Advanced search
Start date
Betweenand
Related content
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Microwave-assisted sample preparation of medicines for determination of elemental impurities in compliance with United States Pharmacopeia: How simple can it be?

Full text
Author(s):
Pinheiro, Fernanda C. [1] ; Barros, I, Ariane ; Nobrega, Joaquim A. [2]
Total Authors: 3
Affiliation:
[1] Univ Fed Sao Carlos, Grp Appl Instrumental Anal, Dept Chem, POB 676, BR-13560270 Sao Carlos, SP - Brazil
[2] Barros, Ariane, I, Univ Fed Sao Carlos, Grp Appl Instrumental Anal, Dept Chem, POB 676, BR-13560270 Sao Carlos, SP - Brazil
Total Affiliations: 2
Document type: Journal article
Source: Analytica Chimica Acta; v. 1065, p. 1-11, AUG 13 2019.
Web of Science Citations: 2
Abstract

This work proposed a procedure for microwave-assisted sample preparation of medicines using diluted nitric acid followed by determination of elemental impurities using inductively coupled plasma optical emission spectrometry (ICP OES) and inductively coupled plasma mass spectrometry (ICP-MS) according to the United States Pharmacopeia Chapters 232 and 233. Three solutions, i.e. inverse aqua regia, 7.0 and 2.0 mol L-1 HNO3, were evaluated for microwave-assisted digestion of nine drugs samples. The applicability of each digestion procedure was assessed by comparison of analyte concentrations determined using total (reference procedure) and partial digestions (proposed procedure) as well as by determining dissolved carbon content and evaluating matrix effects. There were none significant differences at a 95% confidence level among the concentrations determined applying reference and proposed procedures. Internal standardization (ICP OES) and aerosol dilution (ICP-MS) were applied for minimization and correction of matrix effects. Addition and recovery experiments were performed according to oral permissible daily exposures values specific for each element and each sample was spiked with element concentrations of 0.5J and 1.5J in order to check accuracies for 24 analytes. Recoveries ranged from 70 to 138% for ICP OES and from 72 to 128% for ICP-MS, for all elements but Os. All analytes were below the respective limits of quantification when applying all sample preparation procedures, except As, Ba, Co, Cu, Cr, Mo, Ni, Pb, Sb, Sn, TI and V, however the determined concentrations for these elements were lower than the limits proposed by Chapter 232. (C) 2019 Elsevier B.V. All rights reserved. (AU)

FAPESP's process: 14/50951-4 - INCT 2014: Advanced Analytical Technologies
Grantee:Celio Pasquini
Support Opportunities: Research Projects - Thematic Grants