In the realm of medical education and research, the preservation of anatomical specimens has traditionally relied on formaldehyde-based fixatives, posing challenges such as loss of 3D orientation, unpleasant odor, and tissue alterations during extended storage. A more contemporary approach introduced in the late 20th century is plastination, which replaces water and fat with durable polymers, providing odorless and stable specimens for ultra-long-term storage. Despite the success of plastination, its impact on subsequent histopathological studies, particularly regarding special stains and immunohistochemistry (IHC), remains largely unexplored. This study delves into assessing the feasibility of staining deplastinated osteochondral units (OCU). Employing a comprehensive multi-step methodology involving fixation, decalcification, plastination, deplastination, paraffin embedding, and various staining protocols, the study meticulously evaluates tissue integrity and staining outcomes using human OCU. Significantly, the plastinated and deplastinated OCUs exhibit well-preserved tissue morphology in Hematoxylin and Eosin staining, successful glycosaminoglycan staining with Safranin O, and effective visualization of collagen types II and X through IHC analysis. A noteworthy observation is the potential to stain plastinated bone-containing specimens after deplastination, addressing the drawbacks of long-term tissue preservation using formalin. This innovation allows subsequent staining as needed, and the direct handling of plastinated specimens enhances three-dimensional visualization, rendering them valuable tools in forensic examinations. These findings open promising avenues for refining methodologies in medical education and forensic settings. The establishment of reliable staining and deplastination protocols holds the potential to significantly improve result accuracy and reproducibility, ultimately expanding applications in these critical fields.
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