抗菌3D打印植入物用于假体周围关节感染。

IF 5.5 3区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Iván Yuste, Francis C Luciano, Carmina Rodríguez, Bianca I Ramirez, Chrysi Rapti, Brayan J Anaya, Aikaterini Lalatsa, Almudena Ribed-Sánchez, Pablo Sanz-Ruiz, Elena González-Burgos, Dolores R Serrano
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引用次数: 0

摘要

假体周围关节感染(PJIs)仍然是髋关节和膝关节置换术后的一个严重并发症,影响了发达国家1-5%的患者,对患者、临床医生和医疗保健系统构成了重大挑战。传统的预防策略,如含抗生素的骨水泥,存在植入后药物释放有限和潜在的机械完整性损害的问题。为了克服这些限制,我们开发了一种个性化的3d打印植入物,旨在与关节假体的髋臼组件相结合。这些植入物可以提供单一治疗或两性霉素B (AmB)和万古霉素(VAN)的联合治疗,针对真菌和细菌病原体。该植入物采用生物相容性聚乙烯醇-聚乙二醇(PVA-PEG)基质,通过熔融沉积建模制成,可在60秒内实现被动药物装载和快速粘附到假体表面,最大限度地减少手术时间。体外试验证实对念珠菌(白色念珠菌、副枯枝念珠菌、光秃念珠菌、克鲁塞念珠菌)和葡萄球菌(金黄色葡萄球菌、表皮葡萄球菌)具有广谱抗菌活性。VAN释放迅速,而AmB则表现出长达10小时的持续释放,两者都保持48小时的饱和溶解度。值得注意的是,与游离药物相比,负载AmB的植入物的溶血毒性降低了5倍。这些结果突出了3d打印药物洗脱植入物作为预防和早期治疗PJIs的临床可行解决方案的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antimicrobial 3D printed implants for periprosthetic joint infections.

Periprosthetic joint infections (PJIs) remain a serious complication following hip and knee arthroplasty, affecting 1-5% of patients in developed countries and posing significant challenges to patients, clinicians, and healthcare systems. Conventional prophylactic strategies, such as antibiotic-loaded bone cement, suffer from limited post-implantation drug release and potential compromise of mechanical integrity. To overcome these limitations, we developed a personalized, 3D-printed implant designed to integrate with the acetabular component of joint prostheses. These implants deliver either monotherapy or a combination of amphotericin B (AmB) and vancomycin (VAN), targeting both fungal and bacterial pathogens. Fabricated via fused deposition modeling using a biocompatible polyvinyl alcohol-polyethylene glycol (PVA-PEG) matrix, the implants enable passive drug loading and rapid adhesion to prosthetic surfaces within 60 s, minimizing operative time. In vitro testing confirmed broad-spectrum antimicrobial activity against Candida spp. (C. albicans, C. parapsilosis, C. glabrata, C. krusei) and Staphylococcus spp. (S. aureus, S. epidermidis). VAN was released rapidly, while AmB exhibited sustained release for up to 10 h, with both maintaining saturation solubility for 48 h. Notably, AmB-loaded implants showed five-fold lower hemolytic toxicity compared to free drug. These results highlight the potential of 3D-printed, drug-eluting implants as a clinically viable solution for the prevention and early treatment of PJIs.

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来源期刊
Drug Delivery and Translational Research
Drug Delivery and Translational Research MEDICINE, RESEARCH & EXPERIMENTALPHARMACOL-PHARMACOLOGY & PHARMACY
CiteScore
11.70
自引率
1.90%
发文量
160
期刊介绍: The journal provides a unique forum for scientific publication of high-quality research that is exclusively focused on translational aspects of drug delivery. Rationally developed, effective delivery systems can potentially affect clinical outcome in different disease conditions. Research focused on the following areas of translational drug delivery research will be considered for publication in the journal. Designing and developing novel drug delivery systems, with a focus on their application to disease conditions; Preclinical and clinical data related to drug delivery systems; Drug distribution, pharmacokinetics, clearance, with drug delivery systems as compared to traditional dosing to demonstrate beneficial outcomes Short-term and long-term biocompatibility of drug delivery systems, host response; Biomaterials with growth factors for stem-cell differentiation in regenerative medicine and tissue engineering; Image-guided drug therapy, Nanomedicine; Devices for drug delivery and drug/device combination products. In addition to original full-length papers, communications, and reviews, the journal includes editorials, reports of future meetings, research highlights, and announcements pertaining to the activities of the Controlled Release Society.
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