- Issue
- Journal of Siberian Federal University. Biology. 2026 19 (2)
- Authors
- Dudaev, Aleksey E.; Turchin, Vladimir I.
- Contact information
- Dudaev, Aleksey E. : Institute of Biophysics SB RAS Federal Research Center “Krasnoyarsk Science Center SB RAS” (Krasnoyarsk, Russian Federation); Siberian Federal University (Krasnoyarsk, Russian Federation); ; ORCID: 0000-0003-4873-126X; Turchin, Vladimir I. : Siberian Federal University (Krasnoyarsk, Russian Federation)
- Keywords
- degradable polyhydroxyalkanoates; films; laser irradiation; microrelief; 3D microscopy
- Abstract
Laser modification of biodegradable polyhydroxyalkanoate (PHA) films is a promising approach to tailoring their surface properties for biomedical applications. However, the quantitative relationship between polymer composition and the resulting 3D surface topography remains poorly understood. In this study, we use high-resolution 3D microscopy to evaluate the effects of CO2 laser treatment – under both continuous and quasi-pulsed modes – on films composed of four distinct PHAs: the homopolymer poly(3-hydroxybutyrate) [P(3HB)] and three copolymers – poly(3-hydroxybutyrate-co-3-hydroxyvalerate) [P(3HB-co-3HV)], poly(3-hydroxybutyrate- co-4-hydroxybutyrate) [P(3HB-co-4HB)], and poly(3- hydroxybutyrate-co-3-hydroxyhexanoate) [P(3HB-co-3HHx)]. Non-destructive 3D topographic mapping enabled precise quantification of groove and crater depths and uniformity. The homopolymer P(3HB) formed shallow (26.5 μm), fragmented structures, while copolymers, especially P(3HB-co-3HHx), produced deeper (up to 45.1 μm) and more uniform features, correlating with lower crystallinity and melting points. This study establishes 3D microscopy as an essential tool for quantitatively linking PHA composition to laser-induced microarchitecture, facilitating a rational design of degradable films with controlled topography
- Pages
- 325–332
- EDN
- UQBXES
- Paper at repository of SibFU
- https://elib.sfu-kras.ru/handle/2311/159249
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).