VETERİNER DOZAJ FORMUNDA İKİ ANTELMİNTİK İLACIN EŞZAMANLI KANTİTATİF ANALİZİ

Year 2022, , 22 - 30, 19.01.2022

Eda Büker , Nagihan Yaşar , Erdal Dinç

https://doi.org/10.18036/estubtdc.1051707

Abstract

Bu araştırma makalesinde, iki bileşenli bir karışım ve veteriner dozaj formu karışımında ivermektin (IMT)-prezikuantel (PRZQ) miktarının belirlenmesi için yeni bir kromatografik yöntem ultra-performans sıvı kromatografisi (UPLC) yöntemi geliştirilmiştir. İncelenen veteriner ilaçlarının (IMT ve PRZQ) ayrılması, su-asetonitril-metanolden (10:70:20, v/v). Kromatografik analizde akış hızı 0.38 mL/dk idi ve kolon sıcaklığı 42 0C'de tutuldu. IMT ve PRZQ'nun kromatografik tespiti sırasıyla 220.0 ve 245.0 nm dalga boyunda yapıldı. Geliştirilen UPLC yöntemi valide edilmiş ve IMT ve PRZQ'dan oluşan gerçek örneklere uygulanmıştır. Geri kazanım tahlil sonuçlarının PRZQ için %100.4 ve IMT için %101.8 olduğu bulundu. Sunulan UPLC yöntemi, bu ilaçları içeren farmasötik preparasyonların kalite kontrolü için alternatif bir seçenek olarak sunulmuştur. Bu ilaçları içeren farmasötik preparatların kalite kontrolü için, alternatif bir deneysel analiz seçeneği olarak sunulan UPLC yöntemi tanıtılmıştır.

Keywords

Ultra performance liquid chromatography, ivermectin, praziquantel, anthelmintic veterinary dosage form

SIMULTANEOUS QUANTITATIVE ANALYSIS OF TWO ANTHELMINTIC DRUGS IN A VETERINARY DOSAGE FORM

Abstract

In this research article, a new chromatographic method ultra-performance liquid chromatography (UPLC) method was developed for the quantification of ivermectin (IMT)-preziquantel (PRZQ) in a two-component mixture and veterinary dosage form mixture. The separation of the studied veterinary drugs (IMT and PRZQ) was carried out on Waters Acquity ® BEH C18 column (50mm x 2.1 mm i.d., 1.7 m) using a mobile phase consisting of water-acetonitrile-methanol (10:70:20, v/v). In the chromatographic analysis, flow rate was 0.38 mL/min, and column temperature was maintained at 42 0C. The chromatographic detection of IMT and PRZQ was made at the wavelength of 220.0 and 245.0 nm, respectively. The developed UPLC method was validated and applied to real samples consisting of IMT and PRZQ. Recovery assay results were found to be 100.4 % for PRZQ and 101.8 % for IMT. The presented UPLC method is introduced as an alternative choice for the quality control of pharmaceutical preparations containing these drugs. For the quality control of pharmaceutical preparations containing these drugs, the presented UPLC method is introduced as an alternative experimental analysis choice.

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