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具有载抗生素层状填料的3D增材制造复合支架用于预防骨感染和组织再生。

3D additive manufactured composite scaffolds with antibiotic-loaded lamellar fillers for bone infection prevention and tissue regeneration.

作者信息

Cámara-Torres María, Duarte Stacy, Sinha Ravi, Egizabal Ainhoa, Álvarez Noelia, Bastianini Maria, Sisani Michele, Scopece Paolo, Scatto Marco, Bonetto Alessandro, Marcomini Antonio, Sanchez Alberto, Patelli Alessandro, Mota Carlos, Moroni Lorenzo

机构信息

Maastricht University, MERLN Institute for Technology-Inspired Regenerative Medicine, Complex Tissue Regeneration Department, Universiteitssingel 40, 6229, ER, Maastricht, the Netherlands.

TECNALIA, Basque Research and Technology Alliance (BRTA), Mikeletegi Pasealekua 2, 20009, Donostia-San Sebastian, Spain.

出版信息

Bioact Mater. 2020 Oct 15;6(4):1073-1082. doi: 10.1016/j.bioactmat.2020.09.031. eCollection 2021 Apr.

Abstract

Bone infections following open bone fracture or implant surgery remain a challenge in the orthopedics field. In order to avoid high doses of systemic drug administration, optimized local antibiotic release from scaffolds is required. 3D additive manufactured (AM) scaffolds made with biodegradable polymers are ideal to support bone healing in non-union scenarios and can be given antimicrobial properties by the incorporation of antibiotics. In this study, ciprofloxacin and gentamicin intercalated in the interlamellar spaces of magnesium aluminum layered double hydroxides (MgAl) and α-zirconium phosphates (ZrP), respectively, are dispersed within a thermoplastic polymer by melt compounding and subsequently processed via high temperature melt extrusion AM (~190 °C) into 3D scaffolds. The inorganic fillers enable a sustained antibiotics release through the polymer matrix, controlled by antibiotics counterions exchange or pH conditions. Importantly, both antibiotics retain their functionality after the manufacturing process at high temperatures, as verified by their activity against both Gram + and Gram - bacterial strains. Moreover, scaffolds loaded with filler-antibiotic do not impair human mesenchymal stromal cells osteogenic differentiation, allowing matrix mineralization and the expression of relevant osteogenic markers. Overall, these results suggest the possibility of fabricating dual functionality 3D scaffolds via high temperature melt extrusion for bone regeneration and infection prevention.

摘要

开放性骨折或植入手术后的骨感染仍然是骨科领域的一项挑战。为了避免大剂量全身性给药,需要从支架中实现优化的局部抗生素释放。由可生物降解聚合物制成的3D增材制造(AM)支架是支持骨不连情况下骨愈合的理想选择,并且可以通过掺入抗生素赋予抗菌性能。在本研究中,分别插层于镁铝层状双氢氧化物(MgAl)和磷酸锆(ZrP)层间空间的环丙沙星和庆大霉素,通过熔融共混分散在热塑性聚合物中,随后通过高温熔融挤出增材制造(约190°C)加工成3D支架。无机填料通过聚合物基质实现抗生素的持续释放,这由抗生素抗衡离子交换或pH条件控制。重要的是,两种抗生素在高温制造过程后仍保留其功能,这通过它们对革兰氏阳性和革兰氏阴性菌株的活性得到验证。此外,负载填料 - 抗生素的支架不会损害人间充质基质细胞的成骨分化,允许基质矿化和相关成骨标志物的表达。总体而言,这些结果表明通过高温熔融挤出制造具有双重功能的3D支架用于骨再生和感染预防的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c852/7569267/fb15df75a488/fx1.jpg

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