2012
DOI: 10.4314/tjpr.v11i2.14
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Development of Ultraviolet Spectrophotometric Method for Analysis of Lornoxicam in Solid Dosage Forms

Abstract: Purpose: An ultraviolet spectrophotometric system was developed and validated for the quantitative determination of lornoxicam in solid dosage forms. Methods:Lornoxicam was dissolved in 0.01M NaOH and analysed using ultraviolet (UV) spectrophotometry. Various analytical parameters such as linearity, precision, accuracy, limit of detection (LOD)

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Cited by 6 publications
(4 citation statements)
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“…Using the Student's t-test and the variance ratio F-test, 65 the results obtained were compared to those of reported methods. 22,34,41 According to the calculated t and F values, 65 there is no considerable difference between the methods in terms of accuracy and precision, respectively as shown in Table 5.…”
Section: Structure Versus Activity Correlationmentioning
confidence: 88%
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“…Using the Student's t-test and the variance ratio F-test, 65 the results obtained were compared to those of reported methods. 22,34,41 According to the calculated t and F values, 65 there is no considerable difference between the methods in terms of accuracy and precision, respectively as shown in Table 5.…”
Section: Structure Versus Activity Correlationmentioning
confidence: 88%
“…The accuracy of the proposed method was demonstrated by comparing the results of the proposed method in raw materials and pharmaceuticals to the results of the comparison methods. 22,34,41 Data in Table 3 illustrate no signicant differences between the performance of the two methods concerning the accuracy and precision. This was conrmed by statistical analysis of the data using Student's t-test and variance ratio F-test, respectively.…”
Section: Validation Of the Methodsmentioning
confidence: 98%
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“…The basis for the use of the spectrophotometric method is to determine the wavelength that has been absorbed and to determine the degree of intensity of radiation passing through the tested sample [9]. Spectrophotometric methods are a commonly used method, among others, in the study of biochemical processes (monitoring enzymatic reactions, determination of reaction products, measurement of the reaction rate) [10][11][12][13][14] or for quick monitoring of enzymatic reactions, both for measuring the reaction rate and determining reaction products [15]. Direct analyses are possible only when the wavelength characteristic for the determined component is not disturbed by other components or by background absorption [16,17].…”
Section: Introductionmentioning
confidence: 99%