Ferrucci J T
Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston 02114.
Keio J Med. 1991 Dec;40(4):206-14. doi: 10.2302/kjm.40.206.
Superparamagnetic iron oxide (SPIO) particles are a potent new class of MR contrast agents affording improved detection of hepatic and splenic neoplasms. In this report we review the development of this agent through preclinical studies and early clinical results at Massachusetts General Hospital during a 5 year investigation. SPIO particles are sequestered by normal reticuloendothelial system (RES) phagocytic Kupffer cells but are not retained in tumor tissue. Consequently, there is a five fold increase in T2 relaxation between normal RES tissue and tumor with a comparable advantage in quantitative signal to noise ratio, contrast to noise ratio and lesion detectibility in the liver and spleen at MR imaging. Increased lesion conspicuity can be exploited to decrease threshold size for lesion detection to less than 3 mm. Clinically beneficial effects occur with a variety of mildly T2-weighted spin-echo pulse sequences; gradient-echo techniques show even greater benefit after administration of SPIO. Metabolically, pharmaceutical grade preparations are biodegradable and bioavailable, being rapidly turned over into body iron stores and incorporated into erythrocyte hemoglobin. Early dose escalation clinical trials have identified a probable clinical dose range of 10-20 mumol Fe/kg body weight. SPIO compounds evaluated to date are still investigational in the United States. Newer commercial formulations currently being evaluated may extend clinical safety margins.
超顺磁性氧化铁(SPIO)颗粒是一类新型高效的磁共振成像(MR)对比剂,可提高肝脏和脾脏肿瘤的检出率。在本报告中,我们回顾了在一项为期5年的研究中,该对比剂在麻省总医院的临床前研究及早期临床研究结果。SPIO颗粒可被正常网状内皮系统(RES)的吞噬性枯否细胞摄取,但不会在肿瘤组织中滞留。因此,正常RES组织与肿瘤组织之间的T2弛豫时间增加了5倍,在肝脏和脾脏的磁共振成像中,定量信噪比、对比噪声比及病灶可检测性方面具有类似优势。病灶清晰度的提高可用于将病灶检测的阈值大小降低至3毫米以下。使用多种轻度T2加权自旋回波脉冲序列可产生临床有益效果;注射SPIO后,梯度回波技术显示出更大优势。在代谢方面,药用级制剂具有生物可降解性和生物利用度,可迅速转化为体内铁储备并整合到红细胞血红蛋白中。早期剂量递增临床试验已确定临床可能的剂量范围为10-20微摩尔铁/千克体重。迄今为止,在美国,已评估的SPIO化合物仍处于研究阶段。目前正在评估的新型商业制剂可能会扩大临床安全范围。