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Experimental Issues in the Measurement of Multi-component Relaxation Times in Articular Cartilage by Microscopic MRI

机译:显微MRI测量关节软骨多组分弛豫时间的实验问题

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摘要

A number of experimental issues in the measurement of multi-component T2 and T1ρ relaxations in native and enzymatically digested articular cartilage were investigated by microscopic MRI (μMRI). The issues included the bath solutions (physiological saline and phosphate buffered saline (PBS)), the imaging resolution (35 to 140 μm), the specimen orientations (0° and 55°), and the strength of spin-lock frequencies (0.5 to 2 kHz) in the T1ρ experiments. In addition to cartilage, the samples of agar gel and doped water solution were also used in the investigation. Two imaging sequences were used: CPMG-SE and MSME. All raw data were analyzed by the non-negative least square (NNLS) method. The MSME sequence was shown to result in the observation of multi-component T2, even in the gel and liquid samples, demonstrating the artificial uncleanness of this sequence in the multi-component measurements. The soaking of cartilage in PBS reduced the observable T2 components to one at both 0° and 55°, suggesting the effect of phosphate ions on proton exchange between different pools of water molecules. The cartilage orientation with respect to the external magnetic field and the spin-lock strengths in the T1ρ experiment both affected the quantification of the multi-component relaxation. The transitions between a mono-component and multi-components in cartilage under various experimental conditions call for the extra caution in interpreting the relaxation results.
机译:通过显微镜MRI(μMRI)研究了测量天然和酶消化的关节软骨中多组分T2和T1ρ弛豫的许多实验问题。问题包括浴液(生理盐水和磷酸盐缓冲盐水(PBS)),成像分辨率(35至140μm),样品方向(0°和55°)以及自旋锁定频率的强度(0.5至T1ρ实验中为2 kHz)。除软骨外,琼脂凝胶和掺杂的水溶液样品也用于研究。使用了两个成像序列:CPMG-SE和MSME。所有原始数据均通过非负最小二乘(NNLS)方法进行分析。 MSME序列显示出即使在凝胶和液体样品中也能观察到多组分T2,证明了在多组分测量中该序列的人为不洁。软骨在PBS中的浸泡将可观察到的T2组分在0°和55°处均降低为一个,表明磷酸根离子对不同水分子池之间质子交换的影响。 T1ρ实验中相对于外部磁场的软骨取向和自旋锁定强度都影响了多组分弛豫的定量。在各种实验条件下,软骨中单组分和多组分之间的过渡要求在解释松弛结果时格外小心。

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