Abstract

Poly-ɛ-caprolactone (PCL) is now widely studied in relation to the engineering of bone, cartilage, tendons, and other tissues. Standard histological protocols can destroy the carefully created trabecular and honeycomb-like architecture of PCL scaffolds, and could lead to scaffold fibers swelling, resulting in the displacement or compression of tissues inside the scaffold. The aim of this study was to modify a standard histopathological protocol for PCL scaffold preparation and evaluate it on porous cylindrical PCL scaffolds in a rat model. In 16 inbred Wag rats, 2 PCL scaffolds were implanted subcutaneously to both inguinal areas. Two months after implantation, harvested scaffolds were first subjected to μCT imaging, and then to histopathological analysis with standard (left inguinal area) and modified histopathological protocols (right inguinal area). To standardize the results, soft tissue percentages (STPs) were calculated on scaffold cross-sections obtained from both histopathological protocols and compared with corresponding µCT cross-sections. The modified protocol enabled the assessment of almost 10× more soft tissues on the scaffold cross-section than the standard procedure. Moreover, STP was only 1.5% lower than in the corresponding µCT cross-sections assessed before the histopathological procedure. The presented modification of the histopathological protocol is cheap, reproducible, and allows for a comprehensive evaluation of PCL scaffolds while maintaining their trabecular, honeycomb-like structure on cross-sections.

Highlights

  • Poly--caprolactone (PCL) is a hydrophobic, semi-crystalline polymer which was synthesized in the 1930s [1]

  • The biocompatibility of the tested scaffolds was proven in our previous study on an The biocompatibility of the tested scaffolds was proven in our previous study on an animal model, where we found that adipose-derived stem cells (ASCs) seeded into PCL

  • Animal model, where we found that adipose-derived stem cells (ASCs) seeded into PCL

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Summary

Introduction

Poly--caprolactone (PCL) is a hydrophobic, semi-crystalline polymer which was synthesized in the 1930s [1]. The first stage is the non-enzymatic hydrolytic cleavage of ester groups, whereas the second is dependent upon polymer crystallinity and is described as intracellular degradation [2,3]. The in vitro degradation of PCL is followed by an increase in the polymer’s degree of crystallinity [4,5]. The increase in crystallinity is governed by crystalline fibril reorganization, which affects. PCL is nontoxic and has a suitable surface for cell proliferation and differentiation, and its non-toxic degradation products are usually metabolized and eliminated via natural pathways [6]

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