manufacturing.