Biomarkers to assess the efficiency of treatment with platinum-based drugs: what can metallomics add?

Since the approval of cisplatin as an antineoplastic drug, the medical and the scientific communities have been concerned about the side effects of platinum-based drugs, and this has been the dose-limiting factor that leads to reduced treatment efficiency. Another important issue is the intrinsic or acquired resistance of some patients to treatment. Identifying proper biomarkers is crucial in evaluating the efficiency of a treatment, assisting physicians in determining, at early stages, whether or not the patient presents resistance to the drug, minimizing severe side effects, and allowing them to redirect the established course of chemotherapy.

Small cetaceans found stranded or accidentally captured in southeastern Brazil: bioindicators of essential and non-essential trace elements in the environment.

Essential (Cu, Mn, Se and Zn) and non-essential (Cd and Hg) elements were analyzed in the hepatic tissue of 22 individuals of seven different species of small cetaceans (Feresa attenuata; Orcinus orca; Pontoporia blainvillei; Sotalia guianensis; Stenella frontalis; Steno bredanensis; Tursiops truncatus) accidentally caught in fishing nets or found stranded along the northern coast of the state of Rio de Janeiro, Brazil, between 2001 and 2010. Atlantic spotted dolphin (S. frontalis) showed the highest levels of Cd (20.

Fish bile as a biomarker for metal exposure.

Fish accumulate several trace elements in muscle, gills and liver, however studies also indicate that metals can be excreted through bile. Since metal contamination leads to modifications in bile composition, biliary excretion offers an alternative way to evaluate the presence of trace-elements. Bile is easier to obtain than other organs and presents a simpler matrix, making it easier for chemical pre-treatment.

Mercury status of the Amazon Continental Shelf: Guiana dolphins (Sotalia guianensis, Van Benédén 1864) as a bioindicator.

Total mercury (Hg) was analyzed in muscle tissue of 27 accidentally captured Guiana dolphins (Sotalia guianensis) in order to evaluate Hg contamination levels present in the Amazon Continental Shelf, in Amapá state, North Brazil. The samples showed a mean concentration of 0.4 ± 0.

Fish metalloproteins as biomarkers of environmental contamination.

Fish are well-recognized bioindicators of environmental contamination. Several recent proteomic studies have demonstrated the validity and value of using fish in the search and discovery of new biomarkers. Certain analytical tools, such as comparative protein expression analyses, both in field and lab exposure studies, have been used to improve the understanding of the potential for chemical pollutants to cause harmful effects.

A novel report of metallothioneins in fish bile: SDS-PAGE analysis, spectrophotometry quantification and metal speciation characterization by liquid chromatography coupled to ICP-MS.

Metallothioneins (MT) are a validated biomarker for metal exposure. In fish they are usually determined in the liver, while some studies have observed MT in kidney, muscle and gills. There are, however, no reports on MT in fish bile.

Guiana dolphins (Sotalia guianensis, Van Benédén 1864) as indicators of the bioaccumulation of total mercury along the coast of Rio de Janeiro state, Southeastern Brazil.

Total mercury (Hg) was determined in muscle tissue of 20 Guiana dolphins stranded along the coast of Rio de Janeiro state, Brazil, with a mean of 1.07 μg/g wet weight. Mercury concentrations were positively related to body length, possibly related to the capacity of the dolphins to bioaccumulate this element throughout life.

Determination of platinum originated from antitumoral drugs in human urine by atomic absorption spectrometric methods.

Cisplatin and carboplatin are the most common platinum-based drugs used in cancer treatment. Pharmacokinetic investigations, the evaluation of the body burden during the treatment, as well as baseline levels of platinum in humans have attracted great interest. Thus, accurate analytical methods for fast and easy Pt monitoring in clinical samples become necessary.

Negligible expression of arsenic in some commercially available brands of Portland cement and mineral trioxide aggregate.

Introduction: This study was designed aiming to determine and compare the amount of arsenic in some brands of mineral trioxide aggregate (MTA) and Portland cement.

Methods: In the present study, arsenic species (As[III], As[V], and dimethylarsinic acid) were separated by high-performance liquid chromatography (HPLC) using a strong anion exchange column and converted into arsines by online HG. The instrumental coupling, HPLC-HG-AFS, was applied to 0.

The use of 2-2-thiazolylazo-p-cresol to minimize the interference of Ni and Cu for the bismuth determination in alloys by hydride generation atomic absorption spectrometry.

Thiazolylazo p-cresol (TAC) was studied as a masking agent for the determination of Bi in rich Ni and Cu alloys by hydride generation atomic absorption spectrometry (HGAAS). In the presence of TAC, Bi/Ni and Bi/Cu ratios up to 1:160 000 and 1:16 000, respectively, were found to be tolerable. No buffering was necessary once the masking agent was effective even in very acid medium.

Direct determination of nickel in petroleum by solid sampling-graphite furnace atomic absorption spectrometry.

A procedure for the direct GFAAS determination of Ni in petroleum samples using a solid sampling strategy is proposed. Palladium was used as conventional modifier. Central composite design multivariate optimization defined the optimum temperature program and the Pd mass, allowing calibration using aqueous analytical solution.

Determination of arsenic in diesel, gasoline and naphtha by graphite furnace atomic absorption spectrometry using microemulsion medium for sample stabilization.

A procedure for the determination of As in diesel, gasoline and naphtha at microg L(-1) levels by GFAAS is proposed. Sample stabilization was achieved by the formation of three component solutions prepared by mixing appropriate volumes of the samples propan-1-ol and nitric acid aqueous solution. This mixture resulted in a one-phase medium, which was indefinitely stable.

The determination of total Se in urine and serum by graphite furnace atomic absorption spectrometry using Ir as permanent modifier and in situ oxidation for complete trimethylselenonium recovery.

The present work evaluated the use of iridium (Ir) as permanent modifier for the determination of total selenium in urine and serum by graphite furnace atomic absorption spectrometry. Concerning urine, the presence of trimethylselenonium (TMSe(+)) was especially considered. Pyrolysis and atomization temperatures of 1,000 and 2,100 degrees C, respectively, were used.