# Mechanical tunability of oriented and random electrospun poly(ε-caprolactone) scaffolds via concentration, molecular weight, and environment

**Authors:** Muhammad A. Munawar, Dirk W. Schubert, Fritjof Nilsson

PMC · DOI: 10.1038/s41598-026-45961-9 · 2026-03-27

## TL;DR

This paper presents a framework for tuning the mechanical properties of electrospun PCL scaffolds by adjusting factors like polymer concentration, molecular weight, and fiber orientation.

## Contribution

The study integrates multiple tunable parameters into a single framework to achieve a broad mechanical window for PCL scaffolds.

## Key findings

- Oriented fibers show higher stiffness and tensile strength compared to randomly deposited fibers.
- Environmental exposure, such as acidic treatments, can reduce scaffold stiffness in a concentration- and temperature-dependent manner.

## Abstract

Achieving precise mechanical control in electrospun fibrous scaffolds remains a critical challenge for tissue engineering, where scaffold stiffness, strength, and extensibility must be tailored to diverse biological environments. Here, we establish a systematic framework for tuning the mechanical behavior of electrospun poly(ε-caprolactone) (PCL) fibers by integrating molecular-weight blending, polymer concentration control, fiber orientation, and environmental exposure within a single study. High-molecular-weight PCL (H-PCL) and blends with low-molecular-weight PCL (L-PCL) were electrospun to produce fibers with controlled diameters, morphologies, and orientations. Fiber alignment emerged as the dominant structural factor governing mechanical performance: oriented fibers exhibited substantially higher stiffness (~ 90–140 MPa) and tensile strength (up to ~ 100 MPa), while randomly deposited fibers showed markedly greater extensibility (up to ~ 1000%). Polymer concentration and resulting fiber diameter further modulated stiffness, with optimal mechanical performance observed at intermediate concentrations (~ 10–12% w/v). Molecular-weight blending provided an additional route to tailor fiber morphology and modulus, with oriented fibers reaching peak stiffness at ~ 50–60% H-PCL. Environmental exposure studies revealed that acidic treatments (formic and acetic acid solutions) reduce stiffness in a concentration- and temperature-dependent manner, whereas physiological soaking in phosphate-buffered saline (PBS, 37 °C) largely preserves scaffold integrity. Collectively, the electrospun scaffolds developed here span a broad mechanical window (~ 5–140 MPa). When positioned against literature-reported electrospun PCL scaffolds for cardiac, bone, and muscle tissue engineering, this range bridges multiple application-relevant stiffness regimes. These results provide a unified structure–property framework for designing mechanically tunable PCL fibrous scaffolds across diverse biomedical applications.

## Linked entities

- **Chemicals:** formic acid (PubChem CID 284), acetic acid (PubChem CID 176), phosphate-buffered saline (PubChem CID 24978514)

## Full-text entities

- **Genes:** PHF1 (PHD finger protein 1) [NCBI Gene 5252] {aka MTF2L2, PCL1, TDRD19C, hPHF1}
- **Diseases:** H-PCL (MESH:C566082), inflammatory (MESH:D007249)
- **Chemicals:** Mn (MESH:D008345), Polymer (MESH:D011108), Ca2+ (-), EtOH (MESH:D000431), Poly(epsilon-caprolactone) (MESH:C016240), Chloroform (MESH:D002725), acid (MESH:D000143), polyester (MESH:D011091), acetic (MESH:D019342), Gold (MESH:D006046), ester (MESH:D004952), FA (MESH:D005492), H2O (MESH:D014867), aluminum (MESH:D000535), Formic acid (MESH:C030544), formic acids (MESH:D005561)
- **Mutations:** Q150T, C) for 7, C) for 24, C in 5

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13031281/full.md

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Source: https://tomesphere.com/paper/PMC13031281