scholarly journals Application of steam carrier gas chromatography to analyses of pharmaceuticals; I. Determination of salicylic acid and phenol in pharmaceutical preparations in the Japanese Pharmacopoeia X.

1986 ◽  
Vol 35 (3) ◽  
pp. 193-197 ◽  
Author(s):  
Muneo MORISHITA ◽  
Hideaki IIZUKA ◽  
Masa KATAYANAGI ◽  
Takehiko YAJIMA
2001 ◽  
Vol 84 (3) ◽  
pp. 676-683 ◽  
Author(s):  
Natividad Ramos-Martos ◽  
Francisco Aguirre-Gómez ◽  
Antonio Molina-Díaz ◽  
Luis F Capitán-Vallvey

Abstract This paper describes a rapid reversed-phase liquid chromatographic method, with UV detection, for the simultaneous determination of acetylsalicylic acid, caffeine, codeine, paracetamol, pyridoxine, and thiamine in pharmaceutical preparations. A reversed-phase C18 Nucleosil column is used. The mobile phase consists of 2 successive eluants: water (5 min) and acetonitrile–water (75 + 25, v/v; 9 min), both adjusted to pH 2.1 with phosphoric acid. Before determination acetylsalicylic acid is completely converted to salicylic acid by alkaline hydrolysis. Salicylic acid, caffeine, paracetamol, pyridoxine, and thiamine are all detected at 285 nm, whereas codeine is detected at 240 nm. Calibration curves were linear for salicylic acid, caffeine, paracetamol, and pyridoxine in the range of 50–500 mg/L, and for codeine and thiamine in the range of 50–1000 mg/L. The method was applied to the analysis of 13 fortified commercial pharmaceutical preparations. Recoveries ranged from 92.6 to 105.5%, with relative standard deviations of 1.1–5.8%.


1990 ◽  
Vol 12 (6) ◽  
pp. 263-266 ◽  
Author(s):  
J. M. López Fernández ◽  
M. D. Luque de Castro ◽  
M. Valcárcel

An asymmetrical FIA merging-zones manifold based on the dual injection of two sample microvolumes was developed for the simultaneous determination of salicylic acid and acetylsalicylic acid in pharmaceutical preparations at a sampling frequency of 30/h. The complex formed between the Fe(III) reagent continuously introduced in the system and salicylic acid was monitored photometrically at 520 nm. One of the sample plugs was prehydrolysed on injection into an NaOH stream and was circulated through a longer channel than the other plug. This yielded two FIA peaks corresponding to salicylic acid and the overall content, respectively. The proposed manifold was successfully used to control the dissolution test of a pharmaceutical preparation.


1964 ◽  
Vol 47 (4) ◽  
pp. 730-734
Author(s):  
Howard L Ashmead ◽  
Glenn E Martin ◽  
John A Schmit

Abstract A fast and direct method is presented for the determination of CO2 in wines. Partial pressures from other ingredients of alcoholic beverages do not interfere. The method was compared to the manometric procedure under vacuum. An F & M Model 450 Gas Chromatograph with a filament detector was used for C02 determinations. Components were separated by a column 9” long and 1/8” o.d. using charcoal (60—80 mesh) as solid adsorbent. Injection port temperature was ambient; detector and column temperatures were 40°C. Helium was used as a carrier gas at the rate of 50 ml/min. Approximately 50 μ1 samples of standard and unknown solutions were used for the respective determinations.


1995 ◽  
Vol 9 (3) ◽  
pp. 155-156 ◽  
Author(s):  
Yun-Hua Li ◽  
Zi-Hong Ren ◽  
Xiu-Lu Li ◽  
Yi-Feng Cai ◽  
Zheng-Xing Zhai
Keyword(s):  

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