Haoyun Su, Lok Hin Law, Yang Liu, Jianpan Huang, Kannie W Y Chan
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引用次数: 0
摘要
二甲基亚砜(DMSO)具有广泛的生物医学用途,如低温保护剂和疏水性药物载体。在这里,我们首次报告了二甲基亚砜能在-2 ppm左右产生独特的化学交换饱和转移(CEST)信号。二甲基亚砜的结构类似物,包括烷基和质基溶剂,也显示出 -1.4 至 -3.8 ppm 的 CEST 信号。当 CEST 检测巴比妥酸(BA)溶于二甲基亚砜溶液并共同负载到脂质体中时,在 5 和 -2 ppm 处观察到两个明显的峰,这表明二甲基亚砜及相关溶剂系统可通过 CEST 以无标记的方式进行监测,并可进一步应用于药物纳米载体的成像。参考之前的研究,可能存在分子相互作用或磁化传递途径,如中继核奥弗霍瑟增强(rNOE),从而导致在 Z 光谱的负偏移频率上出现这种可检测到的 CEST 对比。我们的研究结果表明,有机溶剂的小分子可能参与了与水的磁化传递过程,并很容易被 CEST 磁共振成像 (MRI) 检测到,这为检测溶剂-水和溶剂-药物相互作用提供了一条新途径。
CEST effect of dimethyl sulfoxide at negative offset frequency.
Dimethyl sulfoxide (DMSO) has wide biomedical applications such as cryoprotectant and hydrophobic drug carrier. Here, we report for the first time that DMSO can generate a distinctive chemical exchange saturation transfer (CEST) signal at around -2 ppm. Structural analogs of DMSO, including aprotic and protic solvents, also demonstrated CEST signals from -1.4 to -3.8 ppm. When CEST detectable barbituric acid (BA) was dissolved in DMSO solution and was co-loaded to liposome, two obvious peaks at 5 and -2 ppm were observed, indicating that DMSO and related solvent system can be monitored in a label-free manner via CEST, which can be further applied to imaging drug nanocarriers. With reference to previous studies, there could be molecular interactions or magnetization transfer pathways, such as the relayed nuclear Overhauser enhancement (rNOE), that lead to this detectable CEST contrast at negative offset frequencies of the Z-spectrum. Our findings suggest that small molecules of organic solvents could be involved in magnetization transfer processes with water and readily detected by CEST magnetic resonance imaging (MRI), providing a new avenue for detecting solvent-water and solvent-drug interactions.
期刊介绍:
NMR in Biomedicine is a journal devoted to the publication of original full-length papers, rapid communications and review articles describing the development of magnetic resonance spectroscopy or imaging methods or their use to investigate physiological, biochemical, biophysical or medical problems. Topics for submitted papers should be in one of the following general categories: (a) development of methods and instrumentation for MR of biological systems; (b) studies of normal or diseased organs, tissues or cells; (c) diagnosis or treatment of disease. Reports may cover work on patients or healthy human subjects, in vivo animal experiments, studies of isolated organs or cultured cells, analysis of tissue extracts, NMR theory, experimental techniques, or instrumentation.