{"title":"紫外分光光度法同时测定混悬液中布洛芬和扑热息痛的浓度","authors":"E. Mugwiza, I. Hahirwa, T. Umumararungu","doi":"10.4314/rmj.v80i3.7","DOIUrl":null,"url":null,"abstract":"
 
 
 INTRODUCTION: Paracetamol is a standard antipyretic and analgesic which is widely used since the 19th century. Currently, paracetamol is the first-line treatment for pain management of different types. Ibuprofen, on the other hand, is an antipyretic and an analgesic. It is safe and has been used in the treatment of a number of conditions including mild to moderate pain, dysmenorrhea, inflammations and fever to name few.
 METHODS: This study aimed at developing and validating a simultaneous UV spectrophotometric method for analysis of ibuprofen and paracetamol in fixed-dose combination suspensions. The proposed method is based on the simultaneous equation principle, which involves measurement of absorbance at wavelengths of maximum absorbance for ibuprofen and paracetamol. The method was validated for linearity, accuracy, repeatability, intermediate precision and robustness as per USP and ICH guidelines.
 RESULTS: The two molecules showed wavelength of maximum absorbance at 222 nm and 243 nm for ibuprofen and paracetamol respectively, using phosphate buffer as a diluent. The method was also linear (R2≥0.995), precise (RSD ≤ 2), and robust with accuracy ranging between 98.1%-105% and 109.8 %- 134.9% for paracetamol and ibuprofen, in the range of 0.0032 – 0.0048 mg/ml for ibuprofen and 0.004-0.006 mg/ml for paracetamol, respectively.
 CONCLUSION: We have developed an accurate and robust method which can be used to analyze quantitatively paracetamol in suspensions which contain both paracetamol and ibuprofen. The limits of quantification of this method cover the concentration range recommended by the USP (80%- 120%), which justifies the application of the method in routine analysis.
 
 
","PeriodicalId":38181,"journal":{"name":"Rwanda Medical Journal","volume":"126 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A UV Spectrophotometric method for simultaneous determination of Ibuprofen and Paracetamol concentration in suspensions\",\"authors\":\"E. Mugwiza, I. Hahirwa, T. Umumararungu\",\"doi\":\"10.4314/rmj.v80i3.7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"
 
 
 INTRODUCTION: Paracetamol is a standard antipyretic and analgesic which is widely used since the 19th century. Currently, paracetamol is the first-line treatment for pain management of different types. Ibuprofen, on the other hand, is an antipyretic and an analgesic. It is safe and has been used in the treatment of a number of conditions including mild to moderate pain, dysmenorrhea, inflammations and fever to name few.
 METHODS: This study aimed at developing and validating a simultaneous UV spectrophotometric method for analysis of ibuprofen and paracetamol in fixed-dose combination suspensions. The proposed method is based on the simultaneous equation principle, which involves measurement of absorbance at wavelengths of maximum absorbance for ibuprofen and paracetamol. The method was validated for linearity, accuracy, repeatability, intermediate precision and robustness as per USP and ICH guidelines.
 RESULTS: The two molecules showed wavelength of maximum absorbance at 222 nm and 243 nm for ibuprofen and paracetamol respectively, using phosphate buffer as a diluent. The method was also linear (R2≥0.995), precise (RSD ≤ 2), and robust with accuracy ranging between 98.1%-105% and 109.8 %- 134.9% for paracetamol and ibuprofen, in the range of 0.0032 – 0.0048 mg/ml for ibuprofen and 0.004-0.006 mg/ml for paracetamol, respectively.
 CONCLUSION: We have developed an accurate and robust method which can be used to analyze quantitatively paracetamol in suspensions which contain both paracetamol and ibuprofen. The limits of quantification of this method cover the concentration range recommended by the USP (80%- 120%), which justifies the application of the method in routine analysis.
 
 
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A UV Spectrophotometric method for simultaneous determination of Ibuprofen and Paracetamol concentration in suspensions
INTRODUCTION: Paracetamol is a standard antipyretic and analgesic which is widely used since the 19th century. Currently, paracetamol is the first-line treatment for pain management of different types. Ibuprofen, on the other hand, is an antipyretic and an analgesic. It is safe and has been used in the treatment of a number of conditions including mild to moderate pain, dysmenorrhea, inflammations and fever to name few.
METHODS: This study aimed at developing and validating a simultaneous UV spectrophotometric method for analysis of ibuprofen and paracetamol in fixed-dose combination suspensions. The proposed method is based on the simultaneous equation principle, which involves measurement of absorbance at wavelengths of maximum absorbance for ibuprofen and paracetamol. The method was validated for linearity, accuracy, repeatability, intermediate precision and robustness as per USP and ICH guidelines.
RESULTS: The two molecules showed wavelength of maximum absorbance at 222 nm and 243 nm for ibuprofen and paracetamol respectively, using phosphate buffer as a diluent. The method was also linear (R2≥0.995), precise (RSD ≤ 2), and robust with accuracy ranging between 98.1%-105% and 109.8 %- 134.9% for paracetamol and ibuprofen, in the range of 0.0032 – 0.0048 mg/ml for ibuprofen and 0.004-0.006 mg/ml for paracetamol, respectively.
CONCLUSION: We have developed an accurate and robust method which can be used to analyze quantitatively paracetamol in suspensions which contain both paracetamol and ibuprofen. The limits of quantification of this method cover the concentration range recommended by the USP (80%- 120%), which justifies the application of the method in routine analysis.
期刊介绍:
The Rwanda Medical Journal (RMJ), is a Not-For-Profit scientific, medical, journal that is published entirely online in open-access electronic format. The RMJ is an interdisciplinary research journal for publication of original work in all the major health disciplines. Through a rigorous process of evaluation and peer review, The RMJ strives to publish original works of high quality for a diverse audience of healthcare professionals. The Journal seeks to deepen knowledge and advance scientific discovery to improve the quality of care of patients in Rwanda and internationally.