In vitro and in vivo evaluation of biohybrid tissue-engineered vascular grafts with transformative 1H/19F MRI traceable scaffolds

IF 12.8 1区 医学 Q1 ENGINEERING, BIOMEDICAL Biomaterials Pub Date : 2024-06-17 DOI:10.1016/j.biomaterials.2024.122669
Elena Rama , Saurav Ranjan Mohapatra , Yukiharu Sugimura , Tomoyuki Suzuki , Stefan Siebert , Roman Barmin , Juliane Hermann , Jasmin Baier , Anne Rix , Teresa Lemainque , Susanne Koletnik , Asmaa Said Elshafei , Roger Molto Pallares , Seyed Mohammadali Dadfar , René H. Tolba , Volkmar Schulz , Joachim Jankowski , Christian Apel , Payam Akhyari , Stefan Jockenhoevel , Fabian Kiessling
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Abstract

Biohybrid tissue-engineered vascular grafts (TEVGs) promise long-term durability due to their ability to adapt to hosts' needs. However, the latter calls for sensitive non-invasive imaging approaches to longitudinally monitor their functionality, integrity, and positioning. Here, we present an imaging approach comprising the labeling of non-degradable and degradable TEVGs' components for their in vitro and in vivo monitoring by hybrid 1H/19F MRI. TEVGs (inner diameter 1.5 mm) consisted of biodegradable poly(lactic-co-glycolic acid) (PLGA) fibers passively incorporating superparamagnetic iron oxide nanoparticles (SPIONs), non-degradable polyvinylidene fluoride scaffolds labeled with highly fluorinated thermoplastic polyurethane (19F-TPU) fibers, a smooth muscle cells containing fibrin blend, and endothelial cells. 1H/19F MRI of TEVGs in bioreactors, and after subcutaneous and infrarenal implantation in rats, revealed that PLGA degradation could be faithfully monitored by the decreasing SPIONs signal. The 19F signal of 19F-TPU remained constant over weeks. PLGA degradation was compensated by cells’ collagen and α-smooth-muscle-actin deposition. Interestingly, only TEVGs implanted on the abdominal aorta contained elastin. XTT and histology proved that our imaging markers did not influence extracellular matrix deposition and host immune reaction. This concept of non-invasive longitudinal assessment of cardiovascular implants using 1H/19F MRI might be applicable to various biohybrid tissue-engineered implants, facilitating their clinical translation.

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采用可追踪 1H/19F 磁共振成像的生物杂交组织工程血管移植物的体外和体内评估
生物杂交组织工程血管移植物(TEVGs)能够适应宿主的需求,因此具有长期耐久性。然而,后者需要灵敏的非侵入性成像方法来纵向监测其功能、完整性和定位。在此,我们介绍一种成像方法,包括标记不可降解和可降解 TEVGs 的成分,以便通过 1H/19F 混合磁共振成像技术对其进行体外和体内监测。TEVG(内径 1.5 毫米)由可生物降解的聚乳酸-共聚乙醇酸(PLGA)纤维、被动结合超顺磁性氧化铁纳米粒子(SPIONs)的不可降解的聚偏氟乙烯支架、标记有高氟热塑性聚氨酯(19F-TPU)纤维的平滑肌细胞和内皮细胞组成。对生物反应器中的 TEVGs 以及大鼠皮下和肾下植入 TEVGs 后进行的 1H/19F 磁共振成像显示,PLGA 降解可通过 SPIONs 信号的下降得到忠实监测。19F-TPU 的 19F 信号在数周内保持不变。细胞的胶原蛋白和α-平滑肌肌动蛋白沉积补偿了PLGA降解。有趣的是,只有植入腹主动脉的 TEVGs 才含有弹性蛋白。XTT 和组织学证明,我们的成像标记物不会影响细胞外基质沉积和宿主免疫反应。这种利用 1H/19F 磁共振成像对心血管植入物进行无创纵向评估的概念可能适用于各种生物杂交组织工程植入物,从而促进其临床转化。
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来源期刊
Biomaterials
Biomaterials 工程技术-材料科学:生物材料
CiteScore
26.00
自引率
2.90%
发文量
565
审稿时长
46 days
期刊介绍: Biomaterials is an international journal covering the science and clinical application of biomaterials. A biomaterial is now defined as a substance that has been engineered to take a form which, alone or as part of a complex system, is used to direct, by control of interactions with components of living systems, the course of any therapeutic or diagnostic procedure. It is the aim of the journal to provide a peer-reviewed forum for the publication of original papers and authoritative review and opinion papers dealing with the most important issues facing the use of biomaterials in clinical practice. The scope of the journal covers the wide range of physical, biological and chemical sciences that underpin the design of biomaterials and the clinical disciplines in which they are used. These sciences include polymer synthesis and characterization, drug and gene vector design, the biology of the host response, immunology and toxicology and self assembly at the nanoscale. Clinical applications include the therapies of medical technology and regenerative medicine in all clinical disciplines, and diagnostic systems that reply on innovative contrast and sensing agents. The journal is relevant to areas such as cancer diagnosis and therapy, implantable devices, drug delivery systems, gene vectors, bionanotechnology and tissue engineering.
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