Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
PLoS One. 2013 Aug 15;8(8):e71274. doi: 10.1371/journal.pone.0071274. eCollection 2013.
In vivo real time spectroscopic imaging of hyperpolarized ¹³C labeled metabolites shows substantial promise for the assessment of physiological processes that were previously inaccessible. However, reliable and reproducible methods of measurement are necessary to maximize the effectiveness of imaging biomarkers that may one day guide personalized care for diseases such as cancer. Animal models of human disease serve as poor reference standards due to the complexity, heterogeneity, and transient nature of advancing disease. In this study, we describe the reproducible conversion of hyperpolarized [1-¹³C]-pyruvate to [1-¹³C]-lactate using a novel synthetic enzyme phantom system. The rate of reaction can be controlled and tuned to mimic normal or pathologic conditions of varying degree. Variations observed in the use of this phantom compare favorably against within-group variations observed in recent animal studies. This novel phantom system provides crucial capabilities as a reference standard for the optimization, comparison, and certification of quantitative imaging strategies for hyperpolarized tracers.
对 ¹³C 标记代谢物进行的体内实时光谱成像是评估以前无法达到的生理过程的重要手段。然而,为了使成像生物标志物的有效性最大化,这些标志物将来可能会指导癌症等疾病的个性化治疗,就需要可靠且可重复的测量方法。由于疾病进展的复杂性、异质性和短暂性,人类疾病的动物模型不能作为可靠的参考标准。在这项研究中,我们描述了使用新型合成酶虚拟模型系统,可重复地将 ¹³C 标记的丙酮酸转化为 ¹³C 标记的乳酸。可以控制和调整反应速率,以模拟不同程度的正常或病理条件。与最近的动物研究中观察到的组内变化相比,使用这种虚拟模型观察到的变化具有优势。这种新型虚拟模型系统为优化、比较和认证用于极化示踪剂的定量成像策略提供了重要的参考标准。