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新型体外高细胞毒性铂和钯氰氧基配合物,体内副作用极小。

New in vitro highly cytotoxic platinum and palladium cyanoximates with minimal side effects in vivo.

机构信息

Department of Chemistry, Temple Hall 431, Missouri State University, 901 S. National, Springfield, MO 65897, USA.

Department of Biology, Missouri State University, MC/Center for Biomedical & Life Sciences, Springfield, MO 65897, USA.

出版信息

J Inorg Biochem. 2020 Jul;208:111082. doi: 10.1016/j.jinorgbio.2020.111082. Epub 2020 May 6.

Abstract

Several biologically active bivalent Pd and Pt complexes with two structurally similar cyanoxime ligands abbreviated as H(DECO): 2-oximino-2-cyano-N,N'-diethylacetamide, and H(PyrCO): 2-oximino-2-cyan-N-pyrrolidine acetamide were synthesized and characterized using spectroscopic methods, thermal analysis and X-ray crystallography. Structures revealed planar cis-geometry of studied complexes. Freshly obtained Pt(DECO), Pd(DECO), Pt(PyrCO) and Pd(PyrCO) complexes were used in for in vitro cytotoxicity assays using two different etiology human cancer cell lines HeLa and WiDr cells. Investigated compounds showed cytotoxicity levels at or above cisplatin. Pt(DECO) was also tested in vivo in healthy C57BL/6 mice. The complex was administered at three different dosage (0, 7.5, 15 mg/kg, i.p. once/week), over a total period of 8 weeks. No changes were observed in the animal weight in the treated mice compared to the control dextrose-treated group. The levels of erythrocytes, leukocytes, and hemoglobin were within the normal level suggesting low myelotoxicity. Negligible cardiotoxicity was observed from the histological evaluation of the hearts from the treated animals. Results from the tail nerve conduction velocity (NCV) and nerve histomorphometry suggested no impact of Pt(DECO) on peripheral nerves. The complex, however, induced certain hepatotoxicity and lead to the elevation of IL-6, a pro-inflammatory cytokine. Overall, Pt(DECO)2 showed minimal in vivo toxicity, thus presenting a promising candidate for future testing in animal models of cancer.

摘要

几种具有两个结构相似的氰肟配体的生物活性双价 Pd 和 Pt 配合物,缩写为 H(DECO):2-肟基-2-氰基-N,N'-二乙酰胺和 H(PyrCO):2-肟基-2-氰基-N-吡咯烷乙酰胺,已通过光谱法、热分析和 X 射线晶体学进行了合成和表征。结构揭示了研究配合物的平面顺式几何形状。新获得的 Pt(DECO)、Pd(DECO)、Pt(PyrCO)和 Pd(PyrCO)配合物用于使用两种不同病因的人类癌细胞系 HeLa 和 WiDr 细胞进行体外细胞毒性测定。研究的化合物表现出与顺铂相当或更高的细胞毒性水平。Pt(DECO)也在健康 C57BL/6 小鼠体内进行了测试。该复合物以三种不同剂量(0、7.5、15mg/kg,腹腔注射,每周一次)给药,总共 8 周。与对照葡萄糖处理组相比,治疗小鼠的动物体重没有变化。红细胞、白细胞和血红蛋白水平均在正常范围内,表明骨髓毒性较低。从治疗动物的心脏组织学评估中观察到可忽略不计的心脏毒性。尾部神经传导速度 (NCV) 和神经形态计量学的结果表明,Pt(DECO)对周围神经没有影响。然而,该复合物会引起一定的肝毒性,并导致促炎细胞因子 IL-6 的升高。总的来说,Pt(DECO)2 表现出最小的体内毒性,因此是未来在癌症动物模型中进行测试的有前途的候选物。

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