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This review describes the different methodology involved in cytotoxicity, pathogenicity, immunogenicity and biodegradability testing for evaluating the biocompatibility of various decellularized matrices obtained from human or animals.
However, when evaluating the biocompatibility of a particular metal component, the results do not necessarily apply to all implants made of the same material.
Therefore, evaluating the biocompatibility of ZnO nanostructures is important.
The use of appropriate assessments is vital in evaluating the biocompatibility of MNPs.
Our study has important implications for evaluating the biocompatibility of nanocarriers and designing better and safer ones for drug delivery.
Cell attachment and spreading are crucial for cell growth and differentiation and therefore become vital factors when evaluating the biocompatibility of a biomaterial.
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To identify novel biocompatible materials for intravesical implanted medical devices, we evaluated the biocompatibility of polymethyl methacrylate (PMMA) by analyzing changes in the levels of macrophages, macrophage migratory inhibitory factor (MIF), and inflammatory cytokines in the bladder.
To evaluate the biocompatibility of PAMNPs, some experiments have been conducted.
The purpose of this paper was to evaluate the biocompatibility of PAMNPs, providing evidence for clinical benefits.
In order to evaluate the biocompatibility of the scaffolds, extracts and direct contact tests were performed.
MTT assay was done to evaluate the biocompatibility of these membranes using MG-63 osteosarcoma cells.
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