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Physicochemical Properties of Mixed Micellar Aggregates Containing CCK Peptides and Gd Complexes Designed as Tumor Specific Contrast Agents in MRI

机译:含CCK肽和Gd配合物的胶束聚集体的物理化学性质,被设计为MRI中的肿瘤特异性对比剂

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摘要

New amphiphilic molecules containing a bioactive peptide or a claw moiety have been prepared in order to obtain mixed micelles as target-specific contrast agents in magnetic resonance imaging. The first molecule, C_(18)H_(37)CONH(AdOO)_2-G-CCK8 (C18CCK8), contains a C18 hydrophobic moiety bound to the C-terminal cholecystokinin octapeptide amide (CCK 26-33 or CCK8). The second amphiphilic compound, C_(18)H_(37)CONHLys(DTPAGlu)CONH_2 (C18DTPAGlu) or its gadolinium complex, (C18DTPAGlu(Gd)), contains the same C18 hydrophobic moiety bound, through a lysine residue, to the DTPAGlu chelating agent. The mixed aggregates as well as the pure C18DTPAGlu aggregate, in the presence and absence of Gd, have been fully characterized by surface tension measurements, FT-PGSE-NMR, fluorescence quenching, and small-angle neutron scattering measurements. The structural characterization of the mixed aggregates C18DTPAGlu(Gd)-C18CCK8 indicates a spherical arrangement of the micelles with an external shell of ~21 A and an inner core of ~20 A. Both the DTPAGlu(Gd) complexes and the CCK8 peptides point toward the external surface. The measured values for relaxivity in saline medium at 20 MHz proton Larmor frequency and 25 ℃ are 18.7 mM~(-1) s~(-1). These values show a large enhancement in comparison with the isolated DTPAGlu(Gd) complex.
机译:为了在磁共振成像中获得作为目标特异性造影剂的混合胶束,已经制备了含有生物活性肽或爪部分的新型两亲分子。第一个分子C_(18)H_(37)CONH(AdOO)_2-G-CCK8(C18CCK8)包含与C端胆囊收缩素八肽酰胺(CCK 26-33或CCK8)结合的C18疏水部分。第二个两亲化合物C_(18)H_(37)CONHLys(DTPAGlu)CONH_2(C18DTPAGlu)或g络合物(C18DTPAGlu(Gd))包含通过赖氨酸残基与DTPAGlu螯合结合的相同C18疏水部分代理商。在存在和不存在Gd的情况下,混合聚集体以及纯C18DTPAGlu聚集体均已通过表面张力测量,FT-PGSE-NMR,荧光猝灭和小角中子散射测量得到了充分表征。混合聚集体C18DTPAGlu(Gd)-C18CCK8的结构特征表明,胶束的球形排列具有〜21 A的外壳和〜20 A的内核。DTPAGlu(Gd)配合物和CCK8肽都指向外表面。在20 MHz质子拉莫尔频率和25℃下在盐介质中的弛豫测量值为18.7 mM〜(-1)s〜(-1)。与孤立的DTPAGlu(Gd)配合物相比,这些值显示出很大的提高。

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  • 来源
    《Journal of the American Chemical Society》 |2004年第10期|p. 3097-3107|共11页
  • 作者单位

    Centro Interuniversitario per la Ricerca sui Peptidi Bioattivi (CIRPeB) & Department of Biological Chemistry, University of Naples "Federico II" Via Mezzocannone, 6 Naples, I-80134, Italy;

    Centro Interuniversitario per la Ricerca sui Peptidi Bioattivi (CIRPeB) & Department of Biological Chemistry, University of Naples "Federico II" Via Mezzocannone, 6 Naples, I-80134, Italy;

    Department of Chemistry, University of Naples "Federico II" Via Cynthia, Naples, I-80126, Italy;

    of Chemistry IFM,University of Turin, Via Giuria, 7 Turin, I-10125, Italy;

    Department of Chemistry, University of Naples "Federico II" Via Cynthia, Naples, I-80126, Italy;

    Department of Chemistry, University of Naples "Federico II" Via Cynthia, Naples, I-80126, Italy;

    Centro Interuniversitario per la Ricerca sui Peptidi Bioattivi (CIRPeB) & Department of Biological Chemistry, University of Naples "Federico II" Via Mezzocannone, 6 Naples, I-80134, Italy;

    Centro Interuniversitario per la Ricerca sui Peptidi Bioattivi (CIRPeB) & Department of Biological Chemistry, University of Naples "Federico II" Via Mezzocannone, 6 Naples, I-80134, Italy;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

  • 入库时间 2022-08-18 03:24:43

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