scholarly journals Three smart spectrophotometric methods for resolution of severely overlapped binary mixture of Ibuprofen and Paracetamol in pharmaceutical dosage form

BMC Chemistry ◽  
2019 ◽  
Vol 13 (1) ◽  
Author(s):  
Christine M. El-Maraghy ◽  
Nesrine T. Lamie
Author(s):  
Pushpa Latha E. ◽  
Sailaja B.

Analytical UV derivative spectrophotometric method was developed and validated to quantify Rizatriptan Benzoate in pure drug and tablet dosage form. Based on the spectrophotometric characteristics of Rizatriptan Benzoate, a signal of zero (225nm), first (216nm), second (237nm), third (233nm), fourth (231nm) order derivative spectra were found to be adequate for quantification. The methods obeyed Beer's law in the concentration range of (0.1-360µg/ml) with square correlation coefficient (r2) of 0.999. The mean percentage recovery was found to be 100.01 ± 0.075. As per ICH guidelines the results of the analysis were validated in terms of linearity, precision, accuracy, limit of detection and limit of quantification, and were found to be satisfactory.


2017 ◽  
Vol 7 (1) ◽  
pp. 30-42 ◽  
Author(s):  
Hayam Mahmoud Lotfy ◽  
Yasmin Mohammed Fayez ◽  
Shereen Mostafa Tawakkol ◽  
Nesma Mahmoud Fahmy ◽  
Mostafa Abd El-Atty Shehata

2015 ◽  
Vol 7 (13) ◽  
pp. 5674-5681 ◽  
Author(s):  
M. Sharaf El-Din ◽  
M. Eid ◽  
Abdallah M. Zeid

Two simple and rapid spectrophotometric methods for the simultaneous determination of methocarbamol and aspirin in their combined dosage form.


2009 ◽  
Vol 6 (2) ◽  
pp. 537-540 ◽  
Author(s):  
Manish Majumder ◽  
B. Gopinath ◽  
Girish Koni ◽  
Sanjeev Kumar Singh

Two new, selective and sensitive visible spectrophotometric methods (method A and B) have been developed for the estimation of tinofovir in bulk and in pharmaceutical preparations. Tinofovir was subjected to acid hydrolysis and this acid hydrolyzed drug was used for the estimation. Method A is based on the reaction with 3-methyl-2-benzothiazolinone hydrazone in the presence of ferric chloride, to form a colored species with a λmaxat 628.5 nm. Method B is based on the reaction with Folin-ciocalteu phenol’s reagent under alkaline condition with a λmaxat 768 nm. Beer’s law is obeyed in the concentration range of 5-40 µg/mL for method A and 2-30 µg/mL for method B, respectively. The methods were extended to pharmaceutical formulations and there was no interference from any common pharmaceutical excepients and diluents. The result of analysis has been validated statistically and by recovery studies.


2019 ◽  
Vol 65 (2) ◽  
pp. 55-59 ◽  
Author(s):  
Béla Kovács ◽  
Réka Molnár ◽  
Előd Ernő Nagy ◽  
Éva Katalin Kelemen ◽  
Blanka Székely-Szentmiklósi ◽  
...  

AbstractObjective: The present work offers a fast, reliable and easy UV spectrophotometric method for the assay of strontium ranelate from bulk samples and pharmaceutical dosage form.Methods: The proposed method uses 0.1% V/V trichloroacetic acid as dissolution medium for spectrophotometric analysis, by signal detection at 321 nm. The method was validated according to the currently in-force international guidelines for linearity, accuracy, precision, robustness, limit of detection and quantification.Results: The method was found to be linear in the range of 5-100 µg mL-1 (R2 > 0.999). Method accuracy was found in-between 98.87-100.41%, showing good linear correlation as well (R2 = 0.9997). The concentrations for limit of detection and limit of quantitation were found 1.13 µg mL-1 and 3.77 µg mL-1, resp. The proposed method showed good intra- and interday precision, with low RSD values of 0.53-1.24% and 1.11%, resp.Conclusions: Stability studies performed by both HPLC and UV spectrophotometric methods revealed that the active substance is highly susceptible to acidic hydrolysis, oxidation and exposure to high temperature.


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