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E. I. Montero, J. M. Perez, A. Schwartz, M. A. Fuertes, J. M. Maligne, C. Alonso, M. Leng and C. Navarro-Ranninger, “Apoptosis Induction and DNA Interstrand Cross- Link Formation by Citotoxic Trans- [PtCl2(NH(CH3)2(NH2(CH(CH3)2]: Cross-Linking between d(G) and Complementary d(G) within Oligonucleotide Duplexes,” Biochemistry (Chemical Biology), Vol. 3, No. 1, 2002, pp. 101-107. doi:10.1002/1439-7633(20020104)3:1<61::AID-CBIC61>3.0.CO;2-I

has been cited by the following article:

• TITLE: Use of Cucurbit [6] Uril as a Modifier in the Electrochemical Determination of Antitumor Platinum (II) Complex: Trans-[PtCl2(Dimethylamine) (Isopropylamine)]. Application to Biological Samples

  AUTHORS: Carmen S. H. Domínguez, Pedro Hernández

  KEYWORDS: Trans-[PtCl2(Dimethylamine)(Isopropylamine)]; Differential Pulse Voltammetry (DPV); Square Wave Voltammetry (SWV); Biological Fluids; Human Urine

  JOURNAL NAME: American Journal of Analytical Chemistry, Vol.4 No.6, June 20, 2013

  ABSTRACT: A square wave voltammetry (DPV) method for trans-Pt[Cl2(Dimethylamine)(isopropylamine)] determination is developed. To this end, all the chemical and instrumental variables affecting the determination of trans-Pt[Cl2(Dimethylamine) (isopropylamine)] are optimized. From studies of the mechanisms governing the electrochemical response of trans-Pt[Cl2(Dimethylamine)(isopropylamine)], it was concluded that it was an electrochemically reversible system with an adsorptive oxidation phenomenon. Under optimal conditions, the variation of analytical signal (Ip) with trans-Pt[Cl2(Dimethylamine)(isopropylamine)] concentration was linear in the 0.05 μg·mL-1 to 10 μg·mL-1 range, with a LOD 91 μg·mL-1 of and a LOQ of 303 μg·mL-1, a RSD 1.10% and Er 0.72%. The optimized method was applied to the determination of trans-Pt[Cl2(Dimethylamine)(isopropylamine)] in biological fluids, in human urine and synthetic urine.