Method Transfer Evaluation for Digital Derivative Spectrophotometry Through its Resolution Parameter Comparison of Different Computer Programs

2020 ◽  
Vol 74 (5) ◽  
pp. 525-535
Author(s):  
Ana Homšek ◽  
Bojan Marković ◽  
Nataša Bogavac-Stanojević ◽  
Sote Vladimirov ◽  
Katarina Karljiković-Rajić

The application assessment of different programs was performed with equivalence tests for method transfer pro second-order derivative spectrophotometry. The digital second-order derivative spectra were calculated on different instruments; GBC Scientific Equipment Cintra 20 (Cintral v.2.6 and Spectral v.1.70 software programs) and Thermo Scientific Evolution 300 (VISIONPro software) were analyzed using the amplitude A/B ratio (A = 2D265,263; B = 2D263,261). Amplitude A/B ratio is the resolution parameter for derivative spectrophotometry prescribed in European Pharmacopoeia. The obtained values for A/B ratio were either very similar or significantly different among programs: 0.669 (Cintral v.2.6), 0.549 (Spectral v.1.70), 0.556 (medium indirect VISIONPro), 0.557 (one-step Savitzky–Golay 7 VISIONPro), 0.689 (two-step Savitzky–Golay 7 VISIONPro). Method transfer was possible between Spectral v.1.70 and VISIONPro (medium indirect and one-step Savitzky–Golay 7), but the values obtained in Cintral v.2.6 were not comparable to the other programs. The absorbance data exported from both instruments were additionally calculated in OriginPro8 which provided almost the same mean A/B values (0.627 Cintral v.2.6; 0.624 VISIONPro), confirming that the two instruments recorded the same zero-order spectra. The calculation of resolution parameter could be used for verification of program comparison, which would enable transfer between sender and receiver laboratory. The accordance between program algorithms was confirmed when acceptable differences for values of resolution parameter (A/B ratios) were achieved.

2014 ◽  
Vol 64 (4) ◽  
pp. 433-446 ◽  
Author(s):  
Mohamed M. Hefnawy ◽  
Mostafa S. Mohamed ◽  
Mohammed A. Abounassif ◽  
Amer M. Alanazi ◽  
Gamal A. E. Mostafa

Abstract High performance liquid chromatography (HPLC) and second-order derivative spectrophotometry have been used for simultaneous determination of pravastatin (PS) and fenofibrate (FF) in pharmaceutical formulations. HPLC separation was performed on a phenyl HYPERSIL C18 column (125 mm × 4.6 mm i.d., 5 μm particle diameter) in the isocratic mode using a mobile phase acetonitrile/0.1 % diethyl amine (50:50, V/V, pH 4.5) pumped at a flow rate of 1.0 mL min-1. Measurement was made at 240 nm. Both drugs were well resolved on the stationary phase, with retention times of 2.15 and 5.79 min for PS and FF, respectively. Calibration curves were linear (R = 0.999 for PS and 0.996 for FF) in the concentration range of 5-50 and 20-200 µg mL-1 for PS and FF, respectively. Pravastatin and fenofibrate were quantitated in combined preparations also using the second-order derivative response at 237.6 and 295.1 nm for PS and FF, respectively. Calibration curves were linear, with the correlation coefficient R = 0.999 for pravastatin and fenofibrate, in the concentration range of 5-20 and 3-20 µg mL-1 for PS and FF, respectively. Both methods were fully validated and compared, the results confirmed that they were highly suitable for their intended purpose.


2014 ◽  
Vol 14 (5) ◽  
pp. 389-390
Author(s):  
Yan HAN ◽  
ZhiLiang YU ◽  
Jun WEN ◽  
TingTing ZHOU ◽  
ChunQuan SHENG ◽  
...  

2009 ◽  
Vol 42 (1) ◽  
pp. 84-93 ◽  
Author(s):  
A. Praveen Kumar ◽  
P. Raveendra Reddy ◽  
V. Krishna Reddy ◽  
Y. I. Lee

1996 ◽  
Vol 12 (3) ◽  
pp. 427-430 ◽  
Author(s):  
Toshiaki HIYAMA ◽  
Shinichi SUGAYA ◽  
Tomio KAGEYAMA ◽  
Katsuichiro KAMIMURA

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