Journal
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY
Volume 81, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.jddst.2023.104283
Keywords
Covalent organic framework; MCM-41; Drug delivery system; Antibacterial activity; Erythromycin
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The study focuses on a new drug delivery system for erythromycin using a covalent organic framework-based nanohybrid with desirable loading capacity and controlled release rate. The drug was incorporated using an environmentally friendly, economical, and easy-to-execute melting method. The nanohybrid demonstrated prolonged drug release and potent antibacterial activity against Staphylococcus aureus.
The present study focuses on a covalent organic framework-based (COF) nanohybrid as a new drug delivery system for erythromycin (E) antibiotic with a desirable loading capacity and controlled release rate. Solvent-free synthesis of PI-COF (polyimide-COF) plus pre-synthesized amino-functionalized MCM-41 resulted in a nano-hybrid structure of improved textural properties as a drug delivery system (DDS) with considerable biocom-patibility. The environmentally friendly, economical, and ease-execution melting method was employed for erythromycin incorporation in DDS. Results represent an increased loading efficiency of the pure covalent organic framework (86.86%) and the nanohybrid mode (56.2%) DDSs compared to other parallel structures reported. The release studies of erythromycin were performed in a simulated body environment (phosphate buffer solution (PBS) medium, pH = 7.4) at 37 +/- 1 degrees C. Furthermore, the antibiotic-loaded DDSs were investi-gated for antibacterial activity against Escherichia coli (E. coli), Pseudomonas aeruginosa (P. aeruginosa), and Staphylococcus aureus (S. aureus) strains. The E@nanohybrid attained a prolonged and sustained drug release (a maximum release of 69.7% for 50 h) and displayed potent antibacterial activity against Staphylococcus aureus. Zero and First-order, Higuchi, Hixson-Crowell, and Korsmeyer-Peppas kinetic models were applied to describe the release profile of erythromycin. Fitting mathematical models to the experimental data indicated Fickian and non-Fickian diffusion kinetics for nanohybrid sample and individual monomers, respectively.
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