scholarly journals In vitro antifungal activity of pneumocandin L-743,872 against a variety of clinically important molds.

1997 ◽  
Vol 41 (8) ◽  
pp. 1835-1836 ◽  
Author(s):  
M Del Poeta ◽  
W A Schell ◽  
J R Perfect

The in vitro activity of the new antifungal drug pneumocandin L-743,872 against 55 isolates of clinically important molds was examined by an adapted macrobroth dilution method for yeasts. Pneumocandin L-743,872 exhibited in vitro antifungal activity against Alternaria sp., Aspergillus flavus, Aspergillus fumigatus, Curvularia lunata, Exophiala jeanselmei, Fonsecaea pedrosoi, Paecilomyces variotii, and Scedosporium apiospermum. The drug appeared to lack significant in vitro inhibitory activity against Fusarium oxysporum, Fusarium solani, Rhizopus arrhizus, Paecilomyces lilacinus, and Scedosporium prolificans.

2008 ◽  
Vol 3 (9) ◽  
pp. 1934578X0800300 ◽  
Author(s):  
Mehrdad Iranshahi ◽  
Abdolmajid Fata ◽  
Bahareh Emami ◽  
Bibi Mohadeseh Jalalzadeh Shahri ◽  
Bibi Sedigheh Fazly Bazzaz

The increase in dermatophytoses and the fact that some patients do not respond well to therapy make it necessary to find new antifungal agents. As part of our ongoing studies on medicinal plants from Iran, we studied antidermatophytic activities of Ferula latisecta essential oil, which had shown considerable antifungal activity in preliminary antimicrobial screening. Antifungal activity was evaluated by determination of MIC values using the agar dilution method on type strains of Candida albicans and dermatophytes. The composition of the oil was characterized by GC and GC/MS analyses. The essential oil was rich in polysulfides (75.2%) and exhibited good activity against Trichophyton rubrum and T. verrucosom for about three weeks, with a MIC value 96 μg/mL. The oil showed antifungal activity, especially against dermatophytes, and the activity is probably related to the sulfur-containing components of the oil. This study has identified that the polysulfides-rich essential oil of Ferula latisecta fruits has activity against a range of human pathogenic dermatophytes, justifying future clinical trials to validate its use as a therapeutic alternative for dermatophytosis.


2018 ◽  
Vol 13 (9) ◽  
pp. 1934578X1801300 ◽  
Author(s):  
Daniele Fraternale ◽  
Donata Ricci

The present study reports the results of gas chromatography-mass spectrometry (GC/MS) analyses of the essential oil from flowering aerial parts of Cotinus coggygria Scoop. (Anacardiaceae), as well as its in vitro antifungal activity against nine plant pathogenic fungi. Moreover, the essential oil was evaluated for its antifungal activity using the agar dilution method, and also MICs (minimum inhibitory concentrations) and MFCs (minimum fungicidal concentrations) were determined. The major compounds identified by GC-MS were limonene (49.2%), (Z)-β-ocimene (13.6%), α-pinene (8.8%) and (E)-β-ocimene (5.9%). The oil showed in vitro antifungal activity against some species of the Fusarium genus, Botrytis cinerea, and Alternaria solani. Our study indicates that the oil of C. coggygria could be used as a control agent for plant pathogenic fungi in natural formulations.


2002 ◽  
Vol 9 (1-2) ◽  
pp. 91-96 ◽  
Author(s):  
Libor Dostál ◽  
Aleš Růžička ◽  
Roman Jambor ◽  
Vladimír Buchta ◽  
Petra Kubanová ◽  
...  

The in vitro antifungal activity of compounds 1-3 ({[(CH3)2NCH2]2C6H3}R2SnX; (where X=Cl, R=n-Bu for 1, X=Br, R=n-Bu for 2 and x=PF6, R=n=Bu for 3)) was estimated with the help of a modified microdilution format of the M27-A guidelines and was compared with in vitro activity of their diphenyltin(IV) analogues 4 and 5 (where X=Br, R=Ph for 4 and X=PF6, R=Ph for 5), and of drugs currently in clinical use (ketoconazole, fluconazole and amphotericin B). It was found that in coordinating solvents the more soluble derivative 2 is less active than the phenyl one (4), and compounds 1 and 3 are even inactive.In this paper, the in vitro antitumour activity of ionic diphenyltin(IV) complexes 4 and 5 against seven tumoural cell lines of human origin is also reported. The preparation and characterization (H1, C13 and Sn119 NMR spectroscopy and electrospray ionization mass spectrometry) of the novel compound 3 is mentioned too.


Author(s):  
Hassan Thoulfikar A. Alamir ◽  
M. E. L. A. Shayoub ◽  
Wisal G. Abdalla ◽  
Eltayeb Suliman Elamin

In vitro activity of miconazole, salicylic acid and benzoic acid against T.richophyton mentagrophytes was done on Sabouraud’s dextrose agar. The inhibition zones were measured in cm. 2.8 cm, 1.5 cm and no inhibition zone were reported for miconazole, salicylic acid and benzoic acid respectively. Synergistic effect of salicylic acid and benzoic acid against T. mentagrophytes was done using two different bases of cream lanette 20% and aqueous cream 30/70. Four different formula each one contain 2% miconazole with different concentrations of salicylic acid and benzoic acid were used. Biggest inhibition zone (5 cm) was observed of lanette cream which contains 2% miconazole, 3% salicylic acid and 6% benzoic acid.


Author(s):  
Léon W. Nitiema ◽  
Fabrice W. Nikiema ◽  
Drissa Sérémé ◽  
Pierre A. E. D. Sombié

Aims: This study was undertaken to investigate the antifungal activities of Securidaca longepedunculata and Acacia gourmaensis bark hydro-ethanolic extract against Fusarium solani, Fusarium moniliforme and Curvularia lunata and to evaluate the percentages of germination and infection of infected rice seeds. Methods: Different extract concentrations ranging from 0.25, 0.5 and 1% were tested during 15 days using poisoned food technique method for in vitro antifungal activity against above three fungal strains. The same concentrations of extract were used to evaluate in vivo antifungal activity on rice seeds infected by these three fungal strains. Results: The extract of Securidaca longepedunculata had antifungal effect on Fusarium solani and Fusarium moniliforme and completely inhibited its mycelial growth at all tested concentrations (0.25, 0.5 and 1%). Curvularia lunata mycelial growth was inhibited of 84.7% by 1% Securidaca longepedunculata extract after five days of culture. However, mycelial growth of F. solani, F. moniliforme and C. lunata were increased with increasing concentration of Acacia gourmaensis extract. It has been observed that when Securidaca longepedunculata hydro-ethanolic extract concentration increased up to 1%, seeds germination percentage decreased for all infection. In contrast, the opposite was observed for Acacia gourmaensis extract. Likewise, seeds infection decreased with the highest concentration (1%) of Securidaca longepedunculata for all infection, whereas the opposite was observed with Acacia gourmaensis extract. Conclusion: This study showed that S. longepedunculata hydro-ethanolic extract has more antifungal activity against seed-borne fungi (F. solani, F. moniliforme and C. lunata) than A. gourmaensis in vitro and in vivo. Results show that Securidaca longepedunculata hydro-ethanolic bark extract can be used as a potential antifungal agent in the management of some rice fungal diseases. Acacia gourmaensis extract, at low concentration, could be used in rice seed treatment to increase seed germination.


2000 ◽  
Vol 55 (7-8) ◽  
pp. 534-539 ◽  
Author(s):  
Helen Skaltsa ◽  
Diamanto Lazari ◽  
Begoña Garcia ◽  
José R. Pedro ◽  
Marina Sokovic ◽  
...  

Abstract The aerial parts of Centaurea achaia afforded, in addition to several known sesquiterpene lactones and sesquiterpene hydroxyesters, a new germacranolide and a new elemanolide. Their structures were determined as the 8 α-O-(4,5-dihydroxy-tigloyloxy) esters of salonitenolide and of 11,13-dihydromelitensin, respectively. The in vitro antifungal activity of most compounds was tested against nine fungal species using the micro-dilution method. All the tested compounds showed strong antifungal activity.


Toxins ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 579 ◽  
Author(s):  
Mariana Paiva Rodrigues ◽  
Andrea Luciana Astoreca ◽  
Águida Aparecida de Oliveira ◽  
Lauranne Alves Salvato ◽  
Gabriela Lago Biscoto ◽  
...  

Aspergillus carbonarius is a saprobic filamentous fungus, food spoiling fungus and a producer of ochratoxin A (OTA) mycotoxin. In this study, the in vitro antifungal activity of neem oil (0.12% p/p of azadirachtin) was evaluated against the growth of six strains of A. carbonarius and the production of OTA. Four different concentrations of neem oil were tested in addition to three incubation times. Only the concentration of 0.3% of neem oil inhibited more than 95% of the strain’s growth (97.6% ± 0.5%), while the use of 0.5% and 1.0% of neem oil showed lower antifungal activity, 40.2% ± 3.1 and 64.7% ± 1.1, respectively. There was a complete inhibition of OTA production with 0.1% and 0.3% neem oil in the four strains isolated in the laboratory from grapes. The present study shows that neem essential oil can be further evaluated as an auxiliary method for the reduction of mycelial growth and OTA production.


1997 ◽  
Vol 41 (4) ◽  
pp. 841-843 ◽  
Author(s):  
S A Radford ◽  
E M Johnson ◽  
D W Warnock

The in vitro activity of voriconazole was compared with that of itraconazole. Eighty-six isolates of pathogenic molds belonging to 23 species were tested by an agar dilution method in High Resolution medium. Voriconazole was more active than itraconazole against a number of hyaline molds, including several Fusarium spp. and Scedosporium prolificans. Voriconazole and itraconazole showed comparable good activity against several hyaline molds, including Penicillium marneffei and Scedosporium apiospermum, and a number of dematiaceous molds, including Bipolaris australiensis, Cladophialophora bantiana, several Exophiala spp., and several Fonsecaea spp. Our results suggest that voriconazole could be effective against a wide range of mold infections in humans.


2014 ◽  
Vol 9 (7) ◽  
pp. 1934578X1400900 ◽  
Author(s):  
Daniele Fraternale ◽  
Donata Ricci

The present study reports the results of gas chromatographic-mass spectrometric (GC/MS) analyses of the essential oils from the aerial parts of Ballota nigra L. ssp foetida (Lamiaceae) collected at flowering and fruiting times, as well as their in vitro antifungal activity against nine plant pathogenic fungi. Moreover, the essential oils were evaluated for their antifungal activity using the agar dilution method, and also MICs (minimum inhibitory concentrations) and MFCs (minimum fungicidal concentrations) were determined. The major compounds identified in the flowering and fruiting aerial parts oils respectively were β-caryophyllene (22.6% and 21.8%), caryophyllene oxide (18.0% and 20.5%) and germacrene-D (16.5 and 13.1%). The oils showed in vitro antifungal activity against some species of Fusarium, Botrytis cinerea, and Alternaria solani. Our study indicates that the oil of B. nigra ssp foetida could be used as a control agent for plant pathogenic fungi in natural formulations.


2019 ◽  
Vol 2 (3) ◽  
pp. 42-44
Author(s):  
Aarti Patil ◽  
Sadat Quazi

The present study was undertaken to evaluate in-vitro antifungal activity of Semecarpus anacardium Linn. oil against four fungal pathogens, viz. Curvularia penniseti, Curvularia lunata, Fusarium oxysporum f. sp. ciceris and Helminthosporium maydis using poisoned food technique. The DMSO extract of S.anacardium oil was found to be more or less active against almost all tested pathogenic fungi with a varied spectrum of reduced growth. C.lunata has shown 93.3% inhibition and F.oxysporum and H.maydis have shown 94.4% inhibition and 100% mycelial inhibitions at 15% and 18% concentrations of the extract respectively. Whereas, C.penniseti was found to be quite sensitive that showed 88.9 inhibitions at 10% concentration but it showed 100% inhibition at 18% concentration.  


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