Spot-test identification and rapid quantitative sequential analysis of dipyrone

Main Article Content

Matthieu Tubino
Adriane Cristina Biondo
Marta Maria Duarte Carvalho Vila
Leonardo Pezza
Helena Redigolo Pezza

Abstract

A qualitative spot-test and tandem quantitative analysis of dipyrone in the bulk drug
and in pharmaceutical preparations is proposed. The formation of a reddish-violet  color indicates a positive result. In sequence a quantitative procedure can be performed in the same flask. The quantitative results obtained were statistically compared with those obtained with the method indicated by the Brazilian  Pharmacopoeia, using the Student’s t and the F tests. Considering the concentration in a 100 μL aliquot, the qualitative visual limit of detection is about 5×10-6 g; instrumental LOD ≅ 1.4×10-4 mol L-1 ; LOQ ≅ 4.5×10-4 mol L-1.

Metrics

Metrics Loading ...

Article Details

How to Cite
Tubino, M., Biondo, A. C., Vila, M. M. D. C., Pezza, L., & Pezza, H. R. (2010). Spot-test identification and rapid quantitative sequential analysis of dipyrone. Eclética Química, 35(1), 41–46. https://doi.org/10.26850/1678-4618eqj.v35.1.2010.p41-46
Section
Original articles

References

Brazilian Pharmacopoeia, 3rd ed., Organização Andrei Editora, São Paulo, Brazil, 1977, p 406-8.

I.M. Benseñor, São Paulo Med. J., 119 (2001) 190.

H. Ergün, D. A. C. Frattarelli and J. Aranda, J. Pharmaceut. Biomed., 35 (2004) 479.

P. Danielli, and M.B Leal, Rev. Bras. Farm., 84 (2003) 17.

Y. Bentur, and O. Cohen, J. Toxicol.-Clin. Toxic., 42 (2004) 261.

S. C. Pierre, R. Schmidt, C. Brenneis, M. Michaelis, G. Geisslinger, and K. Scholich, Br. J. Pharmacol., 151 (2007) 494.

G. Suarez-Kurtz , F.M. Ribeiro, R.C.E. Estrela, F.L. Vicente, and C J. Struchiner, Braz. J. Med. Biol. Res., 34 (2001) 1475.

Brasil, Anvisa, Agência Nacional de Vigilância Sanitária, Rev. Saúde Pública, 38 (2004) 748.

F.G.D. Vieira, J. M. Crubellate, I.G. Silva, and W.R. Silva, RAE eletron.,1 (2002) 1.

H. Senyuva, I. Aksahin, S. Ozcan, and B.V. Kabasakal, Anal. Chim. Acta, 547 (2005)73-7.

K.A. Sakiara, L. Pezza, C. B. Melios, H. R. Pezza, and M. Moraes, Farmaco, 54 (1999) 629.

J. L. F. C. Lima, S. M. O. Sá, J. L. Santos, and E. A. G. Zagatto, J. Pharmaceut. Biomed., 32 (2003)1011.

L. H. Marcolino Jr, R. A. Souza, O. Fatibello Filho, and F.C. Moraes, Anal. Lett., 38 (2005) 2315.

A.V. Pereira, L. Penckowski, M. Vosgerau, and M. F. Sassá, Quím. Nova 25 (2002)553.

A. P. Nascimento, M. G. Trevisan, E. R. M. Kedor-Hackmann, and R. J. Poppi, Anal. Lett., 40 (2007) 975.

J. S. Albuquerque, V. L. Silva, F. Lima, A. Araújo, and M. C. B. S. M.Montenegro, Anal. Sci., 19 (2003) 692

T. R. L. C. Paixão, C. R. Matos, and M. Bertotti, Talanta, 61 (2003) 725.

E. P. Medeiros, S.L. Castro, F. M. Formiga, S. R. B. Santos, M. C. U. Araújo, and V. B. Nascimento, Microchem. J., 78 (2004) 91.

L. H. Marcolino Jr, V. G. Bonifácio, and O. Fatibello Filho, Quím. Nova, 28 (2005) 783.

M. F. S Teixeira, L. H. Marcolino Jr., O. Fatibello Filho, E. R. Dockal, and E. T. G. Cavalheiro, J. Braz. Chem. Soc., 15 (2004) 803.

P. L.Weinert, L. Pezza, and H.R. Pezza, J. Braz. Chem. Soc., 18 (2007) 846

F. Feigl, Spot Tests in Organic Analysis, 7th ed., Elsevier, Amsterdan, 1966, p. 434-36 and 635.

L. Pezza, M. Tubino, C. B. Melios, and H. R. Pezza, Anal. Sci., 16 (2000) 313.

K. Eckschlager, Errors, Measurement and Results in Chemical Analysis, Van Nostrand Reinhold Company, London, 1972, p. 109-120.

P. Karrer, Organic Chemistry, 4th ed.; Wiley, New York, 1950, p. 798.

P. E. Georghiou, and C.K. Ho, Can. J. Chem., 67 (1989) 871