AI Article Synopsis

  • - The study focuses on improving the delivery of letrozole (LTZ), an anticancer drug, by directly adsorbing it onto clinoptilolite (CLI) zeolite, enhancing its dissolution in an acidic environment to increase bioavailability.
  • - After 23 hours, LTZ dissolved at a rate of 95% when associated with CLI zeolites, outperforming the dissolution rate of pure LTZ due to better exposure on the zeolite surface.
  • - The slight positive adsorption energy of CLI/LTZ (0.06 eV) indicates an effective and favorable release of LTZ in water, showcasing the potential for developing efficient drug delivery systems with improved action speed and bioavailability.

Article Abstract

High dissolution of anticancer drugs directly adsorbed onto porous carriers is indispensable for the development of drug delivery systems with high bioavailability. We report direct adsorption/loading of the anticancer drug letrozole (LTZ) onto the clinoptilolite (CLI) zeolite after the surface activation.In vitroLTZ dissolution from the CLI zeolites reached 95 % after 23 h in an acidic medium, being faster than the dissolution of the pure LTZ molecules. Fast dissolution occurs due to uniform exposure of the LTZ onto the external surface of the CLI zeolites, being accessible to the solvent for dissolution. On the other hand, the LTZ molecules were hidden in the bulk phase, giving a slow dissolution rate. Small positive value of the CLI/LTZ adsorption energy of 0.06 eV suggests that the release process is favourable in aqueous media. The main merit of the CLI/LTZ system is its quick onset of action and high bioavailability. This work demonstrates a possibility of enhancement of the dissolution of poorly soluble LTZ from the CLI zeolite, being promising for the further development of drug delivery systems.

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Source
http://dx.doi.org/10.1016/j.jcis.2023.08.199DOI Listing

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