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Micelle-Incorporated Liquid Chromatography in the Light of Green Chemistry: An Application for the Quality Control Analysis of Anti-Platelet Fixed-Dose Combinations.
Elsonbaty, Ahmed; Hassan, Wafaa S; Eissa, Maya S; Abdulwahab, Sara.
Afiliação
  • Elsonbaty A; Egyptian Russian University, Faculty of Pharmacy, Department of Analytical Chemistry, Cairo, Egypt.
  • Hassan WS; Zagazig University, Faculty of Pharmacy, Department of Analytical Chemistry, Zagazig, Egypt.
  • Eissa MS; Egyptian Russian University, Faculty of Pharmacy, Department of Analytical Chemistry, Cairo, Egypt.
  • Abdulwahab S; Zagazig University, Faculty of Pharmacy, Department of Analytical Chemistry, Zagazig, Egypt.
J AOAC Int ; 105(5): 1228-1233, 2022 Sep 06.
Article em En | MEDLINE | ID: mdl-35595172
ABSTRACT

BACKGROUND:

Oral anti-platelet agents are the cornerstone of the treatment of multiple cardiovascular diseases and in the long-term prevention of their recurrence.

OBJECTIVE:

In the present work, we report a method based on micellar liquid chromatography coupled with ultraviolet detection (MLC/UV), for the simultaneous quantification of combined anti-platelet therapy namely, clopidogrel bisulfate (CPS), aspirin (ASP), together with salicylic acid (SA), in their pharmaceutical dosage form.

METHODS:

The incorporation of 0.1M polyoxyethylene 23 lauryl ether (Brij-35) as a surfactant into the mobile phase improved solute-mobile phase interaction allowing for minimal organic solvent utilization, enhanced resolution, and rapid analysis (7 min). Furthermore, we performed a comprehensive evaluation of the environmental impact caused by our procedures versus previously reported analytical procedures applied in the determination of CPS and ASP. The evaluation was made using the Eco-scale tool.

RESULTS:

The results of the developed method indicated the superiority of our procedures in terms of greenness without compromising the quality of performance characteristics. The method was linear in the range of 1-100 µg/mL with limits of detection of 0.28, 0.32, and 0.29 µg/mL for CPS, ASP, and SA, respectively. The developed method can also be utilized to test the purity and the stability of ASP in pharmaceutical formulations through monitoring SA as its main degradation product.

CONCLUSION:

The MLC/UV method was successfully applied to the quantitative analysis of CPS, ASP together with SA-as a main degradation product of ASP-in their pharmaceutical dosage form. HIGHLIGHTS The developed method was successfully applied for the determination of clopidogrel bisulfate (CPS), aspirin (ASP), together with salicylic acid (SA), in their pharmaceutical dosage form.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácido Salicílico / Micelas Idioma: En Revista: J AOAC Int Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Egito

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácido Salicílico / Micelas Idioma: En Revista: J AOAC Int Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Egito