Anna S Karyagina, Alexander V Grishin, Alina G Kudinova, Inna N Bulygina, Elizaveta V Koudan, Polina A Orlova, Vera P Datsenko, Anna V Zhulina, Tatyana M Grunina, Maria S Poponova, Mikhail S Krivozubov, Maria S Gromova, Natalia V Strukova, Maria S Generalova, Kirill E Nikitin, Igor V Shchetinin, Lev O Luchnikov, Svetlana V Zaitseva, Maria A Kirsanova, Eugene S Statnik, Fedor S Senatov, Vladimir G Lunin, Alexander V Gromov
{"title":"基于含有地奥赛德、BMP-2 和溶血素的结冷黄原水凝胶的双功能植入体,用于骨缺损修复和葡萄球菌感染控制。","authors":"Anna S Karyagina, Alexander V Grishin, Alina G Kudinova, Inna N Bulygina, Elizaveta V Koudan, Polina A Orlova, Vera P Datsenko, Anna V Zhulina, Tatyana M Grunina, Maria S Poponova, Mikhail S Krivozubov, Maria S Gromova, Natalia V Strukova, Maria S Generalova, Kirill E Nikitin, Igor V Shchetinin, Lev O Luchnikov, Svetlana V Zaitseva, Maria A Kirsanova, Eugene S Statnik, Fedor S Senatov, Vladimir G Lunin, Alexander V Gromov","doi":"10.1002/mabi.202400205","DOIUrl":null,"url":null,"abstract":"<p><p>A new dual-functional implant based on gellan-xanthan hydrogel with calcium-magnesium silicate ceramic diopside and recombinant lysostaphin and bone morphogenetic protein 2 (BMP-2)-ray is developed. In this composite, BMP-2 is immobilized on microparticles of diopside while lysostaphin is mixed directly into the hydrogel, providing sustained release of BMP-2 to allow gradual bone formation and rapid release of lysostaphin to eliminate infection immediately after implantation. Introduction of diopside of up to 3% (w/v) has a negligible effect on the mechanical properties of the hydrogel but provides a high sorption capacity for BMP-2. The hydrogels show good biocompatibility and antibacterial activity. Lysostaphin released from the implants over a 3 h period efficiently kills planktonic cells and completely destroys 24 h pre-formed biofilms of Staphylococcus aureus. Furthermore, in vivo experiments in a mouse model of critically-sized cranial defects infected with S. aureus show a complete lack of osteogenesis when implants contain only BMP-2, whereas, in the presence of lysostaphin, complete closure of the defect with newly formed mineralized bone tissue is observed. Thus, the new implantable gellan-xanthan hydrogel with diopside and recombinant lysostaphin and BMP-2 shows both osteogenic and antibacterial properties and represents a promising material for the treatment and/or prevention of osteomyelitis after bone trauma.</p>","PeriodicalId":18103,"journal":{"name":"Macromolecular bioscience","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2024-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dual-Functional Implant Based on Gellan-Xanthan Hydrogel with Diopside, BMP-2 and Lysostaphin for Bone Defect Repair and Control of Staphylococcal Infection.\",\"authors\":\"Anna S Karyagina, Alexander V Grishin, Alina G Kudinova, Inna N Bulygina, Elizaveta V Koudan, Polina A Orlova, Vera P Datsenko, Anna V Zhulina, Tatyana M Grunina, Maria S Poponova, Mikhail S Krivozubov, Maria S Gromova, Natalia V Strukova, Maria S Generalova, Kirill E Nikitin, Igor V Shchetinin, Lev O Luchnikov, Svetlana V Zaitseva, Maria A Kirsanova, Eugene S Statnik, Fedor S Senatov, Vladimir G Lunin, Alexander V Gromov\",\"doi\":\"10.1002/mabi.202400205\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A new dual-functional implant based on gellan-xanthan hydrogel with calcium-magnesium silicate ceramic diopside and recombinant lysostaphin and bone morphogenetic protein 2 (BMP-2)-ray is developed. In this composite, BMP-2 is immobilized on microparticles of diopside while lysostaphin is mixed directly into the hydrogel, providing sustained release of BMP-2 to allow gradual bone formation and rapid release of lysostaphin to eliminate infection immediately after implantation. Introduction of diopside of up to 3% (w/v) has a negligible effect on the mechanical properties of the hydrogel but provides a high sorption capacity for BMP-2. The hydrogels show good biocompatibility and antibacterial activity. Lysostaphin released from the implants over a 3 h period efficiently kills planktonic cells and completely destroys 24 h pre-formed biofilms of Staphylococcus aureus. Furthermore, in vivo experiments in a mouse model of critically-sized cranial defects infected with S. aureus show a complete lack of osteogenesis when implants contain only BMP-2, whereas, in the presence of lysostaphin, complete closure of the defect with newly formed mineralized bone tissue is observed. 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Dual-Functional Implant Based on Gellan-Xanthan Hydrogel with Diopside, BMP-2 and Lysostaphin for Bone Defect Repair and Control of Staphylococcal Infection.
A new dual-functional implant based on gellan-xanthan hydrogel with calcium-magnesium silicate ceramic diopside and recombinant lysostaphin and bone morphogenetic protein 2 (BMP-2)-ray is developed. In this composite, BMP-2 is immobilized on microparticles of diopside while lysostaphin is mixed directly into the hydrogel, providing sustained release of BMP-2 to allow gradual bone formation and rapid release of lysostaphin to eliminate infection immediately after implantation. Introduction of diopside of up to 3% (w/v) has a negligible effect on the mechanical properties of the hydrogel but provides a high sorption capacity for BMP-2. The hydrogels show good biocompatibility and antibacterial activity. Lysostaphin released from the implants over a 3 h period efficiently kills planktonic cells and completely destroys 24 h pre-formed biofilms of Staphylococcus aureus. Furthermore, in vivo experiments in a mouse model of critically-sized cranial defects infected with S. aureus show a complete lack of osteogenesis when implants contain only BMP-2, whereas, in the presence of lysostaphin, complete closure of the defect with newly formed mineralized bone tissue is observed. Thus, the new implantable gellan-xanthan hydrogel with diopside and recombinant lysostaphin and BMP-2 shows both osteogenic and antibacterial properties and represents a promising material for the treatment and/or prevention of osteomyelitis after bone trauma.
期刊介绍:
Macromolecular Bioscience is a leading journal at the intersection of polymer and materials sciences with life science and medicine. With an Impact Factor of 2.895 (2018 Journal Impact Factor, Journal Citation Reports (Clarivate Analytics, 2019)), it is currently ranked among the top biomaterials and polymer journals.
Macromolecular Bioscience offers an attractive mixture of high-quality Reviews, Feature Articles, Communications, and Full Papers.
With average reviewing times below 30 days, publication times of 2.5 months and listing in all major indices, including Medline, Macromolecular Bioscience is the journal of choice for your best contributions at the intersection of polymer and life sciences.