HPLC method for simultaneous determination of salmeterol xinafoate and fluticasone propionate for the quality control of dry powder inhalation products-Reference-Cited by-同舟云学术

HPLC method for simultaneous determination of salmeterol xinafoate and fluticasone propionate for the quality control of dry powder inhalation products

Published:2015-06 Issue:2 Volume:27 Page:309-320
ISSN:1233-2356
Container-title:Acta Chromatographica
language:en
Short-container-title:Acta Chromatographica

Author:

Pączkowska E.,Smukowska D.,Tratkiewicz E.,Białasiewicz P.

Publisher

Akademiai Kiado Zrt.

Subject

General Chemistry

Link

https://www.akademiai.com/doi/pdf/10.1556/achrom.27.2015.2.8

Reference13 articles.

1. European Pharmacopoeia, EDQM, 2011. http://www.edqm.eu

2. Committee for Medicinal Products for Human Use (CHMP), European Medicines Agency, London, 2009. Guideline on the Requirements for Clinical Documentation for Orally Inhaled Products (OIP) Including the Requirements for Demonstration of Therapeutic Equivalence between Two Inhaled Products for Use in the Treatment of Asthma and Chronic Obstructive Pulmonary Disease (COPD) in Adults and for Use in the Treatment of Asthma in Children And Adolescents

3. The physico-chemical properties of salmeterol and fluticasone propionate in different solvent environments

4. Validation of a reverse-phase high performance liquid chromatographic method for concurrent assay of a weak base (salmeterol xinafoate) and a pharmacologically active steroid (fluticasone propionate)

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