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1.
Figure

Figure. From: Arsenic speciation in saliva of acute promyelocytic leukemia patients undergoing arsenic trioxide treatment.

Arsenic species and temporal profiles over three days from nine patients

Baowei Chen, et al. Anal Bioanal Chem. 2013;405(6):1903-1911.
2.
Fig. 3

Fig. 3. From: Arsenic speciation in saliva of acute promyelocytic leukemia patients undergoing arsenic trioxide treatment.

A chromatogram obtained from HPLC–ICPMS analysis of an H2O2-treated chromatographic fraction containing MMAIII. Peak identities and HPLC–ICPMS conditions are the same as those for Fig. 

Baowei Chen, et al. Anal Bioanal Chem. 2013;405(6):1903-1911.
3.
Fig. 2

Fig. 2. From: Arsenic speciation in saliva of acute promyelocytic leukemia patients undergoing arsenic trioxide treatment.

Chromatograms of saliva samples and the same samples spiked with authentic arsenic standards. Peak identities and high-performance liquid chromatography (HPLC)–ICPMS conditions were the same as those for Fig. . A chromatograms were obtained from a saliva sample (solid trace) and the same sample spiked with authentic MMAIII (dashed trace). B chromatograms were obtained from a saliva sample (solid trace) and the same sample spiked with MMMTAV (dashed trace)

Baowei Chen, et al. Anal Bioanal Chem. 2013;405(6):1903-1911.
4.
Fig. 6

Fig. 6. From: Arsenic speciation in saliva of acute promyelocytic leukemia patients undergoing arsenic trioxide treatment.

Temporal profiles showing the percentages of methylated arsenicals in the saliva of APL patient 4 (a) and patient 6 (b). The procedures for arsenic administration were the same as described for Fig. . Triangles MMAV, circles DMAV, diamonds sum of methylated arsenic

Baowei Chen, et al. Anal Bioanal Chem. 2013;405(6):1903-1911.
5.
Fig. 4

Fig. 4. From: Arsenic speciation in saliva of acute promyelocytic leukemia patients undergoing arsenic trioxide treatment.

Chromatogram obtained from HPLC–electrospray ionization tandem mass spectrometry (ESI-MS/MS) analysis of synthesized MMMTAV standard. Anion-exchange separation was performed using a Hamilton PRP-X100 column and a mobile phase comprising 50 % methanol and 5 mM ammonium formate (pH 6). ESI-MS/MS was performed in multiple reaction monitoring mode. Three characteristic ion transitions, 155/107, 155/121, and 155/137, of MMMTAV were monitored simultaneously

Baowei Chen, et al. Anal Bioanal Chem. 2013;405(6):1903-1911.
6.
Fig. 5

Fig. 5. From: Arsenic speciation in saliva of acute promyelocytic leukemia patients undergoing arsenic trioxide treatment.

Temporal profiles showing the concentrations of arsenic species in the saliva of APL patients. The patients received an intravenous infusion of a 10 mg dose of arsenic trioxide daily. The arrows indicate the time at which the infusion started. Collection of saliva samples from patient 4 (a) lasted 72 h with three arsenic (AsIII) administrations of long infusion duration (about 18 h), and saliva samples from patient 6 (b) were collected for 52 h with two administrations of short infusion duration (below 4 h). Squares AsIII, circles DMAV, upright triangles MMAV, inverted triangles AsV, diamonds sum of arsenic species

Baowei Chen, et al. Anal Bioanal Chem. 2013;405(6):1903-1911.
7.
Fig. 1

Fig. 1. From: Arsenic speciation in saliva of acute promyelocytic leukemia patients undergoing arsenic trioxide treatment.

Typical chromatograms of arsenic standards (A) and saliva samples (B) from acute promyelocytic leukemia (APL) patients. Separation was achieved using a reversed-phase ODS-3 column, and a mobile phase comprising 5 mM tetrabutylammonium, 3 mM malonic acid, and 5 % methanol (pH 5.65). Arsenic was detected at m/z 75 using an Agilent 7500ce inductively coupled plasma mass spectrometry (ICPMS) instrument with an octopole reaction system. Peaks 18 correspond to AsIII, monomethylarsonous acid (MMAIII), dimethylarsinic acid (DMAV), monomethylarsonic acid (MMAV), dimethylmonothioarsonic acid, dimethylarsinous acid (DMAIII), AsV, and monomethylmonothioarsonic acid (MMMTAV), respectively

Baowei Chen, et al. Anal Bioanal Chem. 2013;405(6):1903-1911.

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