# Nano-Structural Characterization of Human Aponeurotic Tissue by Atomic Force Microscopy

## TL;DR

This study uses atomic force microscopy to explore the nano-scale structure of human aponeurotic tissue, revealing organized collagen fibers and surface variations.

## Contribution

The paper provides a baseline nano-scale characterization of macroscopically normal aponeurotic tissue using AFM, which is novel for this tissue type.

## Key findings

- AFM revealed a well-organized fibrillar architecture with preferential orientation in aponeurotic tissue.
- Deflection imaging showed spatial heterogeneity in contrast between collagen-dense and interfibrillar regions.
- Surface roughness parameters indicated a compact extracellular matrix without signs of disruption.

## Abstract

Background: The structural integrity of the abdominal wall is critically dependent on the organization of aponeurotic tissue, a dense collagen-rich connective structure responsible for directional force transmission. While the clinical relevance of the aponeurosis is well recognized in abdominal wall reconstruction, its nano-scale structural organization remains insufficiently characterized. Atomic force microscopy (AFM) provides a suitable approach for investigating surface morphology and nano-architectural features of biological tissues. Methods: Human aponeurotic tissue samples were analyzed using atomic force microscopy operated in contact-mode deflection and topography imaging. Two-dimensional and three-dimensional surface topographies were acquired at the micrometer scale to assess nano-architectural organization. Areal surface roughness parameters (Sa, Sq, Sp, Sv, Sy) were calculated to quantify morphological heterogeneity. AFM deflection imaging was used to evaluate relative spatial variations in deflection imaging contrast under the applied scanning conditions across collagen-dense and interfibrillar regions. Results: AFM analysis revealed a well-organized fibrillar architecture with preferential orientation, consistent with the anisotropic organization of aponeurotic connective tissue. Deflection images demonstrated spatial heterogeneity in deflection contrast at the scanned scale, reflecting variations in the tip–sample interaction signal between collagen-dense and interfibrillar regions. Surface topography showed a continuous morphology with moderate height variations and smooth transitions between structural elements. Roughness parameters reflected a compact extracellular matrix organization within the scanned areas, without features suggestive of surface disruption. Conclusions: Atomic force microscopy enables detailed nano-scale structural characterization of human aponeurotic tissue and reveals spatial heterogeneity in deflection imaging contrast under specific contact-mode scanning conditions. These findings provide a baseline nano-scale descriptive reference dataset for macroscopically normal aponeurotic tissue, supporting future comparative investigations without implying validated mechanical differences or direct tissue–implant interaction analysis within the present study.