Bendel P, Sauerwein W
Department of Chemical Services, MR Center, The Weizmann Institute of Science, Rehovot, Israel.
Med Phys. 2001 Feb;28(2):178-83. doi: 10.1118/1.1339227.
Boron Neutron Capture Therapy (BNCT), an experimental binary cancer treatment modality, requires selective targeting of 10B containing compounds to tumors. One of the compounds under evaluation in an EORTC phase I trial, and used in Japan for patient treatments for many years, is borocaptate sodium (BSH, also known as sulfhydril boron hydride). To optimize the clinical applications, a noninvasive method is needed to monitor the distribution of the boron compound, and NMR may offer such a possibility. A comparison between the relative sensitivities for detecting BSH by 10B or 1H NMR was conducted at two magnetic field strengths: 2 and 4.7 T. At each field strength, similar-sized radio frequency (rf) coils were used for both nuclei. Theoretical predictions for the intrinsic signal to noise (S/N) advantage of 1H over 10B detection vary between a factor of 5.4 and a factor of 28.9, depending on whether the effective resistance is dominated by coil losses or sample losses. Our tests, conducted on relatively small aqueous samples, which loaded the coils less than expected for animal or human subjects, resulted nevertheless in advantage factors close to the lower limit of this range. The measured S/N detection advantage factors for 1H were about 5.2 at 4.7 T, using a dedicated 1H coil, and 7.7 at 2 T, where the measurements were conducted with a double-tuned coil. However, when predicting the expected performance for in vivo MRS or MRI, one should bear in mind that proton detection has to be conducted by spectral-editing pulse sequences with an inherent S/N loss by at least a factor of 2, and that the T1 relaxation time for 10B in BSH is about 30 times shorter than the 1HT1 value. In view of these considerations, direct 10B detection could well be the preferred strategy for MRI/MRS of BSH in vivo.
硼中子俘获疗法(BNCT)是一种实验性的二元癌症治疗方式,需要将含硼-10的化合物选择性地靶向肿瘤。硼酸钠(BSH,也称为巯基硼氢化物)是正在欧洲癌症研究与治疗组织(EORTC)一期试验中评估且在日本已用于患者治疗多年的化合物之一。为了优化临床应用,需要一种非侵入性方法来监测硼化合物的分布,而核磁共振(NMR)可能提供这样一种可能性。在2 T和4.7 T这两种磁场强度下,对通过硼-10或氢-1 NMR检测硼酸钠的相对灵敏度进行了比较。在每个磁场强度下,两种原子核均使用尺寸相似的射频(rf)线圈。氢-1相对于硼-10检测的固有信噪比(S/N)优势的理论预测值在5.4倍至28.9倍之间变化,这取决于有效电阻是由线圈损耗还是样品损耗主导。我们在相对较小的水性样品上进行的测试,这些样品对线圈的负载低于动物或人体受试者的预期,但得到的优势因子仍接近该范围的下限。使用专用氢-1线圈时,在4.7 T下氢-1的测量信噪比优势因子约为5.2,在2 T下使用双调谐线圈进行测量时为7.7。然而,在预测体内磁共振波谱(MRS)或磁共振成像(MRI)的预期性能时,应记住质子检测必须通过频谱编辑脉冲序列进行,这会导致固有信噪比损失至少2倍,并且硼酸钠中硼-10的T1弛豫时间比氢-1的T1值短约30倍。鉴于这些考虑因素,直接检测硼-10很可能是体内硼酸钠MRI/MRS的首选策略。