Fabrication and functionality of porous fibers prepared from microbial polyesters

Taizo Kabe, Taku Omura, Sakura Tsujimoto and Tadahisa Iwata

Winter 2026 Volume 42, No. 1 , 01-08

This study investigates microbially produced polyesters (polyhydroxyalkanoates, PHAs) derived from renewable resources. Drawn porous fibers were fabricated from P(3HB)-based copolymers with enhanced flexibility and processability, and their microstructures were systematically characterized. Synchrotron X-ray scattering and high-resolution 3D X-ray microscopy were employed to assess changes in higher-order structural features, including crystalline orientation, lamellar morphology, and porosity. The results indicate that fiber stretchability originates from reversible structural rearrangements. To explore potential medical applications, the ligation performance of the porous fibers was also evaluated. The fibers exhibited excellent handling characteristics, including self-ligation and the formation of smaller ligation sites, supporting their potential use as surgical sutures.

Highlights

  • Microbially produced P(3HB)-based copolymer fibers combine elasticity with controlled internal porosity through optimized processing, creating a biodegradable material with unique mechanical behavior.
  • Synchrotron X-ray scattering revealed that fiber elasticity arises from reversible rearrangement of crystalline lamellae and higher-order structures rather than irreversible crystal deformation.
  • Porous fibers demonstrated excellent knot security and formed substantially smaller knots through pore collapse, highlighting their potential for bioresorbable surgical suture applications.

Summary

Polyhydroxyalkanoates (PHAs) are biodegradable, bio-based polyesters produced by microorganisms from renewable resources. While these materials offer important sustainability advantages, their widespread use depends on improving processability and mechanical performance. Copolymerization of poly(3-hydroxybutyrate) with 4-hydroxybutyrate provides enhanced flexibility and drawability, enabling the production of elastic fibers with attractive structural and functional properties.

Detailed structural characterization using synchrotron wide-angle and small-angle X-ray scattering demonstrated that elasticity is governed by reversible changes in hierarchical structure. During stretching, crystalline orientation decreases, lattice spacing and lamellar long period increase, and these changes recover when the load is removed. Because these structural changes account for only part of the overall strain, deformation of amorphous regions and larger-scale hierarchical organization also plays a major role in elastic recovery.

Application of the microcrystal nucleation drawing process produced fibers containing a controlled network of internal pores. The size and distribution of these pores depended strongly on the low-temperature holding time during processing. Electron microscopy and high-resolution 3D X-ray microscopy showed that the pores deform during stretching while remaining largely discontinuous throughout the fiber.

The combination of elasticity and porosity provides practical functional advantages. During knot formation, elastic recovery tightens the knot while pore collapse allows significant compaction, producing smaller knots with improved knot security. These characteristics, together with the biodegradability and biocompatibility of the polymer system, make the material a promising candidate for future bioresorbable surgical sutures.

Frequently asked questions

PHAs are synthesized by microorganisms using renewable feedstocks such as sugars and plant oils and biodegrade into water and carbon dioxide through microbial action. They combine sustainability with thermoplastic processability and crystallinity, making them attractive alternatives to petroleum-derived plastics for applications where environmental impact and end-of-life disposal are important.

The elasticity is not produced by a conventional thermoplastic elastomer mechanism or block copolymer morphology. Instead, synchrotron X-ray analysis shows that elasticity originates from reversible changes in hierarchical structure, including crystalline orientation, lamellar spacing, and deformation of amorphous regions, all of which recover after unloading.

Real-time wide-angle and small-angle X-ray scattering allows structural evolution to be monitored while the fibers are stretched. These measurements reveal reversible changes in crystal orientation, lattice parameters, and lamellar long period, providing direct insight into how molecular-scale and nanoscale structural changes produce macroscopic elasticity.

The fibers are fabricated using a microcrystal nucleation drawing process. After melt spinning, the polymer is rapidly cooled below its glass transition temperature, held near that temperature for a controlled period, and then drawn. The holding time strongly influences pore formation, allowing the internal porous structure to be tailored.

The pores deform during stretching by increasing their aspect ratio while remaining largely discontinuous within the fiber. This pore deformation supplements the reversible deformation of the polymer's hierarchical structure, contributing to the overall extensibility without fundamentally changing the elastic recovery mechanism.

The combination of elasticity and controlled porosity improves knot performance. Elastic recovery helps tighten the knot automatically, while collapse of the internal pores reduces knot size. Smaller, more secure knots can lessen the amount of implanted material and potentially reduce tissue irritation while maintaining reliable fixation.

High-resolution laboratory X-ray computed tomography provides non-destructive visualization of the internal pore structure before and after knot formation. The technique clearly shows pore collapse within the knot while confirming that pores remain intact outside the compressed region, directly linking internal structural changes to functional performance.

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