What question did this study set out to answer?

The study aims to quantify retained donor nuclei in nerve wraps to evaluate decellularization efficiency and biocompatibility.

April 23, 2026

Quantification of Retained Donor Nuclei in ECM-Based Nerve Wraps: A Histological Assessment of Decellularization and Biocompatibility

Key Points

The study aims to quantify retained donor nuclei in nerve wraps to evaluate decellularization efficiency and biocompatibility.
Collection of commercially available nerve wrap samples
Histological assessment using hematoxylin and eosin (H&E) staining
Quantification of visible nuclei and cell-free fields under standardized fluorescence imaging
One reconstituted xenograft and a porcine placental product had >90% cell-free fields and <10 nuclei per field.
A native porcine small intestinal submucosa and a human amnion/chorion membrane retained >50 nuclei per field and 0% cell-free fields.
Significant variability in decellularization practices was observed among the nerve wraps.

Abstract

Background: Peripheral nerve injuries present a significant clinical challenge, often resulting in chronic pain, sensory loss, and motor dysfunction. Biologically derived nerve wraps are frequently used in surgical nerve repair to reduce adhesion, promote regeneration, and minimize fibrosis. These extracellular matrix-based biomaterials vary widely in composition and processing, including the extent of donor decellularization. Retained donor nuclei and cellular remnants have been implicated in triggering adverse immune responses, including chronic inflammation and fibrotic encapsulation. This study investigates the extent of retained nuclear material in commercially available nerve wraps to establish histological metrics for decellularization efficiency and potential biocompatibility. Methods: Samples of multiple commercially available nerve wraps were collected and prepared according to manufacturer specifications. Histological assessment was performed using hematoxylin and eosin (H&E) staining. Slides were analyzed at 20X magnification using a standardized fluorescence imaging system. Two primary endpoints were quantified: (1) the number of visible nuclei per three representative microscopic fields and (2) the percentage of cell-free fields per sample. Results: Substantial variability was observed among products. One reconstituted xenograft and a porcine placental product demonstrated complete decellularization with >90% cell-free fields and 50 nuclei per field and 0% cell-free fields. These findings suggest inconsistent decellularization practices across manufacturers. Conclusion: This study identifies significant differences in residual donor nuclear content among commercially available extracellular matrix nerve wraps. Histological quantification using H&E staining may serve as a reproducible method for assessing decellularization quality. These metrics may help predict immunologic compatibility and guide future biomaterial selection in peripheral nerve repair.

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