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2008 | 58 | 4 |

Tytuł artykułu

Antimicrobial activity and cytotoxicity of picolinic acid and selected picolinates as new potential food preservatives

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
In this study antimicrobial activity of picolinic acid (PA), sodium picolinate (PS), potassium picolinate (PP), benzoic acid (BA), sodium benzoate (BS) and potassium benzoate (BP) against Staphylococcus aureus, Pseudomonas aeruginosa, Bacillus subtilis and Candida albicans were measured using microbroth dilution method. Cytotoxicity assay of PS and BS was estimated in the human skin fibroblasts using Thiazolyl Blue Tetrazolium Bromide (MTT) test and DNA-binding assay. PA and PS showed antimicrobial activity at concentrations 0.02 to 0.78 mg/mL at pH=5.0 and 0.19 to 3.13 mg/mL at pH=7.0. Minimal inhibitory concentration (MIC) of BA on tested microorganisms was found at 0.13-0.50 mg/mL (pH=5.0) and about 1 mg/mL at pH=7.0. PA and PS showed strong antimicrobial activity, without significant influence on DNA synthesis and survival of human fibroblasts. The data suggest that PA and PS may represent new potential food preservatives.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

58

Numer

4

Opis fizyczny

p.415-418,fig.,ref.

Twórcy

  • Department of Bromatology, Medical University of Bialystok, Kilinskiego Str. 1, 15-089 Bialystok, Poland
autor
autor

Bibliografia

  • 1. Cai S., Sato K, Shimizu T., Yamabe S., Hiraki M., Sano C., Tamioka H., Antimicrobial activity of picolinic acid against extracellular and intracellular Mycobacterium avium complex and its combined activity with clarithromycin, rifampicin and fluoroquinolones. J. Antimicrob. Chemother., 2006, 57, 1, 85–93.
  • 2. Carmichael J., DeGraff W.G., Gazdar A.F., Minna J.D., Mitchell J.B., Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of chemosensitivity testing. Cancer Res., 1987, 47, 936–942.
  • 3. Dahl J.E., Frangou-Polyzois M.J., Polyzois G.L., In vitro biocompatibility of denture relining materials. Gerodentology, 2006, 23, 17–22.
  • 4. Dazzi C., Candiano G., Massazza S., Ponzetto A., Varesio L., New high-performance liquid chromatographic method for the detection of picolinic acid in biological fluids. J. Chromatogr. B Biomed. Sci. Appl., 2001, 10, 61–68.
  • 5. Dowd P.F., Relative inhibition of insect phenoloxidase by cyclic fungal metabolites from insect and plant pathogens. Nat. Toxins., 1999, 7, 337–341.
  • 6. Espinel–Ingroff A., Pfaller M.A., Antifungal agents and susceptibility testing. 1995, in: Manual of Clinical Microbiology (ed. P.R. Murray). ASM Press, Washington, pp. 1407–1412.
  • 7. Fernandez-Pol J.A., Klos D.J. Hamilton P.D., Antiviral, cytotoxic and apoptotic activities of picolinic acid on human immunodeficiency virus-1 and human herpes simplex virus-2 infected cells. Anticancer Res., 2001, 21, 3773–3776.
  • 8. Kalinowska M., Świsłocka R., Borawska M.H., Piekut J., Lewandowski W., Spectroscopic (FT-IR, FT-Raman, UV) and microbiological studies of di-substituted benzoates of alkali metals. Spectrochim. Acta A, 2008, 70, 126–135.
  • 9. Kirkil G., Hamdi Muz M., Seckin D., Sahin K., Kucuk O., Antioxidant effect of zinc picolinate in patients with chronic obstructive pulmonary disease. Respiro. Med., 2008, 102, 840–844.
  • 10. Koczoń P., Piekut J., Borawska M., Świsłocka R., Lewandowski W., Vibrational and microbiological study on alkaline metal picolinates and o-iodobenzoates. Anal. Bioanal. Chem., 2006, 384, 302–308.
  • 11. Koczoń P., Piekut J., Borawska M., Świsłocka R., Lewandowski W., The relationship between chemical structure and antimicrobial activity of selected nicotinates, p-iodobenzoates, picolinates and isonicotinates. Spectrochim. Acta A, 2005, 61, 1917–1922.
  • 12. Komorowski J.R., Greenberg D., Juturu V., Chromium picolinate does not produce chromosome damage. Toxicol. In Vitro., 2008, 22, 819–26.
  • 13. Musk D.J., Hergenrother P.J., Chelated iron sources are inhibitors of Pseudomonas aeruginosa biofilms and distribute efficiently in an in vitro model of drug delivery to the human lung. J. Appl. Microbiol., 2008, 105, 380–388.
  • 14. Nihei K., Nihei A., Kubo I., Rational design of antimicrobial agents: antifungal activity of alk(en)yl dihydroxybenzoates and dixydroxyphenyl alkanoates. Bioorg. Med. Chem. Lett., 2003, 13, 3993–3996.
  • 15. Park E.-S., Moon W.-S., Song M.-J., Kim M.-N., Chung K.-H., Yoon J.-S., Antimicrobial activity of phenol and benzoic acid derivatives. Int. Biodeterior. Biodegra., 2001, 47, 209–214.
  • 16. Speciale A., Musumeci R., Blandino G., Milazzo I., Caccamo F., Nicoletti G., Minimal inhibitory concentrations and time-kill determination of moxifloxacin against aerobic and anaerobic isolates. Int. J. Antimicrob. Agents., 2002, 19, 111–118.
  • 17. WHO, World Health Organization, IPCS Concise International Chemical Assessment Document No. 26. Benzoic acid and sodium benzoate, 2000, Geneva.
  • 18. Woods G.L., Washington J.A., Antibacterial susceptibility tests: dilution and disk diffusion methods. 1995, in: Manual of Clinical Microbiology (ed. P.R. Murray). ASM Press, Washington, pp. 1334–1336.

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