Evaluation of Different Commercial Sealing Hemostatic Patches for Their Selection as Reservoirs for Localized Intraperitoneal Chemotherapy

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dc.contributor.author Perelló-Trias, M.T.
dc.contributor.author Rodríguez-Fernández, A.
dc.contributor.author Serrano-Muñoz, A.J.
dc.contributor.author Segura-Sampedro, J.J.
dc.contributor.author Tauler, P.
dc.contributor.author Ramis, J.M.
dc.contributor.author Monjo, M.
dc.date.accessioned 2025-09-17T09:46:24Z
dc.date.available 2025-09-17T09:46:24Z
dc.identifier.citation Perelló-Trias, M.T., Rodríguez-Fernández, A., Serrano-Muñoz, A.J., Segura-Sampedro, J.J., Tauler, P., Ramis, J.M. i Monjo, M. (2025). Evaluation of Different Commercial Sealing Hemostatic Patches for Their Selection as Reservoirs for Localized Intraperitoneal Chemotherapy. ACS Pharmacology & Translational Science, 8(2), 499-509. https://doi.org/10.1021/acsptsci.4c00608 ca
dc.identifier.uri http://hdl.handle.net/11201/171315
dc.description.abstract [eng] Peritoneal carcinomatosis (PC) is typically treated by cytoreductive surgery (CRS) and subsequent hemotherapy. Sealing hemostatic patches (HP) are often used during these surgeries to prevent complications such as uncontrolled bleeding. These HP are made of biomaterials like oxidized cellulose or collagen with a binding agent, and beyond their usual function, they could also be used as drug delivery systems (DDS) for localized intraperitoneal chemotherapy in the tissue attached. Our first aim was to characterize and compare three different commercial HP (TachoSil®, Hemopatch®, and VerisetTM). Hemopatch® emerged as the most suitable candidate due to its combination of properties, including slow degradation, high hydrophilicity, excellent biological fluid absorption capacity, and moderate adhesive capacity alongside hemostasis. Utilizing Hemopatch® as a scaffold, we developed a new device incorporating a hyaluronic acid hydrogel loaded with cisplatin or olaparib. This approach facilitated sustained drug release for over 6 days, maintaining the anticancer efficacy of these agents on OVCAR-3 cells. In conclusion, integrating a DDS into HP shows potential for precisely delivering chemotherapeutic agents to any residual microscopic disease in PC following CRS. en
dc.format application/pdf en
dc.format.extent 499-509
dc.publisher ACS en
dc.relation.ispartof ACS Pharmacology & Translational Science, 2025, vol. 8, num.2, p. 499-509
dc.rights Attribution 4.0 International
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.subject.classification 54 - Química ca
dc.subject.classification 61 - Medicina ca
dc.subject.other 54 - Chemistry. Crystallography. Mineralogy en
dc.subject.other 61 - Medical sciences en
dc.title Evaluation of Different Commercial Sealing Hemostatic Patches for Their Selection as Reservoirs for Localized Intraperitoneal Chemotherapy en
dc.type info:eu-repo/semantics/article
dc.type info:eu-repo/semantics/publishedVersion
dc.type Article
dc.date.updated 2025-09-17T09:46:24Z
dc.rights.accessRights info:eu-repo/semantics/openAccess
dc.identifier.doi https://doi.org/10.1021/acsptsci.4c00608


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