candida pseudotropicalis
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2021 ◽  
Vol 22 (1) ◽  
pp. 74-87
Author(s):  
A.O. Oyedele ◽  
E.O. Akinkunmi

Background: Benzoic acid (BA) and salicylic acid (SA) combined are used as choice topical treatment for fungal and bacterial infections but their delivery is affected by ointment vehicle, among other factors. With aim to achieve improved release and antimicrobial activity in ointment formulation of these medicaments through selection of more efficient vehicle(s), this study comparatively evaluated prospective alternatives to thecompendium-specified base for delivery potential and relevant physical properties.Methodology: Water-sorption capacity, rheological characteristics and heat-tolerance limits of six hydrophilic bases [hydrous ointment (HO), hydrous sheabutter (HS), neat sheabutter (NS), lanolin anhydrous (LA), lanolin hydrous (LH), and emulsifying ointment (EO)] and their ointment products containing 1, 2, 3, or 6% w/w of BA or SA were determined. Drug delivery propensity of the products was evaluated by agar diffusion colorimetric assay, while their antimicrobial activities were determined by hole-in-plate agar diffusion assay against selected type organisms (Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Candida albicans and Candida pseudotropicalis).Results: BA was released in relatively larger quantity and demonstrated greater antimicrobial activity than SA in most bases. The released quantities of each medicament correlated directly with concentration and antimicrobial activities. The rates and extents of drug release followed a similar trend in different vehicles namely, HO > HS > NS ≥ EO > LA ≈ LH. Water number of base, ointment preparation method, viscosity, or heat-tolerance showed no influence on drug release or antimicrobial activity.Conclusion: HO and HS are better vehicles for delivery of BA and SA in ointment than EO which is the prototypical base. Keywords: Benzoic acid, Salicylic acid, Antimicrobial activity, Ointment base, Delivery factors French Title: Évaluation comparative des bases hydrophiles pour une meilleure administration d'acide benzoïque et d'acide salicylique dans une pommade antimicrobienne Contexte: L'acide benzoïque (BA) et l'acide salicylique (SA) combinés sont utilisés comme traitement topique de choix pour les infections fongiques et bactériennes, mais leur administration est affectée par le véhicule de la pommade, entre autres facteurs. Dans le but d'améliorer la libération et l'activité antimicrobienne dans la  formulation de pommade de ces médicaments grâce à la sélection de véhicules plus efficaces, cette étude a évalué comparativement des alternatives potentielles à la base spécifiée dans le compendium pour le potentiel d'administration et les propriétés physiques pertinentes.Méthodologie: Capacité de sorption de l'eau, caractéristiques rhéologiques et limites de tolérance à la chaleur de six bases hydrophiles [pommade hydratée (HO), beurre de karité hydraté (HS), beurre de karité pur (NS), lanoline anhydre (LA), lanoline hydratée (LH), et onguent émulsifiant (EO)] et leurs produits de pommade contenant 1, 2, 3 ou 6% p/p de BA ou SA ont été déterminés. La propension à l'administration de médicaments des produits a été évaluée par un essai colorimétrique de diffusion sur gélose, tandis que leurs activités antimicrobiennes ont été déterminées par un essai de diffusion sur gélose en plaque contre des organismes de type sélectionné (Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Candida albicans et Candida pseudotropicalis).Résultats: BA a été libéré en quantité relativement plus grande et a démontré une plus grande activité antimicrobienne que SA dans la plupart des bases. Les quantités libérées de chaque médicament étaient directement liées à la concentration et aux activités antimicrobiennes. Les taux et l'étendue de la libération de médicaments ont suivi une tendance similaire dans différents véhicules, à savoir HO> HS> NS ≥ EO> LA ≈ LH. Le nombre d'eau de base, la méthode de préparation de la pommade, la viscosité ou la tolérance à la chaleur n'ont montré aucune influence sur la libération du médicament ou l'activité antimicrobienne.Conclusion: HO et HS sont de meilleurs véhicules pour la livraison de BA et SA en onguent que EO qui est la base prototypique. Mots-clés: acide benzoïque, acide salicylique, activité antimicrobienne, base de pommade, facteurs de délivrance  


2019 ◽  
Vol 4 (3) ◽  
pp. 1-4
Author(s):  
Shoaib M

Due to increasing antimicrobial resistance, functionally substituted cyclohexane derivatives are being explored as potential antimicrobial agents. Reaction of diethyl 4 - hydroxy - 6 - (hyd - roxyimino) - 4 - methyl - 2 - phenylcyclohexane - 1,3 - dicarboxylate with 4 - toluene sulfonyl chloride in boiling acetone in the presence of equimolar triethylamine resulted in formation of diethyl - 4 - hydroxy - 4 - methyl - 2 - phenyl - 6 - ((tosyloxy)imino) cyclohexane - 1,3 - dicarboxylate. The structure of novel compound was characterized by 1 H and 13 C NMR spectra and elemental analysis was performed. Agar well diffusion assay was used to screen novel compound against Gram - positive bacteria, Gram - negative bacteria and fungi. Test compound showed better antimicrobial properties against Gram - negative bac teria as compared to Gram - positive bacteria and fungi. Acinetobacter baumannii BDU - 32 was found to be most sensitive bacteria while Candida pseudotropicalis BDU MA88 was found to be most sensitive yeast.


2008 ◽  
Vol 43 (3) ◽  
pp. 284-288 ◽  
Author(s):  
Ts. Hristozova ◽  
V. Gotcheva ◽  
B. Tzvetkova ◽  
D. Paskaleva ◽  
A. Angelov

2005 ◽  
pp. 231-238 ◽  
Author(s):  
Sanja Podunavac-Kuzmanovic ◽  
Dragoljub Cvetkovic ◽  
Gordana Cetkovic

Zinc(II) chloride reacts with 2-methylbenzimidazole derivatives to give complexes of the formula ZnL2Cl2-nH2O, where L=2-methylbenzimidazole l-benzyl-2-methylbenzimida-zole and l-(4-methylbenzyl)-2-methylbenzimidazole n=0, 0.5 or 1. All the ligands and their zinc(II) complexes were evaluated for their in vitro antimicrobial activity against Pseudomonas aeruginosa Bacillus sp., Staphylococcus aureus, Sarcina lutea and Candida pseudotropicalis. It was found that the majority of the investigated compounds displayed in vitro antimicrobial activity against very persistent microorganisms, except for the starting ligand, 2-methylbenzimidazole and its zinc(II) complex which were active only against gram-negative bacteria. None of the compounds was significantly effective against Candida pseudotropicalis, except for l-(4-methylbenzyl)-2-methylbenzimidazoleandits complex, which very slightly or slightly inhibited the yeast growth. The minimum inhibitory concentration (MIC) was determined for all the ligands and their complexes. The effect of ligand and complex structure on the antimicrobial activity was discussed.


2003 ◽  
Vol 58 (5-6) ◽  
pp. 381-385 ◽  
Author(s):  
Svetla Vassileva ◽  
Bonka Tzvetkova

Abstract The studied problem is of commercial interest because whey, the cultivation substrate, is a waste by-product from the transformation of milk into cheese and casein. Investigations on the influence of the dilution rate (D) on the bioproductivity of lactose-utilizing yeasts were carried out with two model strains D the oxidative strain Candida blankii 35 and the fermentative strain Candida pseudotropicalis 11. The increase of D led to the different changes in productivity. The best synthesizing ability of both continuously cultivated strains is established at D = 0.4 [h-1] despite the different type of metabolism. The oxidative strain C. blankii 35 is more effective in comparison with the fermentative strain C. pseudotropicalis 11 because of its ability to synthesize 1.5 fold higher biomass and protein yields. These experimental facts were proved also by simulative research with a Fuzzy Knowledge-Based System (FKBS) developed for modeling the influence of D on several process variables.


1999 ◽  
Vol 13 (2) ◽  
pp. 119-121
Author(s):  
Ch. Katranushkova ◽  
B. Tzvetkova ◽  
L. Losseva ◽  
Ts. Hristozova ◽  
V. Gancheva

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