Evidence map›Paper›PMID 41350714›Full record

ArticleBiomedical engineering online2025

Fabrication of testicular decellularized scaffolds using a hybrid SDS-supercritical CO₂ method: process optimization, extracellular matrix preservation, and biocompatibility evaluation.

Mojtaba Rastgou-Maeini, Ali Zeinolabedini Hezave, Seyed Hadi Anjamrooz, Fatemeh Hosseinpour, Ashraf Hassanpour-Dehnavi

Abstract read
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Article in Biomedical engineering online, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Mojtaba Rastgou-MaeiniTissue Engineering Lab., Anatomy Department, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Ali Zeinolabedini HezaveFanavari Atiyeh Pouyandegan Exir Company (APEX Technologies Co.), Science and Technology Park, Arak, Iran.
Seyed Hadi AnjamroozTissue Engineering Lab., Anatomy Department, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Fatemeh HosseinpourTissue Engineering Lab., Anatomy Department, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Ashraf Hassanpour-DehnaviTissue Engineering Lab., Anatomy Department, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran. a_hassanpour@sums.ac.ir.

Funding

Vice-Chancellor of Research in Shiraz University of Medical Sciences grant N. 27554
6 · The paper itself

Abstract

backgroundInfertility is a serious health issue that has social and economic impacts on families. The construction of a bioengineered testis as an alternative solution can enhance infertility treatment processes. The principles of tissue engineering are derived from the natural reconstruction and repair of tissues, where scaffolds, alongside cells and signaling molecules, play a key role. Therefore, the aim of this study is to prepare a decellularized testicular scaffold from mouse tissue based on a supercritical carbon dioxide protocol and to investigate its histological properties, cell viability, and compatibility.

methodsThe whole rat testis tissue was decellularized using 1% SDS as pretreatment, Ethanol 70% as Co-solvent and Supercritical Carbon Dioxide. Optimal acellular removal was confirmed through DNA content analysis and staining with Hematoxylin-Eosin. The preservation of extracellular matrix structures was evaluated through glycosaminoglycans (GAGs) extraction and histological staining techniques, including periodic acid-Schiff, aldehyde fuchsin, Alcian blue, Masson's trichrome, and Scanning electron microscopy (SEM). Additionally, the cytotoxicity of the scaffold was assessed using the MTT assay.

resultsThe optimal protocol for decellularization was determined to involve a combination of 1% SDS for 8 h and Supercritical Carbon Dioxide at parameters of 200 bar pressure, 45 °C, and a duration of 5 h. Evidence provided by quantitative and qualitative assessments of DNA, GAGs, SEM, and histochemical analyses confirmed effective cellular removal while adequately preserving the extracellular matrix of the rat testis post-decellularization. Additionally, the biocompatibility of the prepared scaffold was established through MTT assay, indicating favorable biological compatibility.

conclusionDespite the fact that the supercritical carbon dioxide protocol alone was unable to produce a decellularized scaffold with the desired standard characteristics, its combined use with 1% SDS not only reduced the decellularization time compared to other methods but also effectively preserved the extracellular matrix structures.

Indexed as

Biocompatible MaterialsCarbon DioxideDecellularized Extracellular MatrixExtracellular MatrixMaterials TestingSodium Dodecyl SulfateTestisTissue ScaffoldsAnimalsCell SurvivalGlycosaminoglycansMaleMiceRatsTissue EngineeringBiocompatible MaterialsCarbon DioxideDecellularized Extracellular MatrixGlycosaminoglycansSodium Dodecyl SulfateDecellularizationECM‑based scaffoldsscCO2TestisTissue engineering

Identifiers

PMID41350714
PMCPMC12681112

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.