# Preparation and Evaluation of an Oral Administration System of Albendazole-Metal-Organic Framework Based on Dual Response to pH and Enzymes

## TL;DR

This study creates a new drug delivery system for albendazole using metal-organic frameworks that respond to pH and enzymes, improving drug absorption and bioavailability in rats.

## Contribution

A novel pH- and enzyme-responsive oral drug delivery system for albendazole using metal-organic frameworks is developed and evaluated.

## Key findings

- ABZ@MOFs showed improved dissolution and oral bioavailability compared to free albendazole.
- ABZ@UiO-66-NH2 had 10.3-fold higher bioavailability than ABZ.
- The systems demonstrated structural stability in acidic environments and enzyme-triggered drug release.

## Abstract

Objective: This study aims to develop a metal–organic framework (ABZ-MOFs)-based oral drug delivery system for albendazole (ABZ) to enhance its dissolution rate and oral bioavailability. Methods: ABZ@MOF-802, ABZ@UiO-66-NH2, and ABZ@MIL-125-NH2 were synthesized using a solvothermal method, and their physicochemical properties were characterized. The in vitro drug release was investigated under pH- and enzyme-responsive conditions, followed by transmembrane transport studies in Caco-2 cells. Finally, the oral bioavailability of ABZ@MOFs was evaluated in rats. Results: The particle sizes of ABZ@MOF-802, ABZ@UiO-66-NH2, and ABZ@MIL-125-NH2 were (1062.6 ± 94.8), (228.3 ± 12.3), and (502.3 ± 16.2) nm, with drug loading efficiencies of (1.71 ± 0.08%), (12.13 ± 0.04%), and (26.17 ± 0.10%), respectively. The ABZ@MOFs demonstrated structural stability in acidic environments and released ABZ under weakly acidic and neutral conditions, exhibiting distinct release profiles in the presence of different enzymes. Cellular experiments confirmed that ABZ@MOFs significantly improved transmembrane drug absorption. Pharmacokinetic analysis revealed that the bioavailability of ABZ@UiO-66-NH2 and ABZ@MIL-125-NH2 was 10.3-fold and 1.8-fold higher, respectively, compared to ABZ. Conclusions: The ABZ@MOFs systems effectively improved ABZ dissolution and oral bioavailability, with ABZ@UiO-66-NH2 showing a dual response mechanism to pH and enzymes.