Spectrophotometric Determination of 6-Mercaptopurine in Pharmaceutical Sample Using Fe(III)-Potassium Ferricyanide System

2014 ◽  
Vol 881-883 ◽  
pp. 479-483 ◽  
Author(s):  
Chang Qing Tu ◽  
Xin Rong Wen

In the present work,we developed a simple,fast,sensitive and inexpensive method to determine 6-mercaptopurine (6-MP) in pharmaceutical sample using Fe (III)-potassium ferricyanide system by spectrophotometry.The results show that in acid medium, Fe (Ш) can be reduced to Fe (II) by hydrosulfuryl (-SH) in 6-Mercaptopurin molecule, and then Fe (II) reacts with potassium ferricyanide to form a soluble Prussian blue (KFeIII[FeII(CN)6]),the content of 6-MP was determinated indirectly through determinating the absorbance of the soluble Prussian blue.The various effect factors on the determination of 6-MP by spectrophotometry using potassium Fe (III)-ferricyanide system were investigated in detail.The maximum absorption wavelength of chromogenic system was 755 nm, good linear relationship was obtained between the absorbance and the concentration of 6-MP in the range of 0.4120~2.884 μ g·/mL,the equation of the linear regression was A=0.0411+0.1462C (μ g·/mL),with a linear correlation coefficient was 0.9991.This proposed method had been successfully applied to determinate of 6-MP in real pharmaceutical,and the results agreed well with those obtained by pharmacopoeial method.

2014 ◽  
Vol 1033-1034 ◽  
pp. 548-551
Author(s):  
Xin Rong Wen ◽  
Chang Qing Tu

A novel method for the spectrophotometric determination of isoniazid by silicomoly- bdenum blue has been established.The various effect factors on the spectrophotometric determination of isoniazid by silicomolybdenum blue were investigated in detail.The results showed that under certain reaction conditions,silicomolybdenum yellow could be reduced to silicomolybdenum blue by isoniazid, and the content of isoniazid was determinated indirectly through determinating the absorbance of the silicomolybdenum blue. The maximum absorption wavelength of chromogenic system is 740 nm, good linear relationship is obtained between the absorbance and the concentration of isoniazid in the range of 1.968~27.55 μg/mL,and the equation of the linear regression is A=0.0247+61.824ρ (μg/mL) with a linear correlation coefficient is 0.9995.This proposed method has been successfully applied to determinate of isoniazid in isoniazid tablets, and the results agree well with those obtained by pharmacopoeial method.


2013 ◽  
Vol 781-784 ◽  
pp. 115-119 ◽  
Author(s):  
Chang Qing Tu ◽  
Xin Rong Wen

A novel method for the indirect determination of methimazole by discoloration spectrophotometry using Fe (Ш)-tiron system has been established.The various effect factors on the determination of methimazole by discoloration spectrophotometry using tiron-Fe (Ш) system were investigated in detail. The results showed that by controlling pH=2.8,Fe (Ш) could be reduced to Fe (II) by hydrosulfuryl (-SH) in methimazole molecule,and then using tiron as chromogenic reagent of Fe (Ш),and the content of methimazole was determinated indirectly through determinating the surplus content of Fe (Ш) in the system.The maximum absorption wavelength of chromogenic system was 663 nm, good linear relationship was obtained between A and the concentration of methimazole in the range of 3.2~12.8μg·mL-1,the equation of the linear regression was A=-0.1849+57.277ρ (mg·mL-1),with a linear correlation coefficient was 0.9998.This proposed method had been successfully applied to determinate of methimazole in real pharmaceutical.


2013 ◽  
Vol 634-638 ◽  
pp. 101-105 ◽  
Author(s):  
Xin Rong Wen ◽  
Chang Qing Tu

A novel method for the indirect determination of methimazole by spectrophotometry using phenanthroline-Fe(Ⅱ) has been established.The results showed that in acid medium, Fe(Ш) could be reduced to Fe(Ⅱ) by hydrosulfuryl(-SH) in methimazole molecule,and then using phenanthroline as chromogenic reagent of Fe(Ⅱ), and the content of methimazole was determinated indirectly through determinating the content of Fe(Ⅱ) by spectrophotometry. The various effect factors on the determination of methimazole by spectrophotometry using phenanthroline-Fe(Ⅱ) were investigated in detail.The maximum absorption wavelength of chromogenic system was 509 nm, good linear relationship was obtained between the absorbance and the concentration of methimazole in the range of 0.0016~0.0064 mg/mL,the equation of the linear regression was A = 0.1942 + 64.598ρ (mg•mL-1),with a linear correlation coefficient was 0.9995.This proposed method had been applied to determinate of methimazole in real pharmaceutical,and the results agreed well with those obtained by pharmacopoeial method.


2021 ◽  
Vol 290 ◽  
pp. 01028
Author(s):  
Changqing Tu ◽  
Xinrong Wen

In acidic media, Fe(Ш) could be reduced to Fe(Ⅱ) by isoniazid, Fe(Ⅱ) reacts with 2,2'-bipyridine to form an orange complex with a maximum absorption wavelength of 522 nm. According to this principle, the content of isoniazid can be measured indirectly by measuring the amount of Fe(Ⅱ). A new method for the determination of isoniazid by Fe(Ⅱ)-2,2'-bipyridine spectrophotometry has been established. At the optimum conditions, the linear relationship is good between the mass concentration of isoniazid and absorbance of Fe(Ⅱ)-2,2'-bipyridine complex in the range of 0.0004000-0.002800 mg/mL. The linear regression equation is A=0.0251+138.04C(mg/mL), and the linear correlation coefficient is 0.9995. This method is used to determine the content of isoniazid in isoniazid tablets, and the results are similar to those obtained by pharmacopoeia method.


2018 ◽  
Vol 53 ◽  
pp. 01046
Author(s):  
Xinrong Wen ◽  
Changqing Tu

Under optimum reaction conditions, Ammonium silicomolybdate could be quantitatively reduced to silicomolybdenum blue by hydrosulfuryl(-SH) in methimazole molecule, and the content of methimazole was determinated indirectly through determinating the absorbance of the silicomolybdenum blue. A novel method for the spectrophotometric determination of methimazole by silicomolybdenum blue has been established. The results showed that the maximum absorption wavelength of silicomolybdenum blue is 730 nm, good linear relationship is obtained between the absorbance of silicomolybdenum blue and the concentration of methimazole in the range of 8.000-160.0μg/mL, and the equation of the linear regression is A=0.0757+11.547ρ (mg/mL) with a linear correlation coefficient is 0.9998. This proposed method has been applied to determinate of methimazole in tablets, and the results agree well with those obtained by pharmacopoeial method.


2021 ◽  
Vol 245 ◽  
pp. 03023
Author(s):  
Changqing Tu ◽  
Xinrong Wen

In the alkaline medium of pH=9.18, Cu2+ can be reduced to Cu+ by the sulfhydryl (-SH) of cysteine, and it result in the decrease the amount of Cu2+ in the system. The decrement of Cu2+ is directly proportional to the addition of cysteine, then using bis-cyclohexanone oxalyldihydrazone (BCO) as chromogenic reagent for Cu2+ to determinate the content of cysteine indirectly by discoloration spectrophotometry. A new method for the determination of cysteine by discoloration spectrophotometry using Copper(II)-BCO has been established. The influencing factors of the determination of cysteine is investigated. The results show that the maximum absorption wavelength of chromogenic system was 602 nm, in the range of 0.008000~0.06800 mg/mL, the linear relationship between the decrease of absorbance and the mass concentration of methimazol is A=0.2162+2.4824C (mg/mL), and the linear correlation coefficient is r=0.9959. The method has been applied to the determination of cysteine in food, and the results are basically consistent with those determined by pharmacopoeial method.


Author(s):  
Pratheema Philomindoss

Objective: The present study is designed to develop a new simple, precise, rapid and selective high‐performance thin‐layer chromatographic (HPTLC) method for the determination of stigmasterol in methanolic rhizomes extract of Alpinia calcarata.Methods: As per International Conference on Harmonization (ICH) guidelines we have applied different concentrations of stigmasterol as standard on HPTLC plates for the quantification of stigmasterol from the Alpinia calcarata rhizomes. The concentration of standard stigmasterol is 1 mg/ml.Results: The retention factor of stigmasterol was 0.58. Linearity was obtained in the range of 50 ng‐250 ng for stigmasterol. The developed and validated HPTLC method was employed for stigmasterol in methanolic rhizomes extract of Alpinia calcarata for standardization of the content of the marker. The linear regression data for the calibration plots showed a good linear relationship with r=0.99977 for stigmasterol, respectively Satisfactory recoveries of 99.77 % were obtained for stigmasterol.Conclusion: The results obtained in validation assays indicate the accuracy and reliability of the developed HPTLC method for the quantification of stigmasterol in methanolic rhizomes extract of Alpinia calcarata


2016 ◽  
Vol 5 (1) ◽  
pp. 4
Author(s):  
Salah Daoud ◽  
Abdelhalim Bencheikh ◽  
Laarbi Belagraa

A quantitative form of the linear correlation between the high-frequency and static dielectric constants in ANB8-N (N = 2, 3) tetrahedrally coordinated semiconductor materials, and also in I-VII group alkali halides was studied. So, a quasi-linear relationship was found between the high-frequency and the static dielectric constants for some selected II-VI (ZnS, ZnSe, ZnTe and CdTe) and III-V (AlP, AlAs, AlSb,….etc) cubic zincblende type materials, in the other side a weak uphill linear relationship has been found in the case of I-VII (LiF, NaF, LiCl,….etc) group alkali halides compounds. In the case of II-VI and III-V cubic zincblende semiconductors, the linear regression is established with a correlation coefficient ( ) of about 0.98. The significance of the linear regression is given as the probability P <0.0001 of the null hypothesis.


Author(s):  
S. Gurupriya ◽  
L. Cathrine ◽  
P. Pratheema

Objective: A new simple, precise, rapid and selective high‐performance thin‐layer chromatographic (HPTLC) method has been developed for the determination of lupeol in methanolic leaves extract of Andrographis echioides.Methods: As per International Conference on Harmonization (ICH) guidelines we have applied different concentrations of lupeol as standard on HPTLC plates for the quantification of lupeol from the Andrographis echioides leaves. The concentration of standard lupeol was 1 mg/ml.Results: The retention factor of lupeol was found to be 0.55. Linearity was obtained in the range of 5000 ng‐10000 ng for lupeol. The developed and validated HPTLC method was employed for lupeol in methanolic leaves extract of Andrographis echioides for standardization of the content of the marker. The linear regression data for the calibration plots showed a good linear relationship with r=0.99917 for lupeol. Satisfactory recoveries of 99.80 % were obtained for lupeol.Conclusion: The results obtained in validation assays indicate the accuracy and reliability of the developed HPTLC method for the quantification of lupeol in methanolic leaves extract of Andrographis echioides.


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