Development and validation of an analytical method for the simultaneous determination of the alcohol biomarkers ethyl glucuronide, ethyl sulfate, N‐acetyltaurine, and 16:0/18:1‐phosphatidylethanol in human blood

Abstract A rapid, simple, and sensitive RP-HPLC analytical method was developed for the simultaneous determination of triclabendazole and ivermectin in combination using a C18 RP column. The mobile phase was acetonitrilemethanolwateracetic acid (56 36 7.5 0.5, v/v/v/v) at a pH of 4.35 and flow rate of 1.0 mL/min. A 245 nm UV detection wavelength was used. Complete validation, including linearity, accuracy, recovery, LOD, LOQ, precision, robustness, stability, and peak purity, was performed. The calibration curve was linear over the range 50.09150.26 g/mL for triclabendazole with r = 0.9999 and 27.0181.02 g/mL for ivermectin with r = 0.9999. Calculated LOD and LOQ for triclabendazole were 0.03 and 0.08 g/mL, respectively, and for ivermectin 0.07 and 0.20 g/mL, respectively. The intraday precision obtained was 98.71 with RSD of 0.87 for triclabendazole and 100.79 with RSD 0.73 for ivermectin. The interday precision obtained was 99.51 with RSD of 0.35 for triclabendazole and 100.55 with RSD of 0.59 for ivermectin. Robustness was also studied, and there was no significant variation of the system suitability of the analytical method with small changes in experimental parameters.

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Analytical Method Development and Validation for Telmisartan, Chlorthalidone and Amlodipine by UV- Spectroscopic Method.

Research Journal of Pharmacy and Technology ◽

10.52711/0974-360x.2021.01051 ◽

2021 ◽

pp. 6049-6054

Author(s):

Rutuja M. Sanap ◽

Sarika R. Wavhale ◽

Vaibhavi V. Kunjir ◽

Rajkumar V. Shete

Keyword(s):

Simultaneous Determination ◽

Analytical Method ◽

Dosage Form ◽

Method Development ◽

Correction Method ◽

Absorption Correction ◽

Method Development And Validation ◽

Development And Validation ◽

Tablet Dosage

A simple, sensitive and accurate UV- spectrophotometric absorption correction method has been developed for simultaneous determination of Telmisartan, Amlodipine and Chlorthalidone in combined tablet dosage form. Analytical method development and validation plays important role in the discovery manufacture of pharmaceuticals and development. In this paper, absorption correction method is used for multi-component analysis. The wavelengths selected for the analysis were 311nm for Telmisartan, 228nm for Chlorthalidone and 253nm for Amlodipine. Beer’s law obeyed the concentration range of 2-10 µg /ml, 2-10 µg /ml and 5-25 µg/ ml for Telmisartan, Amlodipine and Chlorthalidone. Methanol is used as a solvent. The accuracy of the method was assessed by recovery studies and was found between the range of 100% to 110% for Telmisartan, 85% to 110% for Amlodipine and 85% to 105% Chlorthalidone. The % RSD value was found to be less than 2. Thus, the method was simple, precise, economic, rapid, accurate and can be successfully applied for simultaneous determination of Telmisartan, Amlodipine and Chlorthalidone in combined tablet dosage form.

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