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基于同步辐射传播的螺旋采集模式计算机断层成像术对低密度组织支架的成像。

Low-density tissue scaffold imaging by synchrotron radiation propagation-based imaging computed tomography with helical acquisition mode.

机构信息

Division of Biomedical Engineering, College of Engineering, University of Saskatchewan, Saskatoon, SK S7N 5A9, Canada.

Department of Anatomy, Physiology and Pharmacology, College of Medicine, University of Saskatchewan, Saskatoon, SK S7N 5A9, Canada.

出版信息

J Synchrotron Radiat. 2023 Mar 1;30(Pt 2):417-429. doi: 10.1107/S1600577523000772. Epub 2023 Feb 16.

DOI:10.1107/S1600577523000772
PMID:36891855
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10000810/
Abstract

Visualization of low-density tissue scaffolds made from hydrogels is important yet challenging in tissue engineering and regenerative medicine (TERM). For this, synchrotron radiation propagation-based imaging computed tomography (SR-PBI-CT) has great potential, but is limited due to the ring artifacts commonly observed in SR-PBI-CT images. To address this issue, this study focuses on the integration of SR-PBI-CT and helical acquisition mode (i.e. SR-PBI-HCT) to visualize hydrogel scaffolds. The influence of key imaging parameters on the image quality of hydrogel scaffolds was investigated, including the helical pitch (p), photon energy (E) and the number of acquisition projections per rotation/revolution (N), and, on this basis, those parameters were optimized to improve image quality and to reduce noise level and artifacts. The results illustrate that SR-PBI-HCT imaging shows impressive advantages in avoiding ring artifacts with p = 1.5, E = 30 keV and N = 500 for the visualization of hydrogel scaffolds in vitro. Furthermore, the results also demonstrate that hydrogel scaffolds can be visualized using SR-PBI-HCT with good contrast while at a low radiation dose, i.e. 342 mGy (voxel size of 26 µm, suitable for in vivo imaging). This paper presents a systematic study on hydrogel scaffold imaging using SR-PBI-HCT and the results reveal that SR-PBI-HCT is a powerful tool for visualizing and characterizing low-density scaffolds with a high image quality in vitro. This work represents a significant advance toward the non-invasive in vivo visualization and characterization of hydrogel scaffolds at a suitable radiation dose.

摘要

水凝胶基低密度组织支架的可视化在组织工程和再生医学(TERM)中非常重要,但具有挑战性。为此,同步辐射传播成像计算机断层扫描(SR-PBI-CT)具有很大的潜力,但由于在 SR-PBI-CT 图像中常见的环形伪影而受到限制。为了解决这个问题,本研究侧重于将 SR-PBI-CT 和螺旋采集模式(即 SR-PBI-HCT)集成到水凝胶支架的可视化中。研究了关键成像参数对水凝胶支架图像质量的影响,包括螺旋桨(p)、光子能量(E)和每旋转/旋转的采集投影数(N),在此基础上,对这些参数进行了优化,以提高图像质量,降低噪声水平和伪影。结果表明,SR-PBI-HCT 成像在避免环伪影方面具有显著优势,对于体外水凝胶支架的可视化,p = 1.5、E = 30keV 和 N = 500。此外,结果还表明,水凝胶支架可以使用 SR-PBI-HCT 进行可视化,具有良好的对比度,同时辐射剂量低,即 342mGy(体素大小为 26μm,适用于体内成像)。本文对使用 SR-PBI-HCT 进行水凝胶支架成像进行了系统研究,结果表明,SR-PBI-HCT 是一种强大的工具,可用于体外可视化和表征具有高质量图像的低密度支架。这项工作朝着在合适的辐射剂量下进行水凝胶支架的非侵入性体内可视化和表征迈出了重要一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/a7ae424457db/s-30-00417-fig11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/28d1b9ba3c77/s-30-00417-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/5e577bca9409/s-30-00417-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/392d2a1133f6/s-30-00417-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/4ba506725ece/s-30-00417-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/8a60a9c6096c/s-30-00417-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/595837f8e193/s-30-00417-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/5ff779ad63ad/s-30-00417-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/303f0972c340/s-30-00417-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/b8f4547bb19c/s-30-00417-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/5e465ccfd53b/s-30-00417-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/a7ae424457db/s-30-00417-fig11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/28d1b9ba3c77/s-30-00417-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/5e577bca9409/s-30-00417-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/392d2a1133f6/s-30-00417-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/4ba506725ece/s-30-00417-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/8a60a9c6096c/s-30-00417-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/595837f8e193/s-30-00417-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/5ff779ad63ad/s-30-00417-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/303f0972c340/s-30-00417-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/b8f4547bb19c/s-30-00417-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/5e465ccfd53b/s-30-00417-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b737/10000810/a7ae424457db/s-30-00417-fig11.jpg

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