全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Development and Validation of High Performance Liquid Chromatographic Analysis of Residual N,N-Dimethylformamide in Spent Medium after Biodegradation by Paracoccus denitrificans SD1

DOI: 10.1155/2013/401629

Full-Text   Cite this paper   Add to My Lib

Abstract:

N,N-Dimethylformamide (DMF) is a toxic organic solvent commonly found in the textile and pharmaceutical industrial effluents. The DMF degradation was successfully archived by bacterial strain Paracoccus denitrificans SD1. The study demonstrates the high performance liquid chromatographic (HPLC) approach for the estimation of residual DMF in liquid medium. The investigation mainly focuses on the method development for the detection and quantification of DMF. The bacterium is capable of utilizing DMF (1%?v/v) as the sole source of carbon and nitrogen. Utilization of DMF by the bacterium was investigated at regular intervals of time to check the complete degradation at a particular period. The method was validated based on the precision, accuracy, limit of detection, and limit of quantification. Herein, the method was executed in liquid chromatographic condition which enables direct analysis of aqueous samples from the spent medium avoiding the extraction and prederivatization. This improved method allows estimation of residual DMF from the aqueous medium in adequate ranges of precision and accuracy with 99.17% and 99.43% recovery, respectively. The method was validated by investigating the limit of detection (LOD) and limit of quantification (LOQ) of 0.2 and 0.40?mg/l, respectively. The method was found to be precise for detection of DMF by using liquid chromatography. 1. Introduction N,N-Dimethylformamide (DMF) is a widely used aliphatic organic solvent in chemical, pharmaceutical, and textile industries. Since it is used for recovery of organic compounds, hence considerable amounts of DMF are found in textile and pharmaceutical industrial effluents causing adverse effects on environment and human health [1–4]. Because of its high dielectric constant, it has wide applications in the production of polyurethane, rubber, dyes, wood, leather, films, paper, and pesticides [5]. Globally the demand of DMF is consistently increasing in parallel with industrial activities, resulting in the higher accumulation of DMF in the environment through industrial effluents. It is readily absorbed through oral, dermal, and inhalation exposure [6, 7]. The extents of toxicity induced by DMF are hepatotoxicity, embryotoxicity, teratogenicity, and possible carcinogenicity. Long-term exposure to DMF might also cause irreversible alterations in mitochondrial DNA [5]. The treatment of DMF has gained a considerable attention; it can be recycled by distillation to mother liquors or disposed by incineration [3, 8]. The chemical methods show slower rate of degradation; bioremediation

References

[1]  Y. Hasegawa, M. Matsuo, Y. Sigemoto, T. Sakai, and T. Tokuyama, “Purification and characterization of -Dimethylformamidase from Alcaligenes sp. KUFA-1,” Journal of Fermentation and Bioengineering, vol. 84, no. 6, pp. 543–547, 1997.
[2]  M. J. Twiner, M. Hirst, A. Valenciano, T. R. Zacharewski, and S. J. Dixon, “ -dimethylformamide modulates acid extrusion from murine hepatoma cells,” Toxicology and Applied Pharmacology, vol. 153, no. 2, pp. 143–151, 1998.
[3]  K. C. A. Bromley-Challenor, N. Caggiano, and J. S. Knapp, “Bacterial growth on -dimethylformamide: implications for the biotreatment of industrial wastewater,” Journal of Industrial Microbiology and Biotechnology, vol. 25, no. 1, pp. 8–16, 2000.
[4]  T. H. Kim, Y. W. Kim, S. M. Shin, C. W. Kim, I. J. Yu, and S. G. Kim, “Synergistic hepatotoxicity of -dimethylformamide with carbon tetrachloride in association with endoplasmic reticulum stress,” Chemico-Biological Interactions, vol. 184, no. 3, pp. 492–501, 2010.
[5]  J. Mraz, “N-Acetyl-S-(N-methylcarbamoyl) cysteine (AMCC), the mercapturic acid of -dimethylformamide (DMF): metabolic formation, methods of analysis, application in biological monitoring,” in Mercapturic Acids as Biomarkers of Exposure to Industrial Chemicals, L. Ambrosi, L. Soleo, S. Ghittori, L. Maestri, and M. Imbriani, Eds., pp. 111–118, Maugeri Foundation Books, PI-ME Press, Pavia, Italy, 2001.
[6]  F. Brugnone, L. Perbellini, and E. Gaffuri, “ -dimethylformamide concentration in environmental and alveolar air in an artificial leather factory,” British Journal of Industrial Medicine, vol. 37, no. 2, pp. 185–188, 1980.
[7]  J. Mraz and H. Nohova, “Percutaneous absorption of -dimethylformamide in humans,” International Archives of Occupational and Environmental Health, vol. 64, no. 2, pp. 79–83, 1992.
[8]  L. Dziewit, M. Dmowski, J. Baj, and D. Bartosik, “Plasmid pAMI2 of Paracoccus aminophilus JCM 7686 carries -dimethylformamide degradation-related genes whose expression is activated by a LuxR family regulator,” Applied and Environmental Microbiology, vol. 76, no. 6, pp. 1861–1869, 2010.
[9]  O. Ghisalba, P. Cevey, M. Kuenzi, and H. P. Schar, “Biodegradation of chemical waste by specialized methylotrophs, an alternative to physical methods of waste disposal,” Conservation and Recycling, vol. 8, no. 1-2, pp. 47–71, 1985.
[10]  T. Urakami, H. Araki, H. Oyanagi, K. I. Suzuki, and K. Komagata, “Paracoccus aminophilus sp. nov. and Paracoccus aminovorans sp. nov., which utilize -dimethylformamide,” International Journal of Systematic Bacteriology, vol. 40, no. 3, pp. 287–291, 1990.
[11]  Y. Veeranagouda, P. V. Emmanuel Paul, P. Gorla, D. Siddavattam, and T. B. Karegoudar, “Complete mineralisation of dimethylformamide by Ochrobactrum sp. DGVK1 isolated from the soil samples collected from the coalmine leftovers,” Applied Microbiology and Biotechnology, vol. 71, no. 3, pp. 369–375, 2006.
[12]  S. Swaroop, P. Sughosh, and G. Ramanathan, “Biomineralization of -dimethylformamide by Paracoccus sp. strain DMF,” Journal of Hazardous Materials, vol. 171, no. 1–3, pp. 268–272, 2009.
[13]  S. S. Kumar, M. S. Kumar, D. Siddavatam, and T. B. Karegoudar, “Generation of continuous packed bed reactor with PVA-alginate blend immobilized Ochrobactrum sp. DGVK1 cells for effective removal of -dimethylformamide from industrial effluents,” Journal of Hazardous Materials, vol. 199-200, pp. 58–63, 2012.
[14]  D. Siddavattam, T. B. Karegoudar, S. K. Mudde et al., “Genome of a novel isolate of Paracoccus denitrificans capable of degrading -Dimethylformamide,” Journal of Bacteriology, vol. 193, pp. 5598–5599, 2011.
[15]  C. F. Cullis and D. J. Waddington, “The colorimetric determination of secondary amines,” Analytica Chimica Acta, vol. 15, pp. 158–163, 1956.
[16]  H. P. Sch?r, W. Holzmann, G. M. Ramos, and O. Ghisalba, “Purification and characterization of -dimethylformamidease from Pseudomonas DMF3/3,” Europien Journal of Biochemistry, vol. 158, pp. 469–475, 1986.
[17]  United States Pharmacopeia XXI I, United States Pharmacopeial Convention, Rockvilie, Md, USA, 1990.
[18]  Validation of Compedial Assays-Guidelines, Pharmacopeial Convention, Rockvilie, Md, USA, 1985.
[19]  E. Armaforte, S. Carri, G. Ferri, and M. F. Caboni, “High-performance liquid chromatography determination of phenyllactic acid in MRS broth,” Journal of Chromatography A, vol. 1131, no. 1-2, pp. 281–284, 2006.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133