AI Article Synopsis

  • Targeted drug release involves using biocompatible polymer carriers to deliver medications effectively.
  • Researchers developed cryogenically structured carriers from alginate and chondroitin sulfate and assessed their properties and drug release capabilities.
  • The study found that the concentration and ratio of these polymers significantly influenced swelling and porosity, with chondroitin sulfate affecting the release rate of certain antibiotics like gentamicin while having minimal impact on others like dioxidine.

Article Abstract

Targeted drug release is a significant research focus in the development of drug delivery systems and involves a biocompatible polymeric carrier and certain medicines. Cryostructuring is a suitable approach for the preparation of efficient macroporous carriers for such drug delivery systems. In the current study, the cryogenically structured carriers based on alginate/chondroitin sulfate mixtures were prepared and their physicochemical properties and their ability to absorb/release the bactericides were evaluated. The swelling parameters of the polysaccharide matrix, the amount of the tightly bound water in the polymer and the sulfur content were measured. In addition, FTIR and UV spectroscopy, optical and scanning microscopy, as well as a standard disk diffusion method for determining antibacterial activity were used. It was shown that alginate/chondroitin sulfate concentration and their ratios were significant factors influencing the swelling properties and the porosity of the resultant cryostructurates. It was demonstrated that the presence of chondroitin sulfate in the composition of a polymeric matrix slowed down the release of the aminoglycoside antibiotic gentamicin. In the case of the NH-free bactericide, dioxidine, the release was almost independent of the presence of chondroitin sulfate. This trend was also registered for the antibacterial activity tests against the bacteria, when examining the drug-loaded biopolymeric carriers.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414213PMC
http://dx.doi.org/10.3390/polym14163271DOI Listing

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