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

Incorporation of polymeric nanoparticles into solid dosage forms

C Schmidt1, R Bodmeier

  • 1College of Pharmacy, Freie Universität Berlin, Kelchstr. 31, 12169 Berlin, Germany.

Journal of Controlled Release : Official Journal of the Controlled Release Society
|February 11, 1999
PubMed
Summary

Oral polymeric nanoparticles are crucial for drug delivery. This study found that high minimum film formation temperature (MFT) and good wettability are key for nanoparticle redispersibility from solid dosage forms.

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

[Radiology in managed care environment: opportunities for cost savings in an HMO].

RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin·2003
Same author

[Quality management in surgery--an overview of methods and possibilities].

Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen·2003
Same author

[How are interstitial lung diseases diagnosed in Germany? Results of the scientific registry for the exploration of interstitial lung diseases ("Fibrosis registry") of the WATL].

Pneumologie (Stuttgart, Germany)·2003
Same author

IL-6 and PGE2 release by human osteoblasts on implant materials.

Biomaterials·2003
Same author

[Investors in the healthcare market].

Deutsche medizinische Wochenschrift (1946)·2003
Same author

Functional relevance of antiemetic control. Experience using the FLIE questionnaire in a randomised study of the NK-1 antagonist aprepitant.

European journal of cancer (Oxford, England : 1990)·2003

Area of Science:

  • Pharmaceutical Technology
  • Materials Science

Background:

  • Polymeric nanoparticles are increasingly utilized for oral drug delivery.
  • Their successful application depends on maintaining nanoparticle integrity upon release from solid dosage forms.

Purpose of the Study:

  • To investigate the compatibility of model polymeric nanoparticles with tabletting excipients.
  • To assess the redispersibility of nanoparticles from various solid dosage forms (granules, tablets, pellets, films).
  • To identify critical parameters influencing nanoparticle integrity after release.

Main Methods:

  • Incorporation of Eudragit(R) and Aquacoat(R) nanoparticle dispersions into solid dosage forms.
  • Evaluation of nanoparticle-binder interactions during wet granulation.
  • Assessment of nanoparticle redispersibility and particle size post-release.

Related Experiment Videos

  • Contact angle measurements to determine nanoparticle wettability.
  • Main Results:

    • Phase separation occurred in many nanoparticle/binder systems during wet granulation.
    • High minimum film formation temperature (MFT) and good wettability were critical for nanoparticle redispersibility.
    • Low MFT led to nanoparticle coalescence and poor redispersibility.
    • Contact angle correlated with redispersibility; Eudragit(R) RL showed good redispersibility with low contact angles.

    Conclusions:

    • Maintaining nanoparticle properties requires careful selection of polymers and excipients.
    • Minimum film formation temperature (MFT) and wettability are critical parameters for successful oral nanoparticle formulation.
    • Eudragit(R) RL demonstrates favorable characteristics for redispersibility in oral solid dosage forms.