SPECTROPHOTOMETRIC DETERMINATION OF PIPERIDINE 7-PROPYL-3-METHYLXANTHINE-8-YLTHIOACETATE
DOI:
https://doi.org/10.11603/2312-0967.2022.4.13735Keywords:
piperidine 7-propyl-3-methylxanthine-8-ylthioacetate, quantitative determination, UV spectrophotometry, validationAbstract
The aim of the work. Development and validation of UV spectrophotometric method for the quantitative determination of piperidine 7-propyl-3-methylxanthine-8-ylthioacetate.
Materials and Methods. The object of the study is a substance of piperidine 7-propyl-3-methylxanthine-8-ylthioacetate. The solvent – purified water. Analytical equipment: Specord 200 spectrophotometer (Analytic Jena AG, Germany), electronic laboratory scales (RADWAG XA 210.4Y), the ultrasonic bath (Sonorex Digitec DT100H), measuring utensils (Class A).
Results and Discussion. The band observed at 260–340 nm with a maximum of light absorption at 295 nm was selected to develop the method for the quantitative determination of this substance. According to the requirements of the SPU, the forecast of complete uncertainty of the methodology was calculated, as well as the validation of the methodology according to such validation characteristics as range of application, linearity, precision, accuracy and robustness. The range of application of the technique is in the range of 60–140 %. The calculated numerical values of linear dependence indicate that the method is linear in the whole range of application methods. The calculated confidence interval does not exceed the maximum allowable uncertainty of the analysis, which indicates that the method is accurate at the level of convergence. It is proved that the systematic error δ, which is introduced by the instability of the analyzed solution, does not exceed the critical value of maxδ, ie the solution remains stable for at least 1 hour.
Conclusion. The UV spectrophotometric method for the quantitative determination of piperidine 7-propyl-3-methylxanthine-8-ylthioacetate has been developed and validated.
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