4.3 Article

Long-term release of bioactive interferon-alpha from PLGA-chitosan microparticles: in vitro and in vivo studies

Journal

BIOMATERIALS ADVANCES
Volume 143, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.bioadv.2022.213167

Keywords

Porcine interferon alpha; Cytokine; Polymeric microparticle; Drug delivery; Poly (D; L-lactide-co-glycolide); Chitosan; FTIR; Spray-drying

Funding

  1. Corporacion de Fomento a la Produccion (CORFO-Chile) [17IDAE-74707]
  2. Agencia Nacional de Investigacion y Desarrollo (ANID-Chile: Fondecyt Postdoctoral) [3190261, 3190044, 3180694]

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In this study, porcine interferon-alpha (IFN alpha) was encapsulated in PLGA-chitosan microparticles to achieve slow drug release and protection. The procedure used to obtain IFN alpha-MPs was reproducible, and in vitro and in vivo experiments showed improved prophylactic and therapeutic potential, protecting the IFN alpha molecules and achieving sustained release for at least two weeks.
Effective cytokine treatments often require high-and multiple-dose due to the short half-life of these molecules. Here, porcine interferon-alpha (IFN alpha) is encapsulated in PLGA-chitosan microparticles (IFN alpha-MPs) to accomplish both slow drug release and drug protection from degradation. A procedure that combines emulsion and spray -drying techniques yielded almost spherical microspheres with an average diameter of 3.00 +/- 1.50 mu m. SEM, Microtrac, and Z-potential analyses of three IFN alpha-MP batches showed similar results, indicating the process is reproducible. These studies supported molecular evidence obtained in FTIR analysis, which indicated a compact structure of IFN alpha-MPs. Consistently, IFN alpha release kinetics assessed in vitro followed a zero-order behavior typical of sustained release from a polymeric matrix. This study showed that IFN alpha-MPs released bioactive molecules for at least 15 days, achieving IFN alpha protection. In addition, pigs treated with IFN alpha-MPs exhibited overexpression of IFN alpha-stimulated genes 16 days after treatment. Instead, the expression levels of these genes decreased after day 4th in pigs treated with non-encapsulated IFN alpha. In vitro and in vivo experiments demonstrated that the formu-lation improved the prophylactic and therapeutic potential of IFN alpha, accomplishing molecule protection and long-term release for at least two weeks. The procedure used to obtain IFN alpha-MPs is reproducible, scalable, and suitable for encapsulating other drugs.

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