期刊
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 387, 期 8, 页码 2815-2822出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s00216-007-1147-9
关键词
metal speciation; carboplatin; protein complexation; SEC-ICP-MS
资金
- NCI NIH HHS [CA66077] Funding Source: Medline
- NIEHS NIH HHS [P30 ES005022, ES05022] Funding Source: Medline
To study the carboplatin-protein interaction, a sensitive method using size exclusion chromatography coupled to inductively coupled plasma mass spectrometry (SEC-ICP-MS) was developed. The complexes formed between plasma proteins and carboplatin were monitored and identified with this method. Composite blood plasma samples from patients who were undergoing chemotherapy were analyzed, and carboplatin was found to bind plasma proteins. In addition, blank plasma samples were spiked with carboplatin and were analyzed as a time course study, and the results confirmed that carboplatin formed complexes with plasma proteins, primarily albumin and gamma-globulin. To further substantiate the study, these two proteins were incubated with carboplatin. The binding between carboplatin and these proteins was then characterized qualitatively and quantitatively. In addition to a one-to-one binding of Pt to protein, protein aggregation was observed. The kinetics of the binding process of carboplatin to albumin and gamma-globulin was also studied. The initial reaction rate constant of carboplatin binding to albumin was determined to be 0.74 M-1 min(-1), while that for gamma-globulin was 1.01 M-1 min(-1), which are both lower than the rate constant of the cisplatin-albumin reaction previously reported.
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