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Controlled release of active substance after double loading of demineralized cancellous bone

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dc.contributor.author Cobzac, Vitalie
dc.contributor.author Jian, Mariana
dc.contributor.author Maritoi, Tatiana
dc.contributor.author Baranețchi, Iana
dc.contributor.author Malcova, Tatiana
dc.contributor.author Nacu, Viorel
dc.date.accessioned 2025-05-12T07:13:32Z
dc.date.available 2025-05-12T07:13:32Z
dc.date.issued 2025
dc.identifier.citation COBZAC, Vitalie; Mariana JIAN; Tatiana MARITOI; Iana BARANETCHI; Tatiana MALCOVA AND Viorel NACU. Controlled release of active substance after double loading of demineralized cancellous bone. "Cells and Tissues Transplantation. Actualities and Perspectives", national scientific conference: the materials of the national scientific conference with internat. particip., the 3rd ed.: dedicated to the 80th anniversary of the founding of Nicolae Testemitanu State University of Medicine and Pharmacy. Chisinau, March 21-22, 2025: [abstracts]. Chişinău: CEP Medicina, 2025, p. 27. ISBN 978-9975-82-413-2. en_US
dc.identifier.isbn 978-9975-82-413-2
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/30502
dc.description.abstract Introduction. Demineralized bone graft (DBG) preparation involves substantial growth factor loss due to prolonged liquid exposure during demineralization, marrow and fat removal, and pH restoration. Albumins bind various endogenous substances and drugs in blood, and their incorporation into demineralized bone enhances regeneration. This study investigates the controlled release of biologically active substances from primary DBM loading after secondary bovine serum albumin (BSA) impregnation. Materials and methods: Demineralized cancellous bone was obtained from bovine iliac bone using 0.5 M HCl and processed per Human Tissue Bank protocols. To assess controlled release, primary coating was performed using Methylene Blue (MB) 10X solution (BioGnost, Croatia). Thirteen DBG samples were vacuumed at 400 mBar, then immersed in 150 ml of 325 µg/ml MB. Four groups were established based on secondary loading: (1) Positive control (MB+dH2O), (2) MB+10%BSA, (3) MB+20%BSA, and (4) Negative control (MB only). DBG weights did not significantly differ across groups (p > 0.2). After secondary vacuum loading with BSA, samples were frozen at -80°C and freezedried. MB release was assessed during 33 days by spectrophotometry at 570 nm (BioTek Instruments, USA). Results and Conclusions. The MB release differed significantly (p<0.05) between control groups from 4 hours to day 8, with higher release in the negative control. After this period, no significant difference was observed (p>0.05). Compared to the positive control, MB release in experimental groups did not differ within the first 6 hours (MB+10%BSA) or 21 hours (MB+20%BSA) (p>0.05). However, from this point until day 6, MB release was significantly higher in the positive control (p<0.05) before declining (p>0.05). MB release in the negative control was significantly higher than in experimental groups for the first 11 days (p<0.05), with no significant differences observed across groups from day 11 to day 33 (p>0.05) (Fig. 1). en_US
dc.language.iso en en_US
dc.publisher CEP Medicina en_US
dc.relation.ispartof Cells and tissues transplantation. Actualities and perspectives. The 3-rd edition. Chisinau, March 21-22, 2025 en_US
dc.subject controlled release en_US
dc.subject active substance en_US
dc.subject double loading en_US
dc.subject demineralized cancellous bone en_US
dc.title Controlled release of active substance after double loading of demineralized cancellous bone en_US
dc.type Other en_US


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