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Название: | Development and validation of a new spectrophotometric method for the determination of gabapentin in capsules |
Авторы: | Miedviedieva, K. P. Vasyuk, S. O. Portna, O. O. Мєдвєдєва, Катерина Павлівна Васюк, Світлана Олександрівна Портна, Олена Олексіївна |
Ключевые слова: | spectrophotometry gabapentin diazole red 2J validation studies SPhU |
Дата публикации: | 2023 |
Библиографическое описание: | Miedviedieva K. Development and validation of a new spectrophotometric method for the determination of gabapentin in capsules / K. Miedviedieva, S. Vasyuk, O. Portna // ScienceRise: Pharmaceutical Science. - 2023. - N 3. - P. 50-57. - https://doi.org/10.15587/2519-4852.2023.283270. |
Аннотация: | In Ukraine, there are about 100 thousand people with epilepsy. Gabapentin is an effective antiepileptic agent
for oral use, presented in capsules of different dosages from different manufacturers. Therefore, the urgent task
of pharmaceutical analysis today is the development of highly accurate, reliable, affordable and fast methods of
quantitative determination.
The aim of the work is to develop a spectrophotometric technique for the quantitative determination of gabapentin
in capsules based on the reaction with diazole red 2J in compliance with the SPhU.
Material and methods. As reagent and solvent, diazole red 2J of AR grade, acetone of AR grade and purified water
was used. Analytical equipment: Specord 200 and Specord 250 Plus spectrophotometers, ABT-120-5DM and
Radwag XA 210.4Y electronic scales, Elmasonic E 60H and Sonorex Digitec DT100H ultrasonic baths, measuring
glassware of A class.
Results. A simple, accurate and eco-friendly colourimetric method was developed for the quantification of gabapentin
in capsules. The method was based on the reaction of gabapentin with diazole red 2J to give a coloured
product having analytical maxima at 390 nm. Factors affecting colour development and stability were optimized
and incorporated into the procedure. Regression analysis of Beer’s plot showed a good correlation (not less than
0.999) in a concentration range of 2.10–3.64 mg/100 ml. The detection and quantification limits were 2.25 % and
6.19 %, respectively. The intra- and inter-laboratory precision demonstrates and reflects no interference by the
capsule additives and confirms the reproducibility of the method in the selected concentration range. The prediction
of the total uncertainty of the results of the developed method is calculated and displayed to assess the correctness
of the reproduction of the method.
Conclusions. It has been proven that the developed method meets the requirements of the State Pharmacopoeia of
Ukraine and allows to perform the correct quality control of medicinal products |
URI: | http://dspace.zsmu.edu.ua/handle/123456789/19454 |
Располагается в коллекциях: | Наукові праці. (Фармацевтична хімія) Наукові праці. (Аналітична хімія)
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