Fluorometric Determination of Artemisinin Using the Pyronin B–Microperoxidase-11 System
- Authors: Muginova S.V.1, Vakhraneva E.S.1, Myasnikova D.A.2, Shekhovtsova T.N.1
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Affiliations:
- Moscow State University
- Yokohama National University
- Issue: Vol 74, No 2 (2019)
- Pages: 100-107
- Section: Articles
- URL: https://journals.rcsi.science/1061-9348/article/view/183137
- DOI: https://doi.org/10.1134/S1061934818120079
- ID: 183137
Cite item
Abstract
A sensitive, rapid, and simple fluorimetric procedure for the determination of artemisinin in a concentration range of 0.1–7 μM was developed with the use of microperoxidase-11 as a peroxidase biomimetic (RSD = 0.8% at LOQ, n = 5; LOD = 7.1 nM (3s0)). The determination is based on the fluorescence quenching of the cationic xanthene dye pyronin B (Stern–Volmer quenching constant, 0.101 μM–1) in the presence of microperoxidase-11. The procedure was tested in the analysis of a biologically active additive based on an Artemisia annua wormwood extract. The correctness of the results of the fluorimetric determination of artemisinin in a biologically active dietary supplement was confirmed by HPLC–mass spectrometry. The use of oligopeptide microperoxidase-11 instead of heme-containing proteins (hemoglobin, cytochrome c, and horseradish peroxidase) made it possible to shorten the duration of artemisinin determination by a factor of 2 with the retention of sensitivity and selectivity.
Keywords
About the authors
S. V. Muginova
Moscow State University
Email: tnshekh@yandex.ru
Russian Federation, Moscow, 119991
E. S. Vakhraneva
Moscow State University
Email: tnshekh@yandex.ru
Russian Federation, Moscow, 119991
D. A. Myasnikova
Yokohama National University
Email: tnshekh@yandex.ru
Japan, 79-5 Tokiwadai, Hodogaya-ku, Yokohama, 240-8501
T. N. Shekhovtsova
Moscow State University
Author for correspondence.
Email: tnshekh@yandex.ru
Russian Federation, Moscow, 119991
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