New flow injection method for quality control of dietary supplements containing l-carnitine using extraction mediated by sodium taurodeoxycholate coacervate coupled to molecular fluorescence

2016 ◽  
Vol 129 ◽  
pp. 268-273 ◽  
Author(s):  
Andrea C. Isaguirre ◽  
Gimena Acosta ◽  
Soledad Cerutti ◽  
Liliana P. Fernandez





2000 ◽  
Vol 49 (1) ◽  
pp. 59-64 ◽  
Author(s):  
Hiroki OHURA ◽  
Toshihiko IMATO ◽  
Ikuo MATSUO ◽  
Sumio YAMASAKI


1991 ◽  
Vol 24 (4) ◽  
pp. 581-588 ◽  
Author(s):  
M. Yaqoob ◽  
M. Anwar ◽  
A. S. Masood ◽  
M. Masoom


Author(s):  
Dieu Thu Nguyen Thi ◽  
Dung Hoang Viet ◽  
Hong Ngoc Nguyen Thi ◽  
Thanh An Vu Thi ◽  
Thanh Hoa Mac Thi ◽  
...  

Nattokinase is an enzyme with a strong fibrinolytic activity that can be used for preventing thrombolytic diseases. The fibrinolytic activity of the Nattokinase in dietary supplements is determined by spectrophotometric method. In this study, the conditions of the assay were examined and finally optimized as pH: 8.5, reaction temperature: 40oC, and reaction time: 60 minutes. The proposed method was validated and successfully applied to determine the Nattokinase activity in 10 dietary supplements. The results showed that the proportion of measured activity compared to label product activity were within in the range 79.1 - 98.0%. The effect of herbal compounds and excipients on Nattokinase activity were also surveyed. From the evaluated results and application to commercial samples, this method will be a valuable contribution to quality control of dietary supplement products containing Nattokinase.  



2018 ◽  
Vol 33 (2) ◽  
pp. 47
Author(s):  
Orlando Fatibello-Filho ◽  
Heberth Juliano Vieira

A spectrophotometric flow injection method for the determination of paracetamol in pharmaceutical formulations is proposed. The procedure was based on the oxidation of paracetamol by sodium hypochloride and the determination of the excess of this oxidant using o-tolidine dichloride as chromogenic reagent at 430 nm. The analytical curve was linear in the paracetamol concentration range from 8.50 x 10-6 to 2.51 x 10-4 mol L-1 with a detection limit of 5.0 x 10-6 mol L-1. The relative standard deviation was smaller than 1.2% for 1.20 x 10-4 mol L-1 paracetamol solution (n = 10). The results obtained for paracetamol in pharmaceutical formulations using the proposed flow injection method and those obtained using a USP Pharmacopoeia method are in agreement at the 95% confidence level.



Talanta ◽  
2021 ◽  
pp. 123161
Author(s):  
Missael Antonio Arroyo Negrete ◽  
Kazimierz Wrobel ◽  
Eunice Yanez Barrientos ◽  
Alma Rosa Corrales Escobosa ◽  
Israel Enciso Donis ◽  
...  




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