PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 20, 2026ACS Omega0 citationsOpen Access

Zinc-Based bioMOF Nanocarrier for Curcumin Release Enables Permeation through Biomimetic Biological Membranes and Controlled Release

LCLorrayne Ohana CoelhoMPMarcos Vinícius de Sousa PereiraTATatianny de Araújo Andrade

Key Points

  • The aim is to enhance the delivery and bioavailability of curcumin using a zinc-based metal-organic framework as a nanocarrier.
  • Developed a zinc-based bio-MOF for curcumin loading and release.
  • Characterized by P-XRD, FT-IR, SEM-EDS, and TG/dTG.
  • Conducted in vitro cytotoxicity assays on MCF-7 cell lines and permeability studies.
  • Curcumin loading efficiency was 75.98 ± 2.65% (n=3).
  • Cytotoxicity assays showed reduced cell viability with the bio-MOF compared to free curcumin.
  • Release kinetics followed the Ritger-Peppas model with R²=0.948, indicating controlled release.

Abstract

High Resolution Image Download MS PowerPoint Slide Curcumin (Cur) is a natural polyphenolic compound with significant therapeutic potential, including antioxidant and anti-inflammatory activities. However, its clinical application is limited by its low aqueous solubility and low bioavailability. In this study, we developed a biocompatible Zn-based metal–organic framework (bio-MOF) as a nanocarrier for curcumin. The synthesized material was characterized by powder X-ray diffraction (P-XRD), fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS), and thermogravimetric analysis (TG/dTG), confirming the stability of the structure and the successful loading of the drug. The system showed a Cur loading efficiency of 75.98 ± 2.65% ( n = 3). Cytotoxicity assays were performed in MCF-7 cell lines and demonstrated that the delivery system has a superior effect on reducing cell viability compared to free cur. The release kinetics followed a Ritger-Peppas model ( R 2 = 0.948), indicating controlled release behavior. In vitro permeation studies revealed that the carrier successfully penetrated the biomimetic barrier and released Cur in the receptor compartment. Finally, through albumin fluorescence quenching analysis, a progressive decrease in fluorescence was observed with a Stern–Volmer constant ( K SV ) of 9.4 × 10 3 M –1, indicating a moderate binding affinity and suggesting that the nanocarrier can effectively interact with transport proteins. These findings demonstrate that the bio-MOF platform is a promising strategy to enhance the release and biological interaction of hydrophobic phytochemicals.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Coelho et al. (2026) studied this question.

synapsesocial.com/papers/6a5dba3f8bd453d3397ab823https://doi.org/10.1021/acsomega.6c00840
Ask AI
Helpful
Bookmark
Share
View Full Paper