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

Polyanhydrides. V. Branched polyanhydrides.

M Maniar1, X D Xie, A J Domb

  • 1Nova Pharmaceutical Corporation, Baltimore, MD 21224-2788.

Biomaterials
|November 1, 1990
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

From hydroxychloroquine to ivermectin: what are the anti-viral properties of anti-parasitic drugs to combat SARS-CoV-2?

Journal of travel medicine·2021
Same author

[Effects of surgical and endovascular treatment of blood blister-like aneurysms of the internal carotid artery].

Zhonghua wai ke za zhi [Chinese journal of surgery]·2017
Same author

A phase II/III randomized study to compare the efficacy and safety of rigosertib plus gemcitabine versus gemcitabine alone in patients with previously untreated metastatic pancreatic cancer.

Annals of oncology : official journal of the European Society for Medical Oncology·2016
Same author

A phase II/III randomized study to compare the efficacy and safety of rigosertib plus gemcitabine versus gemcitabine alone in patients with previously untreated metastatic pancreatic cancer.

Annals of oncology : official journal of the European Society for Medical Oncology·2015
Same author

A phase II/III randomized study to compare the efficacy and safety of rigosertib plus gemcitabine versus gemcitabine alone in patients with previously untreated metastatic pancreatic cancer.

Annals of oncology : official journal of the European Society for Medical Oncology·2015
Same author

Extended duration local anesthetic agent in a rat paw model.

International journal of pharmaceutics·2014
Same journal

Corrigendum to "Photodynamic therapy produces enhanced efficacy of antitumor immunotherapy by simultaneously inducing intratumoral release of sorafenib" [Biomaterials 2020, 240, 119845].

Biomaterials·2026
Same journal

Mg-integrated octopus-inspired hydrogel dressing enables autonomous adhesion and wound closure for enhanced healing via sequential microenvironment regulation.

Biomaterials·2026
Same journal

Engineering miRNA-223 nanocomplexes via bioorthogonal self-assembly for precision therapy of intervertebral disc degeneration.

Biomaterials·2026
Same journal

Corrigendum to "Enhanced fluorescence imaging guided photodynamic therapy of sinoporphyrin sodium loaded graphene oxide" [Biomaterials 42 (2015) 16442].

Biomaterials·2026
Same journal

An injectable Ce-MnCo LDH nanozyme gel with cascade catalytic activity for acute radiation proctitis in rats.

Biomaterials·2026
Same journal

Peptide coacervate-mediated siRNA delivery for dual PD-1/PD-L1 blockade to enhance colorectal cancer immunotherapy.

Biomaterials·2026
See all related articles

Branched polyanhydrides exhibit higher molecular weights and faster degradation than linear polymers. Drug release profiles varied, with poly(acrylic acid) branched polymers showing higher initial release, but overall approaching linear polymer behavior.

Area of Science:

  • Polymer Chemistry
  • Materials Science
  • Biomaterials

Background:

  • Polyanhydrides are a class of biodegradable polymers with potential applications in drug delivery.
  • Branching can significantly alter polymer properties, including molecular weight, degradation, and drug release kinetics.

Purpose of the Study:

  • To synthesize and characterize branched polyanhydrides using sebacic acid with 1,3,5 benzenetricarboxylic acid and poly(acrylic acid) as branching agents.
  • To compare the physico-chemical properties, degradation behavior, and drug release profiles of branched polyanhydrides with their linear counterparts.

Main Methods:

  • Synthesis of random and graft-type branched polyanhydrides via polymerization.
  • Evaluation of molecular weight, specific viscosity, physico-chemical properties, and thermal behavior.

Related Experiment Videos

  • Assessment of degradation rates and drug release kinetics using morphine as a model drug.
  • Main Results:

    • Branched polyanhydrides achieved significantly higher molecular weights (250,000 Da) compared to linear poly(sebacic anhydride) (80,000 Da).
    • Branched polyanhydrides showed faster, triphasic degradation rates than linear polymers.
    • Morphine release was generally lower from branched polyanhydrides, with poly(acrylic acid) branched polymers exhibiting higher initial release.

    Conclusions:

    • Branching effectively increases polyanhydride molecular weight without significantly altering thermal or physico-chemical properties.
    • Branched polyanhydrides demonstrate altered degradation and drug release profiles compared to linear analogs.
    • The choice of branching agent influences drug release, offering tunable properties for specific applications.