Hines J V, Ammar G M, Buss J, Schmalbrock P
Division of Medicinal Chemistry & Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210,
Bioconjug Chem. 1999 Mar-Apr;10(2):155-8. doi: 10.1021/bc980103v.
An antisense paramagnetic oligonucleotide analogue targeted to a model macromolecular receptor (5S rRNA) was prepared. The paramagnetic agent's relaxivity (dependence of the relaxation rate on paramagnetic agent concentration) in the presence and absence of the macromolecular receptor was measured at 1.5 and 6.3 T. The relaxivity of the targeted agent increased specifically in the presence of the macromolecular receptor (16% at 6.3 T and 15% at 1.5 T). This effect was specific for a paramagnetic oligonucleotide targeted to the receptor and was larger than the relaxivity enhancement due simply to receptor-induced viscosity differences. Maximizing this relaxivity enhancement of tumor targeted paramagnetic oligonucleotides will aid in contrast agent development for magnetic resonance imaging.
制备了一种靶向模型大分子受体(5S rRNA)的反义顺磁性寡核苷酸类似物。在存在和不存在大分子受体的情况下,于1.5 T和6.3 T下测量了顺磁性剂的弛豫率(弛豫速率对顺磁性剂浓度的依赖性)。靶向剂的弛豫率在存在大分子受体时特异性增加(6.3 T时为16%,1.5 T时为15%)。这种效应对于靶向受体的顺磁性寡核苷酸是特异性的,并且大于仅由受体诱导的粘度差异导致的弛豫率增强。最大化肿瘤靶向顺磁性寡核苷酸的这种弛豫率增强将有助于磁共振成像造影剂的开发。