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用于支架引导乳房重建的抗菌白蛋白 - 单宁酸涂层

Antibacterial Albumin-Tannic Acid Coatings for Scaffold-Guided Breast Reconstruction.

作者信息

Cometta Silvia, Bock Nathalie, Suresh Sinduja, Dargaville Tim R, Hutmacher Dietmar W

机构信息

Centre in Regenerative Medicine, Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, QLD, Australia.

School of Mechanical, Medical and Process Engineering, Science and Engineering Faculty, Queensland University of Technology, Brisbane, QLD, Australia.

出版信息

Front Bioeng Biotechnol. 2021 Mar 31;9:638577. doi: 10.3389/fbioe.2021.638577. eCollection 2021.

Abstract

Infection is the major cause of morbidity after breast implant surgery. Biodegradable medical-grade polycaprolactone (mPCL) scaffolds designed and rooted in evidence-based research offer a promising alternative to overcome the limitations of routinely used silicone implants for breast reconstruction. Nevertheless, as with any implant, biodegradable scaffolds are susceptible to bacterial infection too, especially as bacteria can rapidly colonize the biomaterial surface and form biofilms. Biofilm-related infections are notoriously challenging to treat and can lead to chronic infection and persisting inflammation of surrounding tissue. To date, no clinical solution that allows to efficiently prevent bacterial infection while promoting correct implant integration, has been developed. In this study, we demonstrated for the first time, to our knowledge that the physical immobilization of 1 and 5% human serum albumin (HSA) onto the surface of 3D printed macro- and microporous mPCL scaffolds, resulted in a reduction of colonization by 71.7 ± 13.6% and 54.3 ± 12.8%, respectively. Notably, when treatment of scaffolds with HSA was followed by tannic acid (TA) crosslinking/stabilization, uniform and stable coatings with improved antibacterial activity were obtained. The HSA/TA-coated scaffolds were shown to be stable when incubated at physiological conditions in cell culture media for 7 days. Moreover, they were capable of inhibiting the growth of and , two most commonly found bacteria in breast implant infections. Most importantly, 1%HSA/10%TA- and 5%HSA/1%TA-coated scaffolds were able to reduce colonization on the mPCL surface, by 99.8 ± 0.1% and 98.8 ± 0.6%, respectively, in comparison to the non-coated control specimens. This system offers a new biomaterial strategy to effectively translate the prevention of biofilm-related infections on implant surfaces without relying on the use of prophylactic antibiotic treatment.

摘要

感染是乳房植入手术后发病的主要原因。基于循证研究设计的可生物降解医用级聚己内酯(mPCL)支架,为克服常规用于乳房重建的硅胶植入物的局限性提供了一种有前景的替代方案。然而,与任何植入物一样,可生物降解支架也易受细菌感染,尤其是因为细菌可迅速在生物材料表面定植并形成生物膜。与生物膜相关的感染 notoriously challenging to treat,可导致慢性感染和周围组织的持续炎症。迄今为止,尚未开发出一种能够在促进植入物正确整合的同时有效预防细菌感染的临床解决方案。在本研究中,据我们所知,我们首次证明将1%和5%的人血清白蛋白(HSA)物理固定在3D打印的大孔和微孔mPCL支架表面,分别使定植减少了71.7±13.6%和54.3±12.8%。值得注意的是,当用HSA处理支架后进行单宁酸(TA)交联/稳定化处理时,可获得具有改善抗菌活性的均匀且稳定的涂层。HSA/TA涂层支架在细胞培养基中于生理条件下孵育7天时显示出稳定性。此外,它们能够抑制乳房植入物感染中最常见的两种细菌 和 的生长。最重要的是,与未涂层的对照标本相比,1%HSA/10%TA和5%HSA/1%TA涂层的支架能够分别将mPCL表面的 定植减少99.8±0.1%和98.8±0.6%。该系统提供了一种新的生物材料策略,可有效预防植入物表面与生物膜相关的感染,而无需依赖预防性抗生素治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2694/8044405/7a5aeb69f9db/fbioe-09-638577-g001.jpg

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