Alginate- and Chitosan-Modified Gelatin Hydrogel Microbeads for Delivery of E. coli Phages

Farzaneh Moghtader1,2,3, Sencer Solakoglu2, Erhan Piskin1,3

  • 1NanoBMT: Nanobiyomedtek Biyomedikal ve Biyoteknoloji San.Tic., Ltd. Sti., 48800 Köycegiz, Mugla, Turkey.

PubMed

Insights

Bacteriophages (phages) offer a promising alternative to antibiotics for combating resistant bacteria. This study developed novel gelatin microbeads to improve phage stability and control their release, creating user-friendly, long-lasting formulations.

Area of Science:

  • Biomaterials Science
  • Microbiology
  • Drug Delivery

Background:

  • Antibiotic resistance is a global health crisis, necessitating alternative treatments.
  • Bacteriophages (phages) are natural antibacterial agents with potential against resistant bacteria.
  • Developing stable and controlled-release phage formulations remains a significant challenge.

Purpose of the Study:

  • To develop gelatin hydrogel microbeads for bacteriophage encapsulation.
  • To investigate the effect of sodium alginate and chitosan on phage release and stability.
  • To create user-friendly, lyophilized phage formulations with extended shelf life.

Main Methods:

  • Two-step preparation of gelatin hydrogel microbeads, incorporating sodium alginate and chitosan coating.
  • Characterization of microbead properties: swelling ratio, diameter, Zeta potential, and acid degradation.
  • Encapsulation of T4 bacteriophage specific to Escherichia coli (E. coli) and evaluation of release kinetics.

Main Results:

  • Gelatin microbeads showed high initial phage release rates.
  • Incorporation of sodium alginate and chitosan significantly reduced phage release rates.
  • Gelatin-based microbead formulations, especially lyophilized ones, enhanced phage stability at room temperature.

Conclusions:

  • Gelatin hydrogel microbeads modified with alginate and chitosan offer controlled phage release.
  • These modified microbeads can lead to user-friendly, lyophilized phage formulations with improved stability and shelf life.
  • This approach presents a viable strategy for developing effective phage-based therapies against bacterial infections.

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