Pickup Stephen, Wood Andrew K W, Kundel Harold L
Department of Radiology, University of Pennsylvania Medical Center, 3400 Spruce Street, Philadelphia, PA 19104, USA.
Magn Reson Med. 2005 Jan;53(1):35-40. doi: 10.1002/mrm.20336.
In vivo measurements of gadodiamide (Gd-DTPA-BMA) T(1) relaxivity were performed at 4.7 T in injured and normal rat brains. Cerebral lesions were induced in nine rats by a localized freezing method. T(1) maps of the lesions were generated before and after injection of Gd-DTPA-BMA (0.1-0.6 mmol/kg). Samples of normal and necrotic brain were collected postmortem; the wet and dry weights were determined, and Gd content was measured by inductively coupled plasma mass spectroscopy. The in vivo relaxivity was determined by a linear fit of a plot of the change in relaxation rate following injection of the contrast agent as a function of Gd content. This analysis yielded a relaxivity in the injured brain of 2.8 sec(-1) mmol(-1) kg tissue water at 36 degrees C. The water weight fraction was 0.90 +/- SD 0.02 wt/wt in injured brain and 0.79 +/- 0.02 in normal brain. Relaxivity measurements were also performed on solutions of Gd-DTPA-BMA (0.0-0.6 mmol) and albumin (0-30% wt/wt) in normal saline at room and physiologic temperatures. The relaxivity in the albumin/saline increased with increasing solids content with values of 4.0-4.9 sec(-1) mmol(-1)kg at 21 degrees C and 3.4-4.5 sec(-1) mmol(-1) kg at 37 degrees C. The relaxivity of the tissues differed significantly from that of the saline solutions of comparable solids content, suggesting that the solids content of a tissue is not the only factor that determines in vivo relaxivity.
在4.7T磁场下对受伤和正常大鼠脑内的钆双胺(Gd-DTPA-BMA)T(1)弛豫率进行了体内测量。通过局部冷冻法在9只大鼠中诱导脑损伤。在注射Gd-DTPA-BMA(0.1 - 0.6 mmol/kg)之前和之后生成损伤部位的T(1)图谱。在死后收集正常和坏死脑组织样本;测定湿重和干重,并通过电感耦合等离子体质谱法测量钆含量。通过将注射造影剂后弛豫率变化的曲线作为钆含量的函数进行线性拟合来确定体内弛豫率。该分析得出在36℃时受伤脑内的弛豫率为2.8秒^(-1)毫摩尔^(-1)千克组织水。受伤脑内水的重量分数为0.90±标准差0.02重量/重量,正常脑内为0.79±0.02。还在室温和生理温度下对Gd-DTPA-BMA(0.0 - 0.6 mmol)和白蛋白(0 - 30%重量/重量)在生理盐水中的溶液进行了弛豫率测量。白蛋白/生理盐水溶液中的弛豫率随固体含量增加而增加,在21℃时为4.0 - 4.9秒^(-1)毫摩尔^(-1)千克,在37℃时为3.4 - 4.5秒^(-1)毫摩尔^(-1)千克。组织的弛豫率与具有可比固体含量的生理盐水溶液的弛豫率有显著差异,这表明组织的固体含量不是决定体内弛豫率的唯一因素。