Abstract

We present a fractional-order extension of the Bloch equations to describe anomalous NMR relaxation phenomena ( T 1 and T 2). The model has solutions in the form of Mittag–Leffler and stretched exponential functions that generalize conventional exponential relaxation. Such functions have been shown by others to be useful for describing dielectric and viscoelastic relaxation in complex, heterogeneous materials. Here, we apply these fractional-order T 1 and T 2 relaxation models to experiments performed at 9.4 and 11.7 Tesla on type I collagen gels, chondroitin sulfate mixtures, and to bovine nasal cartilage (BNC), a largely isotropic and homogeneous form of cartilage. The results show that the fractional-order analysis captures important features of NMR relaxation that are typically described by multi-exponential decay models. We find that the T 2 relaxation of BNC can be described in a unique way by a single fractional-order parameter ( α), in contrast to the lack of uniqueness of multi-exponential fits in the realistic setting of a finite signal-to-noise ratio. No anomalous behavior of T 1 was observed in BNC. In the single-component gels, for T 2 measurements, increasing the concentration of the largest components of cartilage matrix, collagen and chondroitin sulfate, results in a decrease in α, reflecting a more restricted aqueous environment. The quality of the curve fits obtained using Mittag–Leffler and stretched exponential functions are in some cases superior to those obtained using mono- and bi-exponential models. In both gels and BNC, α appears to account for micro-structural complexity in the setting of an altered distribution of relaxation times. This work suggests the utility of fractional-order models to describe T 2 NMR relaxation processes in biological tissues.

Highlights

  • Experimental NMR and clinical MRI rely on accurate mathematical models for longitudinal and transverse spin relaxation [1, 2]

  • These models are usually described by exponential functions [3, 4], it has long been recognized [5, 6] that mono-exponential functions or sums of exponentials may not adequately describe NMR relaxation in complex, heterogeneous, and anisotropic materials, such as biological tissue

  • Non-exponential, time-domain data obtained from MRS and MRI suggests the need for an alternative mathematical model to describe the relationship between relaxation processes and internal material structure

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Summary

Introduction

Experimental NMR and clinical MRI rely on accurate mathematical models for longitudinal and transverse spin relaxation [1, 2] These models are usually described by exponential functions [3, 4], it has long been recognized [5, 6] that mono-exponential functions or sums of exponentials may not adequately describe NMR relaxation in complex, heterogeneous, and anisotropic materials, such as biological tissue. Non-exponential, time-domain data obtained from MRS and MRI suggests the need for an alternative mathematical model to describe the relationship between relaxation processes and internal material structure. Such structures in biological tissues restrict the movement of water on multiple time and length scales, ranging from nanoseconds for the rotational correlation time to hundreds of milliseconds for T1 relaxation. It is reasonable to consider such models in the analysis and interpretation of NMR relaxation in biological tissues

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