Malinowska Katarzyna, Modranka Roman, Majsterek Ireneusz, Misiak Piotr
Pol Przegl Chir. 2014 Apr;86(4):172-6. doi: 10.2478/pjs-2014-0031.
The aim of the study was to analyze the physicochemical synthesized complex 3 [(1,3- thiazol -2- ylimino) methyl)]-4H- chromene -4 -one with tetrachloroplatinate(II) dipotassium and determination peroxidase activity and glutathione (GPX) in red blood cells of cancer patients and healthy subjects.
Tests were carried out with the approval of the Bioethics Committee No. RNN/260/08/KB. Blood was collected into tubes with anticoagulant (heparin lithium). Determination of glutathione peroxidase activity was performed by methods of Little and O'Brien in 20 person groups hospitalized at the Department of General and Colorectal Surgery Veterans General Hospital in Łódź.
The study was an increase of activity in the control without the compound and after the introduction of the complex relative to the treatment groups. In healthy subjects, without the use of glutathione peroxidase complex averaged 73.25 ± 23.88 U / g Hb after application of the compound corresponds to the reference group 81.01 ± 25.94 U / g Hb. In contrast, in patients without the use of the complex activity amounted to 42.85 ± 27.49 U / g Hb. In the study group, which uses synthesized complex GPX activity corresponds to 67.72 ± 13.44 U / g Hb.
The obtained results underline that the introduction of significant blood antioxidant complex research has a significant impact on the results of the determinations. Statistically significant (p < 0.05) difference occurred in both test and no relation to the administration of the complex in relation to the control of 1. 2.
本研究的目的是分析物理化学合成的配合物3[(1,3-噻唑-2-基亚氨基)甲基]-4H-色烯-4-酮与四氯铂酸(II)二钾,并测定癌症患者和健康受试者红细胞中的过氧化物酶活性和谷胱甘肽(GPX)。
本研究经生物伦理委员会第RNN/260/08/KB号批准进行。血液收集到含有抗凝剂(肝素锂)的试管中。谷胱甘肽过氧化物酶活性的测定采用Little和O'Brien的方法,在罗兹退伍军人总医院普通外科和结直肠外科住院的20人组中进行。
研究发现,与治疗组相比,未使用该化合物的对照组和引入该配合物后的活性均有所增加。在健康受试者中,未使用谷胱甘肽过氧化物酶配合物时平均为73.25±23.88 U/g Hb,使用该化合物后对应于参考组的81.01±25.94 U/g Hb。相比之下,未使用该配合物的患者活性为42.85±27.49 U/g Hb。在使用合成配合物的研究组中,GPX活性对应于67.72±13.44 U/g Hb。
所得结果强调,引入显著的血液抗氧化剂配合物研究对测定结果有显著影响。在测试中出现了统计学上显著(p<0.05)的差异,且与配合物的给药无关,与对照组1、2相关。