Solubility Determination of Nitazoxanide in Twelve Organic Solvents from T = 273.15 to 313.15 K

2020 ◽  
Vol 65 (7) ◽  
pp. 3645-3651
Author(s):  
Haojian Zhang ◽  
Yuli Shi ◽  
Haoji Wang
1966 ◽  
Vol 12 (4) ◽  
pp. 206-210 ◽  
Author(s):  
Royce D Stauffer ◽  
Fritz Bischoff

Abstract In a study of the solubility of crystalline forms of cholesterol in various solvents, the solubilities (per cent by weight) of cholesterol needles and hydrated plates at 38° were, respectively, 4.0 and 3.2% in olive oil; 2.6 and 1.9% in tetradecane; 26.2 and 9% in toluene; and 21.0 and 7% in cyclohexane. When these solvents are in equilibrium with an aqueous phase, needles are converted to plates. Pseudomorph ( dehydrated) plates in olive oil have the solubility of needles. These differences may have significance in studies involving cholesterol pathogenesis. The modified Zak reaction with ethanol could not be used for the assay of cholesterol in olive oil since the reaction product was turbid. Higher alcohols were studied as a substitute for ethanol; 2-propanol was satisfactory.


1960 ◽  
Vol XXXV (I) ◽  
pp. 34-48 ◽  
Author(s):  
Gerd Ittrich

ABSTRACT A series of organic solvents and phenol derivatives have been examined for the extraction of the pink Kober-colour complex. Optimal results could be achieved for fluorimetry by a solution of 2 % (w/v) p-nitrophenol and 1 % (v/v) ethanol in acetylenetetrabromide, when the green mercury line (546 mμ was used as primary light. The sensitivity, stability and specificity have been improved, compared with the previously described reaction. By changing the sequence of purification steps and by reducing the volume of the urine sample (5 ml) the method for the determination of total oestrogens has been simplified. Approximately 10 determinations can be done within 3–4 hours by one person. Recovery experiments and comparative determinations with a previously described method have been carried out. The excretion of total oestrogens in a complete menstrual cycle is determined with the described method.


2014 ◽  
Vol 32 (11) ◽  
pp. 1251
Author(s):  
Jing DA ◽  
Xianglu HUANG ◽  
Gangli WANG ◽  
Jin CAO ◽  
Qingsheng ZHANG

2016 ◽  
Vol 99 (6) ◽  
pp. 1533-1536 ◽  
Author(s):  
Jéssica Sayuri Hisano Natori ◽  
Eliane Gandolpho Tótoli ◽  
Hérida Regina Nunes Salgado

Abstract Norfloxacin is a broad-spectrum antimicrobial agent, widely used in humans and animals for the treatment of urinary tract infections. It is a second-generation fluoroquinolone. Several analytical methods to analyze norfloxacin have been described in the literature. However, most of them are complex and require the use of large amounts of organic solvents. This paper describes the development and validation of a green analytical method for the determination of norfloxacin in raw material by FTIR spectrophotometry. This method does not require the use of organic solvents, minimizing waste generation in the process and its environmental impacts. The development of methods that promote the reduction, prevention, or elimination of waste generation has become highly attractive to the pharmaceutical industry because of the growing demand from civil society and government authorities for environmentally friendly products and services. The FTIR spectrophotometry method was validated according to International Conference on Harmonization guidelines, showing adequate linearity (r = 0.9936), precision, accuracy, and robustness. This validated method can be used as an environmentally friendly alternative for the quantification of norfloxacin in raw material in QC routine analysis.


2018 ◽  
Vol 67 (8) ◽  
pp. 461-468
Author(s):  
Takahisa YAMAMOTO ◽  
Seiichi SUZUKI ◽  
Mami OZAWA ◽  
Yasuyuki KOBAYASHI ◽  
Yoshinori INOUE

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