scholarly journals Determination of the binding constant of imidazole and histidine with immobilized Cu(II) by differential UV spectroscopy.

1995 ◽  
Vol 28 (4) ◽  
pp. 419-424 ◽  
Author(s):  
Ching-Fa Wu ◽  
Wen-Yih Chen ◽  
Hwai-Shen Liu
1990 ◽  
Vol 23 (5) ◽  
pp. 843-861 ◽  
Author(s):  
I. Shoukrallah ◽  
A. Sakla ◽  
R. Wintersteiger

1981 ◽  
Vol 23 (7) ◽  
pp. 1845-1847
Author(s):  
L.V. Morozova ◽  
E.I. Brodskaya ◽  
D.-S.D. Taryashinova ◽  
S.V. Amosova ◽  
B.A. Trofimov

INDIAN DRUGS ◽  
2017 ◽  
Vol 54 (03) ◽  
pp. 44-51
Author(s):  
B. Sabbagh ◽  
B. V. S. Lokesh ◽  
G. A. Akouwah ◽  

Two methods were developed for the determination of dapagliflozin (DAPA) in pure form and in tablets. The procedure utilized was UV-Visible Spectroscopy and RP-HPLC with PDA detector to quantify DAPA in bulk and tablets. The sensitive linear range was identified for both methods within 0.5-5.0μg/mL. The linear regression analysis was identified for both methods with correlation coefficient(r)>0.99. The LOD and LOQ values were found to be 0.05 μg/mL and 0.5 μg/mL for the method by UV-Spectroscopy. The molar absorptivity (ε) was calculated as 1.27 X 105 L.mol-1cm-1. The RP-HPLC method produced LOD and LOQ values of 1.0 ng/mL and 0.5 μg/mL. Both methods were simple, precise, reproducible to quantify the amount of unknown in bulk as well as in tablets and estimated accurately within the range of 100.0±0.5%. Statistical analysis was performed on the data obtained. There was no significant difference between the developed and reported methods with p>0.05. Both methods can be applied for routine analysis of DAPA in bulk and tablets with good accuracy and precision.


2010 ◽  
Author(s):  
S. J. Mohamad-Yob ◽  
M. Ziegler ◽  
T. Rauch ◽  
K. Werner ◽  
Klaus Werner ◽  
...  

2018 ◽  
Vol 11 (06) ◽  
pp. 1850034
Author(s):  
Hongxia Huang ◽  
Yuanyuan Lv ◽  
Xiaoyi Sun ◽  
Shuangshuang Fu ◽  
Xuefang Lou ◽  
...  

A technique for the determination of tannin content in traditional Chinese medicine injections (TCMI) was developed based on ultraviolet (UV) spectroscopy. Chemometrics were used to construct a mathematical model of absorption spectrum and tannin reference content of Danshen and Guanxinning injections, and the model was verified and applied. The results showed that the established UV-based spectral partial least squares regression (PLS) tannin content model performed well with a correlation coefficient ([Formula: see text]) of 0.952, root mean square error of calibration (RMSEC) of 0.476[Formula: see text][Formula: see text]g/ml, root mean square error of validation (RMSEV) of 1.171[Formula: see text][Formula: see text]g/ml, and root mean square error of prediction (RMSEP) of 0.465[Formula: see text][Formula: see text]g/ml. Pattern recognition models using linear discriminant analysis (LDA) and [Formula: see text] nearest neighbor ([Formula: see text]-NN) classifiers based on UV spectrum could successfully classify different types of injections and different manufacturers. The established method to measure tannin content based on UV spectroscopy is simple, rapid and reliable and provides technical support for quality control of tannin in Chinese medicine injections.


Author(s):  
Manas Ranjan Mishra ◽  
Punam Agrawal ◽  
Surya Narayan Das

Capecitabine is a 'pro-drug' to the cytotoxic agent 5-fluorouracil (5-FU) intended to administered orally. Capecitabine is generally used as first line monotherapy for advanced colon cancer. Simple, rapid, accurate UV spectrophotometric methods were developed in the present study and validated for the estimation of Capecitabine in bulk and its formulations as per ICH guidelines. Three solvent systems viz., 0.1N NaOH, 0.1N HCl and Methanol: Water (1:3) was tried. The results suggest that the developed method shows linearity over the range of concentration 2-24μg/ml and a correlation coefficient of 0.9999. Accuracy, precision, linearity, robustness, and ruggedness were statistically validated as per ICH guidelines for all the developed methods. The % RSD values for validated methods were found to be less than 1.5 and methods will find application in routine analysis of drug formulations containing Capecitabine.


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