A rapid method for the preparation of an in vitro osteoporosis model of calf vertebrae: histological and biomechanical study.

IF 4.8 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Frontiers in Bioengineering and Biotechnology Pub Date : 2025-02-05 eCollection Date: 2025-01-01 DOI:10.3389/fbioe.2025.1527800
Anli Shi, Yijie Liu, Qiang Ma, Jiaxin Li, Jiawang Fan, Zhaohui Ge
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Abstract

Background: In vitro biomechanical testing is crucial for the preclinical assessment of novel implant designs. Given the constraints of limited supply and high costs associated with human specimens, calf spines are frequently employed as surrogates for human spines in both in vivo and in vitro biomechanical studies.

Methods: This study selected 60 spinal vertebrae from calves aged between 12 and 18 weeks. The specimens were randomly assigned to two treatment groups, A and B, each comprising 30 specimens. Group A served as the control without decalcification, while Group B underwent decalcification using an 18.3% ethylene diamine tetraacetic acid solution. The impact of decalcification was assessed through histological, imaging, and biomechanical analyses.

Findings: Decalcification took approximately 2 months, resulting in osteoporotic vertebrae with a bone mineral density reduction of approximately 50.89% compared to pre-decalcification levels. The bone microstructure was significantly altered, characterized by a decrease in trabecular thickness and number and an increase in trabecular separation. Additionally, the trabecular bone pattern factor (TBPf) and Structure Model Index (SMI) increased. The modulus of elasticity, yield stress, and ultimate stress of the vertebral bodies were all reduced in correlation with the decrease in bone mineral density, demonstrating a strong correlation between these parameters.

Interpretation: The data from this study indicate that the decalcification method is effective and capable of rapidly establishing an osteoporotic model suitable for biomechanical testing of clinical devices. This method offers the benefits of ease of operation, reliability, and a controllable degree of osteoporosis.

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一种快速制备小牛椎体体外骨质疏松模型的方法:组织学和生物力学研究。
背景:体外生物力学测试对于新型种植体设计的临床前评估至关重要。由于有限的供应和与人类标本相关的高成本的限制,在体内和体外生物力学研究中,小牛脊柱经常被用作人类脊柱的替代品。方法:选取12 ~ 18周龄犊牛60块脊椎骨。将标本随机分为A、B两组,每组30只。A组不脱钙,B组用18.3%乙二胺四乙酸溶液脱钙。通过组织学、影像学和生物力学分析评估脱钙的影响。结果:脱钙大约需要2个月,导致骨质疏松,骨密度比脱钙前降低约50.89%。骨微观结构明显改变,表现为骨小梁厚度和数量减少,骨小梁分离增加。骨小梁骨模式因子(TBPf)和结构模型指数(SMI)升高。椎体的弹性模量、屈服应力和极限应力均随骨密度的降低而降低,表明这些参数之间存在很强的相关性。解释:本研究数据表明脱钙方法是有效的,能够快速建立适合临床器械生物力学试验的骨质疏松模型。该方法具有操作简便、可靠性好、骨质疏松程度可控等优点。
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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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