Lignan dinitrohinokinin displays important biological activities, which led to the preparation of its poly-ε-caprolactone nanoparticles. Kinetics analysis revealed initially slow drug release followed by a prolonged, moderate release 6 h later due to DNHK diffusion through the polymeric matrix. Molecular dynamics simulations show that DNHK molecules that interact stronger with other DNHK molecules near the PCL/DNHK surface are more difficult to dissociate from the nanoparticle. The smaller diameter nanocapsules with negative surface charge conferred good colloidal stability. The formulations showed a size distribution with monodisperse systems formation. evaluation of schistosomicidal activity against showed that DNHK, when incorporated into nanoparticles, caused egg number reduction of 4.2% and 28.1% at 40 mg/kg and 94.2% and 84.4% at 400 mg/kg in the liver and the spleen, respectively. The PCL nanoparticles were stable in aqueous dispersion and could be optimized to be used as a promising lignan release agent.

Download full-text PDF

Source
http://dx.doi.org/10.1080/14786419.2021.2021515DOI Listing

Publication Analysis

Top Keywords

schistosomicidal activity
8
dnhk molecules
8
evaluation lignan-loaded
4
lignan-loaded polyε-caprolactone
4
nanoparticles
4
polyε-caprolactone nanoparticles
4
nanoparticles synthesis
4
synthesis characterization
4
characterization schistosomicidal
4
activity lignan
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!