Artem Myhal; Anna Dobrova; Olga Golovchenko; Victoriya Georgiyants
Authors place of work:
The National University of Pharmacy, Kharkiv, Ukraine
Published in the journal:
Čes. slov. Farm., 2015; 64, 225-227
44<sup>th</sup> Conference drug synthesis and analysis
The international community imposes stringent requirements for the quality and safety of products. Nevertheless, counterfeiting of medicines is a special social danger and an urgent problem. Therefore, the suggested methods of quality control must comply with regulatory requirements and fully confirm the quality of goods.
Validation of quality control methods is recommended by the State Pharmacopoeia of Ukraine (SPhU) and the world’s leading Pharmacopoeias during the registration of medicines. This procedure aims to experimentally verify the correctness and accuracy of the above methods1–3, 6, 7, 10–13).
The guarantee of the safety and effectiveness of drugs is also their stability and absence of side effects of interaction that can take place in the organism, with different active ingredients. This applies to simultaneously appointed drugs and components of food, drinks, mineral water, food additives that people use independently in their daily diet. Patients rarely adhere to the recommended diet, without changing their eating habits. Therefore, the study of influence of the most common cases of interaction on bioavailability and pharmacological activity of prescribed drugs is relevant.
In order to experimentally prove the expediency or inadmissibility of the combined use of metronidazole as a helicobacter drug with others drugs, food, mineral water and other beverages rich in metal cations, we carried out validation of analytical method of assaying metronidazole in capsules by the standard method within the UV-spectrophotometric method according to the SPhU requirements, which is planned for use in studying the bioavailability of products of metronidazole interaction with metal salts.
The object of study is metronidazole capsules “TRIKACIDE” with the content of the active substance constituting 500 mg (manufactured by PHARMASCIENCE INC., Quebec, Canada, Series: 6452653).
The standard sample substance of metronidazole (manufactured by LUOTIAN HONGYUAN BIOCHEMICAL CO., LTD, China Series: 08111803) was used to prepare the metronidazole reference solution.
An “Evolution 60S” Spectrophotometer (USA), a “Specord 200” Spectrophotometer (Germany), a AB 204 S/A METTLER TOLEDO analytical balance as well as a class A measuring vessel and reagents that conform to the SPhU were used in the study.
Methods of assaying metronidazole in capsules
The exact weight amount of the contents of 20 capsules, equivalent to 0.1000 g of metronidazole (approximately 0.1209 g) is placed in a 100.0 ml volumetric flask, 50 ml of 0.1 M hydrochloric acid solution is added, shaken for 15 minutes, brought to the mark with the same solvent. The obtained solution is then filtered, the first and the last portions of the filtrate are rejected. The aliquot of 1.0 ml of the resulting solution is taken and placed in a 100.0 ml volumetric flask and adjusted to the mark with the same solvent. The measurement of absorbance is carried out on a spectrophotometer at 277 nm wavelength in a ditch with a layer thickness of 10 mm. The measurement of the metronidazole standard sample solution absorbance was carried out at the same time10–13).
Compensation solution is 0.1 M hydrochloric acid solution.
The content of the active ingredient, according to the SPhU should be between 90–110% of the nominal content per average weight of the capsules contents (0.450–0.550)13).
Linearity, accuracy, precision and reproducibility were studied in model mixtures of a series of samples containing the known amounts of active substances and excipients. The study was conducted in the application range of 80–120% method with 5% increments. Absorbance was measured three times with the cell removed. The average value was used for the results calculation 1–6, 8–9, 14).
Results and discussion
The graph (Figure 1) confirms the linear dependence of absorbance on the concentration of the metronidazole solution1,4, 5, 12).
The calculation of the linear dependence for metronidazole was performed by the least squares method (Table 1).
According to Table 1, the parameters of linear dependence correspond to the requirements, confirming the linearity of the proposed methods.
The criterion of practical uncertainty of methods for systematic error was 0.66%, executed at γ, % = 0.66 ≤ 1.024, characterizing the accuracy of the proposed spectrophotometric method of assaying in the range of applying the 80–120% method.
This method is characterized by convergence, as the relative confidence interval, ΔZ, % = t(95%,8) · Sz = 1.0957 is below the critical value for convergence of results, which is in this case 3.20% (Table 2).
The research of reproducibility is anecessary condition if the method is planned to be included to the pharmacopeia and to be transferred to another laboratory. This parameter characterizes the accuracy of interlaboratory study methods on aseries of test solutions1–2, 4, 5, 12, 15). The reproducibility was studied by measuring the optical absorption of the series of analytical solutions in different laboratories, with different equipment, by different analysts.
The data show that the proposed method can be correctly reproduced in other laboratories and characterized by the relative confidence interval of 100 ± 0.58% with aprobability of 95%. Value Δx,r, % = 0.58 ≤ 3,2. The interlaboratory systematic error constituted 0.54%.
The projected total uncertainty of results of assaying methods ΔAS is 1.16% and not greater than the critical value (3.20%), which is insignificant.
The data confirm that the solutions are stable during the research time. The stability of solutions confirms an insignificant impact of reagents, equipment, and the subjective factor if the method is transferred.
To assess the “robustness“, the stability of the test solutions was studied by measuring their absorbance every 15 minutes during an hour 1, 4–6) (Table 3).
Validation characteristics for the proposed assaying method were defined. Eligibility criteria for content tolerances of ± 10% were used.
The researched validation characteristics confirm linearity, precision (convergence, reproducibility), as well as the accuracy of the proposed method.
The prediction of total uncertainty of the proposed methods, determined with the use of the methods transferred, meets the eligibility criteria, which confirms the possibility of using the method of assaying the metronidazole capsules in other laboratories.
Conflicts of interest: none.
The National University of Pharmacy
53, Pushkinska str., 61002 Kharkiv, Ukraine
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