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1.
Molecules ; 17(9): 10094-107, 2012 Aug 24.
Article in English | MEDLINE | ID: mdl-22922280

ABSTRACT

Pomegranate has attracted interest from researchers because of its chemical composition and biological properties. It possesses strong antioxidant activity, with potential health benefits, and also antimicrobial properties. The aim of this study was to produce microparticles containing pomegranate extract by the spray-drying technique, utilizing alginate or chitosan as encapsulating agents. Characterization and antifungal assays were carried out. Production yields were about 40% for alginate microparticles and 41% for chitosan. Mean diameters were 2.45 µm and 2.80 µm, and encapsulation efficiencies were 81.9% and 74.7% for alginate and chitosan microparticles, respectively. The spray-drying process preserved the antifungal activity against Candida albicans. These results could be useful for developing dosage forms for treating candidiasis, and should be further investigated in in vivo models.


Subject(s)
Antifungal Agents/pharmacology , Candida albicans/drug effects , Lythraceae/chemistry , Microspheres , Plant Extracts/pharmacology , Animals , Biofilms/drug effects , Cell Line , Chitosan/chemistry , Chlorocebus aethiops , Pharmaceutical Preparations , Vero Cells
2.
Res Microbiol ; 161(7): 534-40, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20541606

ABSTRACT

Activity-guided repeated fractionation of crude hydro alcoholic extract prepared from the fruit peel of Punica granatum on a silica-gel column yielded a compound that exhibited strong antifungal activity against Candida spp. Based on spectral analyses, the compound was identified as punicalagin. Punicalagin showed strong activity against Candida albicans and Candida parapsilosis, with MICs of 3.9 and 1.9 microg/ml, respectively. The combination of punicalagin and fluconazole showed a synergistic interaction. MIC for fluconazole decreased twofold when combined with the extract. The FIC index was 0.25. The synergism observed in disk-diffusion and checkerboard assays was confirmed in time-kill curves. The effect of punicalagin on the morphology and ultrastructure in treated yeast cells was examined by scanning and transmission electron microscopy. An irregular budding pattern and pseudohyphae were seen in treated yeasts. By transmission electron microscopy, treated cells showed a thickened cell wall, changes in the space between cell wall and the plasma membrane, vacuoles, and a reduction in cytoplasmic content. Since the punicalagin concentration effective in vitro is achievable in vivo, the combination of this agent with fluconazole represents an attractive prospect for the development of new management strategies for candidiasis, and should be investigated further in in vivo models.


Subject(s)
Antifungal Agents/pharmacology , Candida albicans/drug effects , Candida/drug effects , Fluconazole/pharmacology , Hydrolyzable Tannins/pharmacology , Lythraceae/chemistry , Antifungal Agents/chemistry , Antifungal Agents/isolation & purification , Candida/ultrastructure , Candida albicans/ultrastructure , Chromatography, Thin Layer , Drug Resistance, Fungal , Drug Synergism , Hydrolyzable Tannins/chemistry , Hydrolyzable Tannins/isolation & purification , Microbial Sensitivity Tests , Microscopy, Electron, Scanning , Microscopy, Electron, Transmission , Plant Epidermis/chemistry
3.
Antonie Van Leeuwenhoek ; 97(2): 201-5, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19882381

ABSTRACT

Berberine with and without fluconazole was tested by an agar disk diffusion assay in which clinical isolates of Candida albicans were applied onto yeast extract-peptone-dextrose agar plate. Berberine, which had no intrinsic antifungal activity at the concentration tested, exerted a powerful antifungal activity in combination of fluzonazole. Combinations of berberine and fluconazole were also tested by the checkerboard assay to determine whether they had favorable or unfavorable antifungal interactions. The MIC of fluconazole was 1.9 microg/ml when the drug was tested alone and decreased to 0.48 microg/ml in the presence of berberine concentrations of 1.9 microg/ml. However, berberine at concentrations of >1.9 microg/ml combined with a fluconazole supra-MIC (i.e., >1.9 microg/ml) eliminated the residual turbidity in the incubation wells. This endpoint fitted to the definition of MIC-0 (optically clear wells) and reflected the absence of a trailing effect, which is the result of a residual growth at fluconazole concentrations greater than the MIC.


Subject(s)
Antifungal Agents/pharmacology , Berberine/pharmacology , Candida albicans/drug effects , Fluconazole/pharmacology , Candida albicans/isolation & purification , Candidiasis/microbiology , Drug Synergism , Humans , Microbial Sensitivity Tests
4.
Molecules ; 14(3): 1171-82, 2009 Mar 16.
Article in English | MEDLINE | ID: mdl-19325517

ABSTRACT

The chemical composition of the essential oil obtained from the leaves of Piperovatum Vahl by hydrodistillation was analyzed by GC-MS. The main constituents found were delta-amorphene (16.5 %), cis-muurola-4(14),5-diene (14.29 %) and gamma-muurolene(13.26%). The crude extracts and isolated compounds were screened for their antimicrobial activity. Hydroalcoholic extracts of different parts of Piper ovatum Vahl, essential oil andamides isolated from leaves were tested against Gram-positive and Gram-negative bacteria and Candida species. All extracts and amides were active against Bacillus subtilis andCandida tropicalis, including clinical strains. Essential oil was active against C. tropicalis.These amides showed an inhibitory effect on the adherence of C. tropicalis ATCC 28707 on cover glasses at 10 microg/mL, but did not show morphological alterations at the tested concentrations. Amides were identified as piperovatine and piperlonguminine, and showed MIC values of 15.6 and 31.2 microg/mL to B. subtilis and 3.9 microg/mL to C. tropicalis, and low toxic effects to Vero cells and macrophages.


Subject(s)
Anti-Infective Agents/chemistry , Piper/chemistry , Animals , Anti-Infective Agents/pharmacology , Candida/drug effects , Chlorocebus aethiops , Gas Chromatography-Mass Spectrometry , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , Humans , Macrophages/drug effects , Microbial Sensitivity Tests , Oils, Volatile/chemistry , Oils, Volatile/pharmacology , Plant Extracts/chemistry , Plant Extracts/pharmacology , Plant Leaves/chemistry , Vero Cells/drug effects
5.
Int J Hyg Environ Health ; 211(5-6): 504-9, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18206422

ABSTRACT

The bacteriological quality of tap water from municipal water supplies, 20-L bottles of mineral water from water dispensers and samples collected from new 20-L bottles of mineral water were comparatively studied. Total coliforms, termotolerant coliforms, Escherichia coli, fecal streptococci, Pseudomonas aeruginosa, Staphylococcus spp. and heterotrophic plate count were enumerated. The results showed that 36.4% of the tap water samples from municipal water systems and 76.6% of the 20-L bottles of mineral water from water dispensers were contaminated by at least one coliform or indicator bacterium and/or at least one pathogenic bacterium. The bacteriological quality of municipal tap water is superior when compared with the 20-L bottles of mineral water collected from water dispensers and samples collected from new 20-L bottles of mineral water before installation in the dispensers. This highlights the need for an improved surveillance system for the bottled water industry. For the municipal water systems, it is recommended to perform the Pseudomonas enumeration periodically, in addition to the routine data collected by most systems.


Subject(s)
Carbonated Beverages/microbiology , Enterobacteriaceae/isolation & purification , Water Microbiology , Water Supply , Brazil , Colony Count, Microbial , Enterococcus/isolation & purification , Escherichia coli/isolation & purification , Food Industry , Humans , Pseudomonas aeruginosa/isolation & purification , Staphylococcus/isolation & purification
6.
Antonie Van Leeuwenhoek ; 93(4): 323-34, 2008 May.
Article in English | MEDLINE | ID: mdl-18038252

ABSTRACT

Pseudomonas aeruginosa isolates from tap water, mineral water, and artesian well water were investigated for their ability to produce different potential virulence factors or markers such as hemolysins, hemaglutinins, cytotoxins and their ability to adhere to epithelial cells and to abiotic surfaces. The susceptibility to antibiotics, human serum sensitivity and the survival of P. aeruginosa isolates in a chlorinated environment were also examined. Of the 30 isolates tested, 16 possessed the capacity to adhere to abiotic surfaces, and 28 to adhere to epithelial cells; 30 were capable of producing hemolysins, 27 produced cytotoxins, 9 hemagglutinins, and 18 were classified as serum-resistant. For the lowest concentration of chlorine (0.2 mg/l) tested, no killing of biofilm bacteria could be discerned, even after prolonged exposure to the agent. Although all the drinking water isolates were susceptible to aztreonam, cefepime, ceftazidime, ciprofloxacin, imipenem, meropenem, piperacillin-tazobactam, and polymyxin, the P. aeruginosa isolates were resistant to one or more antibiotics. The increasing prevalence of resistance in the isolates from environmental sources may have important therapeutic implications. A notable proportion of the P. aeruginosa isolates from drinking water were able to develop virulence factors, and the incidence of virulence properties was not statistically different among the three sources. A more extensive study of the virulence properties of this bacterium by toxic assays on animals should be explored. Still more interesting would be toxicity assays on immuno-deficient animals with isolates from drinking water in order to better understand the health risk these bacteria may present.


Subject(s)
Pseudomonas aeruginosa/isolation & purification , Pseudomonas aeruginosa/pathogenicity , Virulence Factors/metabolism , Water Microbiology , Animals , Anti-Bacterial Agents/pharmacology , Bacterial Adhesion , Biofilms/drug effects , Biofilms/growth & development , Blood Bactericidal Activity , Cheek/microbiology , Chlorine/pharmacology , Chlorocebus aethiops , Cytotoxins/metabolism , Drug Resistance, Bacterial , Epithelial Cells/microbiology , Hemagglutination , Hemagglutinins/metabolism , Hemolysin Proteins/metabolism , Hemolysis , Humans , Hydrophobic and Hydrophilic Interactions , In Vitro Techniques , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/drug effects , Pseudomonas aeruginosa/physiology , Vero Cells , Water Supply
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