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首页> 外文期刊>Organic & biomolecular chemistry >Novel polycarboxylated EDTA-type cyclodextrins as ligands for lanthanide binding: study of their luminescence, relaxivity properties of Gd(m) complexes, and PM3 theoretical calculations
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Novel polycarboxylated EDTA-type cyclodextrins as ligands for lanthanide binding: study of their luminescence, relaxivity properties of Gd(m) complexes, and PM3 theoretical calculations

机译:新型多羧化EDTA型环糊精作为镧系元素结合的配体:研究其发光,Gd(m)配合物的弛豫特性和PM3理论计算

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摘要

Novel EDTA-type cyclodextrin (CD) derivatives, AEDTA, BEDTA and GEDTA, bearing 6, 7 and 8 bis(carboxymethyl)amino (iminodiacetic acid) groups, respectively, were prepared, and their complexation with Eu(III), Tb(III) and Gd(III) ions was studied. Luminescence titrations and mass spectrometry showed formation of multimetal complexes (AEDTA 2 to 3, BEDTA mainly 3 and GEDTA exactly 4 metal ions), whereas luminescence lifetime measurements revealed the presence of exchangeable water molecules. Semiempirical quantum mechanical calculations, performed by the PM3 method and assessed by DFT calculations on model ligands, indicated efficient multi-metal complexation, in agreement with the experiment. The structures showed coordination of the metal ions in the outer primary side of the CDs via 4 carboxylate O atoms, 2 N atoms and a glucopyranose O atom per metal ion. Coordination of water molecules was also predicted, in accordance with experimental results. Calculated bond lengths and angles were in agreement with literature experimental values of lanthanide complexes. Calculated energies showed that complex stability decreases in the order GEDTA > BEDTA > AEDTA. ~1H NMR molecular relaxivity measurements for the Gd(III) complexes of AEDTA, BEDTA or GEDTA in water afforded values 4 to 10 times higher than the relaxivity of a commercial contrast agent at 12 MHz, and 6 to 20 times higher at 100 MHz. Solutions of BEDTA and GEDTA Gd(III) complexes in human blood plasma displayed relaxivity values at 100 MHz 7 and 12 times, respectively, higher than the commercial agent. MTT tests of the Gd(III) complexes using human skin fibroblasts did not show toxicity. Attempts to supramolecularly sensitize the luminescence of the lanthanide complexes using various aromatic CD guests were ineffective, evidently due to large guest-metal distances and inefficient inclusion. The described lanthanide complexes, could be useful as contrast agents in MRI.
机译:制备分别带有6、7和8个双(羧甲基)氨基(亚氨基二乙酸)基团的新EDTA型环糊精(CD)衍生物AEDTA,BEDTA和GEDTA,并将其与Eu(III),Tb(III)络合)和Gd(III)离子的研究。发光滴定和质谱分析表明形成了多金属络合物(AEDTA 2至3,BEDTA主要为3,GEDTA正好为4个金属离子),而发光寿命测量表明存在可交换的水分子。通过PM3方法进行的半经验量子力学计算,并通过对模型配体的DFT计算进行评估,表明与实验相符的有效多金属络合。结构表明,每个金属离子通过4个羧基O原子,2个N原子和一个吡喃葡萄糖O原子对CD外部初级侧的金属离子进行配位。根据实验结果,还预测了水分子的配位。计算的键长和角度与镧系元素络合物的文献实验值一致。计算出的能量表明,复合物稳定性按GEDTA> BEDTA> AEDTA的顺序降低。水中AEDTA,BEDTA或GEDTA的Gd(III)配合物的〜1 H NMR分子弛豫度测量值比商用造影剂在12 MHz时的弛豫度高4至10倍,在100 MHz时则高6至20倍。人血浆中BEDTA和GEDTA Gd(III)配合物的溶液在100 MHz处的弛豫值分别比市售试剂高7倍和12倍。使用人皮肤成纤维细胞的Gd(III)配合物的MTT测试未显示毒性。尝试使用各种芳族CD客体来超分子敏化镧系元素络合物的发光是无效的,这显然是由于客体与金属之间的距离较大且夹杂效率低下所致。所描述的镧系元素络合物可用作MRI中的造影剂。

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  • 来源
    《Organic & biomolecular chemistry 》 |2010年第8期| p.1910-1921| 共12页
  • 作者单位

    Institute of Physical Chemistry, National Centre for Scientific Research 'Demokritos', Aghia Paraskevi, 15310, Athens, Greecern;

    Institute of Physical Chemistry, National Centre for Scientific Research 'Demokritos', Aghia Paraskevi, 15310, Athens, Greecern;

    Institute of Materials Science, National Centre for Scientific Research 'Demokritos', Aghia Paraskevi, 15310, Athens, Greecern;

    Institute of Physical Chemistry, National Centre for Scientific Research 'Demokritos', Aghia Paraskevi, 15310, Athens, Greecern;

    Institute of Physical Chemistry, National Centre for Scientific Research 'Demokritos', Aghia Paraskevi, 15310, Athens, Greecern;

    Institute of Physical Chemistry, National Centre for Scientific Research 'Demokritos', Aghia Paraskevi, 15310, Athens, Greecern;

    Istituto di Ricerche Chimiche e Biochimiche 'G. Ronzoni' Citta Studi, via Giuseppe Colombo 81, 20133, Milano, Italyrn;

    Institute of Biology, National Centre for Scientific Research 'Demokritos', Aghia Paraskevi, 15310, Athens, Greecern;

    Institute of Biology, National Centre for Scientific Research 'Demokritos', Aghia Paraskevi, 15310, Athens, Greecern;

    Institute of Physical Chemistry, National Centre for Scientific Research 'Demokritos', Aghia Paraskevi, 15310, Athens, Greece;

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