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分子印迹聚合物:塑造早期骨质流失检测的未来——综述

Molecularly Imprinted Polymers: Shaping the Future of Early-Stage Bone Loss Detection-A Review.

作者信息

Agnishwaran Bala, Manivasagam Geetha, Udduttula Anjaneyulu

机构信息

Centre for Biomaterials, Cellular and Molecular Theranostics (CBCMT), Vellore Institute of Technology (VIT), Vellore-632014, Tamil Nadu, India.

School of Bio Sciences and Technology (SBST), Vellore Institute of Technology (VIT), Vellore-632014, Tamil Nadu, India.

出版信息

ACS Omega. 2024 Feb 15;9(8):8730-8742. doi: 10.1021/acsomega.3c08977. eCollection 2024 Feb 27.

Abstract

Osteoporosis is the deterioration of bone mineral density (BMD) because of an imbalance between bone resorption and formation, which might happen due to lots of factors like age, hormonal imbalance, and several others. While this occurrence is prevalent in both genders, it is more common in women, especially postmenopausal women. It is an asymptomatic disease that is underlying until the first incidence of a fracture. The bone is weakened, making it more susceptible to fracture. Even a low trauma can result in a fracture, making osteoporosis an even more alarming disease. These fractures can sometimes be fatal or can make the patient bedridden. Osteoporosis is an understudied disease, and there are certain limitations in diagnosing and early-stage detection of this condition. The standard method of dual X-ray absorptiometry can be used to some extent and can be detected in standard radiographs after the deterioration of a significant amount of bone mass. Clinically assessing osteoporosis using biomarkers can still be challenging, as clinical tests can be expensive and cannot be accessed by most of the general population. In addition, manufacturing antibodies specific to these biomarkers can be a challenging, time-consuming, and expensive method. As an alternative to these antibodies, molecularly imprinted polymers (MIPs) can be used in the detection of these biomarkers. This Review provides a comprehensive exploration of bone formation, resorption, and remodeling processes, linking them to the pathophysiology of osteoporosis. It details biomarker-based detection and diagnosis methods, with a focus on MIPs for sensing CTX-1, NTX-1, and other biomarkers. The discussion compares traditional clinical practices with MIP-based sensors, revealing comparable sensitivity with identified limitations. Additionally, the Review contrasts antibody-functionalized sensors with MIPs. Finally, our Review concludes by highlighting the potential of MIPs in future early-stage osteoporosis detection.

摘要

骨质疏松症是由于骨吸收与形成之间的失衡导致骨矿物质密度(BMD)下降,这可能由多种因素引起,如年龄、激素失衡等。虽然这种情况在男女中都很普遍,但在女性中更为常见,尤其是绝经后女性。它是一种无症状疾病,在首次发生骨折之前一直潜伏。骨骼变得脆弱,更容易发生骨折。即使是低创伤也可能导致骨折,使骨质疏松症成为一种更令人担忧的疾病。这些骨折有时可能是致命的,或者会使患者卧床不起。骨质疏松症是一种研究不足的疾病,在诊断和早期检测方面存在一定局限性。双能X线吸收法的标准方法在一定程度上可以使用,并且在大量骨质流失后可以在标准X光片中检测到。使用生物标志物临床评估骨质疏松症仍然具有挑战性,因为临床检测可能昂贵,而且大多数普通人群无法进行。此外,制造针对这些生物标志物的特异性抗体可能是一种具有挑战性、耗时且昂贵的方法。作为这些抗体的替代物,分子印迹聚合物(MIPs)可用于检测这些生物标志物。本综述全面探讨了骨形成、吸收和重塑过程,并将它们与骨质疏松症的病理生理学联系起来。它详细介绍了基于生物标志物的检测和诊断方法,重点是用于检测CTX-1、NTX-1和其他生物标志物的MIPs。讨论将传统临床实践与基于MIP的传感器进行了比较,揭示了具有已确定局限性的可比灵敏度。此外,本综述还对比了抗体功能化传感器与MIPs。最后,我们的综述通过强调MIPs在未来早期骨质疏松症检测中的潜力得出结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d82b/10905706/8927a0d3645f/ao3c08977_0001.jpg

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