Fibrous membranes of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) with ceftriaxone: An investigation focused on wound healing applications
Antônio Schandler Ferri
, Maria Eduarda Araújo Ribeiro, Marina Rangel Ferro Pereira
, Fabrício Moreira Almeida, Theresa de Moura Monteiro, Fernanda Antunes
, Jose Gregório Cabrera Gomez
, Ruben J. Sanchez Rodriguez
, Maria Eduarda Araújo Ribeiro, Marina Rangel Ferro Pereira
, Fabrício Moreira Almeida, Theresa de Moura Monteiro, Fernanda Antunes
, Jose Gregório Cabrera Gomez
, Ruben J. Sanchez Rodriguez
Vol. 20., No.10., Pages 1089-1103, 2026
DOI: 10.3144/expresspolymlett.2026.79
DOI: 10.3144/expresspolymlett.2026.79
GRAPHICAL ABSTRACT

ABSTRACT
Conventional wound dressings, such as gauze, primarily act as physical barriers and provide limited support for tissue regeneration. In this study, electrospun poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (P(3HB-co-3HHx)) membranes were developed as multifunctional wound dressings combining a biomimetic fibrous structure with localized antibiotic delivery. Pristine and ceftriaxone (CFX)-loaded membranes were fabricated by electrospinning (15 kV, 1 mL/h, 20 cm, 6 h), yielding membranes approximately 300 μm thick. SEM revealed an interconnected fibrous architecture resembling the skin extracellular matrix, with mean fiber diameters of 1.38 ± 0.48 and 1.45 ± 0.57 μm for pristine and CFX-loaded membranes, respectively. Both membranes exhibited suitable wettability, water vapor transmission, and water sorption, while CFX incorporation reduced the water contact angle by approximately 17°, producing a less hydrophobic surface. CFX localization on the fiber surface resulted in an initial burst release, followed by diffusion-controlled release over 120 h. The membranes showed favorable in vitro and in vivo biological performance, with no cytotoxic effects and enhanced wound closure compared with commercial dressings. Overall, P(3HB-co-3HHx)/CFX membranes show potential as bioactive wound dressings combining extracellular-matrix-like architecture and localized antibiotic delivery.
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