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Design of Experiment-Based Green UPLC-DAD Method for the Simultaneous Determination of Indacaterol, Glycopyrronium and Mometasone in their Combined Dosage Form and Spiked Human Plasma
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Abstract
Indacaterol, is an ultra-long-acting β2 agonist, glycopyrronium is a long-acting muscarinic-antagonist and mometasone is a synthetic corticosteroid. They were used recently in combination for the treatment of severe asthma symptoms and chronic obstructive pulmonary disease. In this work, it was the first time to develop a green and environment friendly ultra-performance liquid chromatographic method using design expert program for the analysis of the three drugs in their combined dosage form. Also, the method was bioanalytically validated for the analysis of the three drugs in spiked human plasma samples. The method was linear in range from 0.50 to 100.0 μg mL−1 for indacaterol and mometasone and from 1.0 to 150.0 μg mL−1 for glycopyrronium. It showed high accuracy where, the % recovery for indacaterol, glycopyrronium and mometasone in plasma were ranged from 94.27 to 97.86%, 96.43 to 98.75% and 96.86 to 98.43%, respectively. Also, it was precise where, the % relative standard deviation for the inter-day precision was ranged from 2.571 to 3.484%, 3.180 to 4.123% and 3.150 to 3.984% and the intra-day precision was ranged from 2.351 to 3.125%, 2.512 to 3.544% and 2.961 to 3.983% for indacaterol, glycopyrronium and mometasone, respectively. The limit of detection and the limit of quantification for indacaterol and mometasone were 0.03 and 0.10 μg mL−1 while for glycopyrronium, they were 0.16 and 0.50 μg mL−1.
Highlights
Oxford University Press (OUP)
Title: Design of Experiment-Based Green UPLC-DAD Method for the Simultaneous Determination of Indacaterol, Glycopyrronium and Mometasone in their Combined Dosage Form and Spiked Human Plasma
Description:
Abstract
Indacaterol, is an ultra-long-acting β2 agonist, glycopyrronium is a long-acting muscarinic-antagonist and mometasone is a synthetic corticosteroid.
They were used recently in combination for the treatment of severe asthma symptoms and chronic obstructive pulmonary disease.
In this work, it was the first time to develop a green and environment friendly ultra-performance liquid chromatographic method using design expert program for the analysis of the three drugs in their combined dosage form.
Also, the method was bioanalytically validated for the analysis of the three drugs in spiked human plasma samples.
The method was linear in range from 0.
50 to 100.
0 μg mL−1 for indacaterol and mometasone and from 1.
0 to 150.
0 μg mL−1 for glycopyrronium.
It showed high accuracy where, the % recovery for indacaterol, glycopyrronium and mometasone in plasma were ranged from 94.
27 to 97.
86%, 96.
43 to 98.
75% and 96.
86 to 98.
43%, respectively.
Also, it was precise where, the % relative standard deviation for the inter-day precision was ranged from 2.
571 to 3.
484%, 3.
180 to 4.
123% and 3.
150 to 3.
984% and the intra-day precision was ranged from 2.
351 to 3.
125%, 2.
512 to 3.
544% and 2.
961 to 3.
983% for indacaterol, glycopyrronium and mometasone, respectively.
The limit of detection and the limit of quantification for indacaterol and mometasone were 0.
03 and 0.
10 μg mL−1 while for glycopyrronium, they were 0.
16 and 0.
50 μg mL−1.
Highlights.
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