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用于放化疗研究的 DNA-铂薄膜。

DNA-Platinum Thin Films for Use in Chemoradiation Therapy Studies.

机构信息

Groupe en Sciences des Radiations, Départment de Médecine Nucléaire et Radiobiologie, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, QC, Canada J1H5N4.

出版信息

Bioinorg Chem Appl. 2012;2012:923914. doi: 10.1155/2012/923914. Epub 2011 Oct 2.

Abstract

Dry films of platinum chemotherapeutic drugs covalently bound to plasmid DNA (Pt-DNA) represent a useful experimental model to investigate direct effects of radiation on DNA in close proximity to platinum chemotherapeutic agents, a situation of considerable relevance to understand the mechanisms underlying concomitant chemoradiation therapy. In the present paper we determine the optimum conditions for preparation of Pt-DNA films for use in irradiation experiments. Incubation conditions for DNA platination reactions have a substantial effect on the structure of Pt-DNA in the films. The quantity of Pt bound to DNA as a function of incubation time and temperature is measured by inductively coupled plasma mass spectroscopy. Our experiments indicate that chemical instability and damage to DNA in Pt-DNA samples increase when DNA platination occurs at 37(°)C for 24 hours, the condition which has been extensively used for in vitro studies. Platination of DNA for the formation of Pt-DNA films is optimal at room temperature for reaction times less than 2 hours. By increasing the concentration of Pt compounds relative to DNA and thus accelerating the rate of their mutual binding, it is possible to prepare Pt-DNA samples containing known concentrations of Pt while reducing DNA degradation caused by more lengthy procedures.

摘要

与质粒 DNA 共价结合的铂类化疗药物的干膜代表了一种有用的实验模型,可用于研究辐射对紧邻铂类化疗药物的 DNA 的直接影响,这种情况与理解伴随放化疗治疗的机制密切相关。在本文中,我们确定了用于照射实验的 Pt-DNA 薄膜制备的最佳条件。DNA 铂化反应的孵育条件对薄膜中 Pt-DNA 的结构有很大的影响。通过电感耦合等离子体质谱法测量结合到 DNA 上的 Pt 的量随孵育时间和温度的变化。我们的实验表明,当 DNA 在 37°C 下孵育 24 小时(这是体外研究中广泛使用的条件)时,Pt-DNA 样品中的化学不稳定性和 DNA 损伤会增加。用于形成 Pt-DNA 薄膜的 DNA 铂化在室温下反应时间小于 2 小时时最佳。通过增加相对于 DNA 的 Pt 化合物的浓度,从而加速它们相互结合的速度,可以制备含有已知 Pt 浓度的 Pt-DNA 样品,同时减少由更冗长的程序引起的 DNA 降解。

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