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A simple and green liquid chromatography method for the determination of ibuprofen in milk-containing simulated gastrointestinal media for monitoring the dissolution studies of three-dimensional-printed formulations.
Doumtsi, Antigoni; Manousi, Natalia; Karavasili, Christina; Fatouros, Dimitrios G; Tzanavaras, Paraskevas D; Zacharis, Constantinos K.
Afiliação
  • Doumtsi A; Department of Pharmaceutical Technology, Laboratory of Pharmaceutical Analysis, School of Pharmacy, Aristotle University of Thessaloniki, Thessaloniki, Greece.
  • Manousi N; Department of Chemistry, Laboratory of Analytical Chemistry, Faculty of Sciences, Aristotle University of Thessaloniki, Thessaloniki, Greece.
  • Karavasili C; Department of Pharmacy, Laboratory of Pharmaceutical Technology, Aristotle University of Thessaloniki, Thessaloniki, Greece.
  • Fatouros DG; Department of Pharmacy, Laboratory of Pharmaceutical Technology, Aristotle University of Thessaloniki, Thessaloniki, Greece.
  • Tzanavaras PD; Department of Chemistry, Laboratory of Analytical Chemistry, Faculty of Sciences, Aristotle University of Thessaloniki, Thessaloniki, Greece.
  • Zacharis CK; Department of Pharmaceutical Technology, Laboratory of Pharmaceutical Analysis, School of Pharmacy, Aristotle University of Thessaloniki, Thessaloniki, Greece.
J Sep Sci ; 45(21): 3955-3965, 2022 Nov.
Article em En | MEDLINE | ID: mdl-36054076
ABSTRACT
A fast and green ultra-high-performance liquid chromatographic method was developed for the determination of ibuprofen in milk-containing simulated gastrointestinal media to monitor the dissolution of three-dimensional printed formulations. To remove interfering compounds, protein precipitation using methanol as a precipitation reagent was performed. The separation of the target analyte was performed on a C18 column using a mobile phase consisting of 0.05% v/v aqueous phosphoric acid solution methanol, 2575% v/v. Method validation was conducted using the total error concept. The ß-expectation tolerance intervals did not exceed the acceptance criteria of ±15%, meaning that 95% of future results will be included in the defined bias limits. The relative bias ranged between ─1.1 and +3.2% for all analytes, while the relative standard deviation values for repeatability and intermediate precision were less than 2.8% and 3.9%, respectively. The achieved limit of detection was 0.01 µg/ml and the lower limit of quantitation was established as 2 µg/ml. The proposed method was simple, and it required reduced organic solvent consumption following the requirements of Green Analytical Chemistry. The method was successfully employed for the determination of ibuprofen in real biorelevant media obtained from dissolution studies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ibuprofeno / Leite Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ibuprofeno / Leite Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article