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Current Analytical Chemistry

Editor-in-Chief

ISSN (Print): 1573-4110
ISSN (Online): 1875-6727

Research Article

Development and Validation of an Eco-Friendly and Low-Cost Method for the Quantification of Cefepime Hydrochloride in Powder for Injectable Solution Using Infrared (IR) Spectroscopy

Author(s): Danilo F. Rodrigues* and Hérida R.N. Salgado

Volume 16, Issue 4, 2020

Page: [456 - 464] Pages: 9

DOI: 10.2174/1573411014666180704122816

Price: $65

Abstract

Background: A simple, eco-friendly and low-cost Infrared (IR) method was developed and validated for the analysis of Cefepime Hydrochloride (CEF) in injectable formulation. Different from some other methods, which employ organic solvents in the analyses, this technique does not use these types of solvents, removing large impacts on the environment and risks to operators.

Objective: This study aimed at developing and validating a green analytical method using IR spectroscopy for the determination of CEF in pharmaceutical preparations.

Methods: The method was validated according to ICH guidelines and the quantification of CEF was performed in the spectral region absorbed at 1815-1745 cm-1 (stretching of the carbonyl group of β- lactam ring).

Results: The validated method showed to be linear (r = 0.9999) in the range of 0.2 to 0.6 mg/pellet of potassium bromide, as well as for the parameters of selectivity, precision, accuracy, robustness and Limits of Detection (LOD) and Quantification (LOQ), being able to quantify the CEF in pharmaceutical preparations. The CEF content obtained by the IR method was 103.86%.

Conclusion: Thus, the method developed may be an alternative in the quality control of CEF sample in lyophilized powder for injectable solution, as it presented important characteristics in the determination of the pharmaceutical products, with low analysis time and a decrease in the generation of toxic wastes to the environment.

Keywords: Cefepime hydrochloride, green chemistry, pharmaceutical analysis, quality control, spectroscopy, validation.

Graphical Abstract

[1]
Sanders, W.E.J.R., Jr; Tenney, J.H.; Kessler, R.E. Efficacy of cefepime in the treatment of infections due to multiply resistant Enterobacter species. Clin. Infect. Dis., 1996, 23(3), 454-461.
[http://dx.doi.org/10.1093/clinids/23.3.454] [PMID: 8879764]
[2]
Diekema, D.J.; Pfaller, M.A.; Jones, R.N.; Doern, G.V.; Winokur, P.L.; Gales, A.C.; Sader, H.S.; Kugler, K.; Beach, M. Survey of bloodstream infections due to gram-negative bacilli: frequency of occurrence and antimicrobial susceptibility of isolates collected in the United States, Canada, and Latin America for the SENTRY Antimicrobial Surveillance Program, 1997. Clin. Infect. Dis., 1999, 29(3), 595-607.
[http://dx.doi.org/10.1086/598640] [PMID: 10530454]
[3]
Sweetman, S.C. Martindale: The complete drug reference, 36th ed; RPS Publishing: London, 2009.
[4]
El-Rabbat, N.A.; Abdel-Wadood, H.M.; Sayed, M.; Mousa, H.S. Spectrophotometric analysis of cefepime through its Hg(I) complex. Bull. Pharm. Sci., 2012, 35, 55-65.
[http://dx.doi.org/10.21608/bfsa.2012.64602]
[5]
Silverstein, R.M.; Webster, F.X.; Kiemle, D. Identificação espectrofotométrica de compostos orgânicos 7th ed; LTC: Rio de Janeiro, 2007
[6]
Brazilian Pharmacopeia, 5th ed; Agência Nacional de Vigilância Sanitária: Brasília, 2010.
[7]
Pavia, D.L.; Lampman, G.M.; Kriz, G.S.; Vyvyan, J.R. Introdução à Espectroscopia, 4th ed; Cengage Learning: São Paulo, 2010.
[8]
Lopes, W.A.; Fascio, M. Esquema para interpretação de espectros de substâncias orgânicas na região do infravermelho. Quim. Nova, 2004, 27(4), 670-673.
[http://dx.doi.org/10.1590/S0100-40422004000400025]
[9]
Zhang, X.B.; Feng, Y.C.; Hu, C.Q. Feasibility and extension of universal quantitative models for moisture content determination in β-lactam powder injections by near-infrared spectroscopy. Anal. Chim. Acta, 2008, 630(2), 131-140.
[http://dx.doi.org/10.1016/j.aca.2008.09.050] [PMID: 19012824]
[10]
Ferdous, S.; Sultan, M.Z.; Bashar, T.; Rahman, A.; Islam, M.S. In vitro and in vivo studies of drug-drug interaction between metformin and cefepime. Pharm. Anal. Acta, 2015, 6(348), 1-5.
[11]
Bugay, D.E.; Newman, A.W.; Findlay, W.P. Quantitation of cefepime.2HCl dihydrate in cefepime.2HCl monohydrate by diffuse reflectance IR and powder X-ray diffraction techniques. J. Pharm. Biomed. Anal., 1996, 15(1), 49-61.
[http://dx.doi.org/10.1016/0731-7085(96)01796-7] [PMID: 8895076]
[12]
Moreno, A.H.; Salgado, H.R.N. Development and validation of the quantitative analysis of ceftazidime in powder for injection by infrared spectroscopy. Phys. Chem., 2012, 2(1), 6-11.
[http://dx.doi.org/10.5923/j.pc.20120201.02]
[13]
Tótoli, E.G.; Salgado, H.R.N. Development and validation of the quantitative analysis of ampicillin sodium in powder for injection by fourier-transform infrared spectroscopy (FT-IR). Phys. Chem., 2012, 2(6), 103-108.
[http://dx.doi.org/10.5923/j.pc.20120206.04]
[14]
Vieira, D.C.M.; Ricarte, P.C.; Salgado, H.R.N. Development and validation of the quantitative analysis of cefuroxime sodium in powder for injection by infrared spectroscopy. Adv. Anal., 2012, 2(6), 80-87.
[15]
Kogawa, A.C.; Salgado, H.R.N. Development and validation of infrared spectroscopy method for the determination of darunavir in tabets. Phys. Chem., 2013, 3(1), 1-6.
[16]
Corrêa, J.C.R.; Salgado, H.R.N. A platform for designing quantitative infrared spectrophotometric method for drugs and pharmaceuticals analysis: a rediscover for an ecological and safer technique in the routine quality control laboratories. World J. Pharm. Pharm. Sci., 2014, 3(6), 2056-2059.
[17]
Kogawa, A.C.; Aguiar, F.A.; Gaitani, C.M.; Salgado, H.R.N. Validation of a stability indicating capillary electrophoresis method for the determination of darunavir in tablets and comparison with the of infrared absorption spectroscopic method. World J. Pharm. Pharm. Sci., 2014, 3(6), 283-297.
[18]
Kogawa, A.C.; Mello, N.P.; Salgado, H.R.N. Quantification of doxycycline in raw material by an eco-friendly method of infrared spectroscopy. Pharm. Anal. Acta, 2016, 7(2), 1-4.
[19]
Natori, J.S.H.; Tótoli, E.G.; Salgado, H.R.N. Development and validation of a green analytical method for the determination of norfloxacin in raw material by FTIR spectrophotometry. J. AOAC Int., 2016, 99(6), 1533-1536.
[http://dx.doi.org/10.5740/jaoacint.16-0177] [PMID: 28206879]
[20]
De Marco, B.A.; Salgado, H.R.N. Development and validation of an innovative method for the determination of cefadroxil monohydrate in capsules. Phys. Chem., 2016, 6(3), 67-74.
[21]
Consortti, L.P.; Salgado, H.R.N. Green method for quantification of sodium cefotaxime in lyophilized powder by infrared spectroscopy. J. Pharm. Sci. Emerg. Drugs, 2017, 5(1), 2-6.
[http://dx.doi.org/10.4172/2380-9477.1000118]
[22]
Ministério da Saúde Resolução RDC 899 (May 29 2003).
Diário Oficial da União; Brasília, 2003.
[23]
International Conference on Harmonization (ICH). Validation of analytical procedures: Text and Methodology Q2 (R1), International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use: Geneva, 2005
[24]
Association of Official Analytical Chemists. Official Methods of Analysis, 17th ed; AOAC INTERNATIONAL: Gaithersburg, 2002, p. 1.
[25]
Montgomery, D.C. Design and Analysis of Experiments, 7th ed; John Wiley & Sons: New York, 2009.
[26]
Neto, B.B.; Scarminio, I.S.; Bruns, R.E. Como fazer experimentos, 4th ed; Bookman: Porto Alegre, 2010.
[27]
Nolasco, F.R.; Tavares, G.A.; Bendassolli, J.A. Implantação de programas de gerenciamento de resíduos químicos laboratoriais em universidades: análise crítica e recomendações. Eng. Sanit. Ambient., 2006, 11(2), 118-124.
[http://dx.doi.org/10.1590/S1413-41522006000200004]
[28]
U.S. Pharmacopeia, 37th ed; U.S. Pharmacopoeial Convention, Inc.: Rockville, 2014.

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