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控制聚甲基丙烯酸甲酯骨水泥中的抗生素释放。

Controlling Antibiotic Release from Polymethylmethacrylate Bone Cement.

作者信息

Wall Victoria, Nguyen Thi-Hiep, Nguyen Nghi, Tran Phong A

机构信息

Faculty of Medicine (Princess Alexandra Hospital), St Lucia Campus, The University of Queensland, Brisbane, QLD 4072, Australia.

Interface Science and Materials Engineering Group, School of Mechanical, Medical and Process Engineering, Queensland University of Technology (QUT), 2 George Street, Brisbane, QLD 4000, Australia.

出版信息

Biomedicines. 2021 Jan 1;9(1):26. doi: 10.3390/biomedicines9010026.

Abstract

Bone cement is used as a mortar for securing bone implants, as bone void fillers or as spacers in orthopaedic surgery. Antibiotic-loaded bone cements (ALBCs) have been used to prevent and treat prosthetic joint infections by providing a high antibiotic concentration around the implanted prosthesis. High antibiotic concentrations are, on the other hand, often associated with tissue toxicity. Controlling antibiotic release from ALBCS is key to achieving effective infection control and promoting prosthesis integration with the surrounding bone tissue. However, current ALBCs still need significant improvement in regulating antibiotic release. In this review, we first provide a brief introduction to prosthetic joint infections, and the background concepts of therapeutic efficacy and toxicity in antibiotics. We then review the current state of ALBCs and their release characteristics before focusing on the research and development in controlling the antibiotic release and osteo-conductivity/inductivity. We then conclude by a discussion on the need for better in vitro experiment designs such that the release results can be extrapolated to predict better the local antibiotic concentrations in vivo.

摘要

骨水泥在骨科手术中用作固定骨植入物的灰浆、骨缺损填充剂或间隔物。载抗生素骨水泥(ALBCs)通过在植入的假体周围提供高抗生素浓度来预防和治疗人工关节感染。另一方面,高抗生素浓度常常与组织毒性相关。控制ALBCs中抗生素的释放是实现有效感染控制以及促进假体与周围骨组织整合的关键。然而,目前的ALBCs在调节抗生素释放方面仍需显著改进。在这篇综述中,我们首先简要介绍人工关节感染以及抗生素治疗效果和毒性的背景概念。然后,在重点关注控制抗生素释放和骨传导性/诱导性的研发之前,我们回顾ALBCs的现状及其释放特性。最后,我们通过讨论更好的体外实验设计的必要性来得出结论,以便能够外推释放结果以更好地预测体内局部抗生素浓度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35db/7824110/d0b8a0efe76b/biomedicines-09-00026-g001.jpg

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