AI Article Synopsis

  • Nisin, a natural food preservative, has limited use in biomedicine due to environmental fragility, prompting researchers to create a nanoparticle-hydrogel system to enhance its stability and release.
  • The study identified the nisin nanoparticles' desirable characteristics and selected chitosan-based hydrogels that can quickly gel and maintain a strong structure for optimal performance.
  • This composite system showed effective antibacterial properties, comparable to nisin alone, and exhibited excellent biocompatibility, making it a promising option for short-term wound dressings in medical applications.

Article Abstract

As a natural preservative, nisin is widely used in the food industry, while its application in biomedicine is limited due to its susceptibility to interference from external conditions. In this study, a nanoparticle-hydrogel composite system was designed to encapsulate and release nisin. Nisin nanoparticles were identified with a smooth, spherical visual morphology, particle size of 122.72 ± 4.88 nm, polydispersity coefficient of 0.473 ± 0.063, and zeta potential of 23.89 ± 0.37 mV. Based on the sample state and critical properties, three temperature-sensitive hydrogels based on chitosan were ultimately chosen with a rapid gelation time of 112 s, outstanding reticular structure, and optimal swelling ratio of 239.05 ± 7.15%. The composite system exhibited the same antibacterial properties as nisin, demonstrated by the composite system's inhibition zone diameter of 17.06 ± 0.83 mm, compared to 20.20 ± 0.58 mm for nisin, which was attributed to the prolonged release effect of the hydrogel at the appropriate temperature. The composite system also demonstrated good biocompatibility and safety, making it suitable for application as short-term wound dressings in biomedicine due to its low hemolysis rate of less than 2%. In summary, our nanoparticle-based hydrogel composite system offers a novel application form of nisin while ensuring its stability, thereby deepening and broadening the employment of nisin.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11433214PMC
http://dx.doi.org/10.3390/md22090428DOI Listing

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