KMID : 1023520220450030243
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Korean Journal of Veterinary Service 2022 Volume.45 No. 3 p.243 ~ p.248
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A HPLC-UV method for quantification of ivermectin in solution from veterinary drug products
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Kim Young-Wook
Jeong Woo-Seog
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Abstract
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The HPLC conditions for analysis of ivermectin in solutions dosage forms of commercial anthelmintics are different for each product. The purpose of this study was to establish a standardized chromatographic method for the quantification of ivermectin in solution. The separation was achieved on Waters Xbridge C18 column (4.6¡¿150 nm, 5 §) using different kinds of mobile phase composed of water/methanol/acetonitrile (15/34/51, v/v and 19.5/27.5/53, v/v), with UV detection at wavelengths 245 nm and 254 nm. A total of five commercial ivermectin in solution samples were analyzed. In this study, the optimal chromatographic conditions for analysis of ivermectin in solution were mobile phase of water/methanol/acetonitrile (15/34/51, v/v) at a flow rate of 1.0 mL/min and a detection wavelength of 245 nm using a Waters Xbridge C18 column (4.6¡¿250 nm, 5 §) at a column temperature of 25¡É. The linearity was observed in the concentration range of 50~150 §¶/mL, with a correlation coefficient, r2= 0.99999. The limit of detection and the limit of quantification were 0.88 and 2.68 §¶/mL, respectively. The accuracy (% recovery) was found to be 98.9 to 100.3%. Intra-day and Intermediate precisions with relative standard deviations were less than 1.0%. The content of ivermectin for five market samples ranged 91.2~102.7%. The proposed method was also found to be robust, therefore, the method can be used for the routine analysis of ivermectin in solutions dosage forms.
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KEYWORD
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Ivermectin, Veterinary, HPLC, Validation
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