Javascript must be enabled to continue!
Antimicrobial properties of newly synthesised aryl acyclic amino alcohols against clinical strains of enterococci
View through CrossRef
Objective. The present work is devoted to the in vitro antimicrobial activity of newly synthesized aryl acyclic amino alcohols, namely, derivatives of alkyl (R-aryl) oxydialkyl ammonium salts against clinical strains of enterococci.
Materials and methods. The object of the study was 52 newly synthesized aryl acyclic amino alcohols, namely derivatives of quaternary salts of alkyl(aryloxyethoxy)dialkylaminopropanol, synthesized at the Institute of Organic Chemistry of the National Academy of Sciences of Ukraine. The antimicrobial activity was evaluated in vitro by agar diffusion and serial dilutions against the reference strain Enterococcus faecalis ATCC 29212 and 25 clinical isolates. The efficacy of the compounds against clinical strains was evaluated by comparison with the activity of antimicrobial drugs.
Results. As a result of the screening against the reference strain, the compounds with the most pronounced antienterococcal activity were identified. The most active ones (Kc21, Kc14, Kc28, Kc13, Kp13) had retention zones of more than 14 mm. The MIC determination identified 10 most active compounds, the MIC of Kp10 and Kp19 against the reference strain was 0.58 ± 0.10 μg/ml and 1.76 ± 0.19 μg/ml. As for clinical strains, the compounds showed moderate activity, with MIC values ranging from 0.48 to 15.63 μg/ml, inhibiting a proportion of isolates at the level of ampicillin and vancomycin. All compounds outperformed the activity of tetracycline in inhibiting antibiotic-resistant strains. The antimicrobial effect of the studied substances was at the level of decamethoxin and significantly exceeded the activity of miramistin.
Conclusions. The study made it possible to identify the 10 most active compounds against the test microorganisms and to compare them with commercial antimicrobial drugs. The list of the most effective aryl acyclic amino alcohols is presented in the following list: Kp10, Kp19, Kp8, Kc2, Kp18, Kc23 Kc1, Kc3, Kc4, and Kc22. The data obtained indicate the prospects for further study of the antimicrobial properties of alkyl (R-aryl) oxydialkyl ammonium derivatives
Title: Antimicrobial properties of newly synthesised aryl acyclic amino alcohols against clinical strains of enterococci
Description:
Objective.
The present work is devoted to the in vitro antimicrobial activity of newly synthesized aryl acyclic amino alcohols, namely, derivatives of alkyl (R-aryl) oxydialkyl ammonium salts against clinical strains of enterococci.
Materials and methods.
The object of the study was 52 newly synthesized aryl acyclic amino alcohols, namely derivatives of quaternary salts of alkyl(aryloxyethoxy)dialkylaminopropanol, synthesized at the Institute of Organic Chemistry of the National Academy of Sciences of Ukraine.
The antimicrobial activity was evaluated in vitro by agar diffusion and serial dilutions against the reference strain Enterococcus faecalis ATCC 29212 and 25 clinical isolates.
The efficacy of the compounds against clinical strains was evaluated by comparison with the activity of antimicrobial drugs.
Results.
As a result of the screening against the reference strain, the compounds with the most pronounced antienterococcal activity were identified.
The most active ones (Kc21, Kc14, Kc28, Kc13, Kp13) had retention zones of more than 14 mm.
The MIC determination identified 10 most active compounds, the MIC of Kp10 and Kp19 against the reference strain was 0.
58 ± 0.
10 μg/ml and 1.
76 ± 0.
19 μg/ml.
As for clinical strains, the compounds showed moderate activity, with MIC values ranging from 0.
48 to 15.
63 μg/ml, inhibiting a proportion of isolates at the level of ampicillin and vancomycin.
All compounds outperformed the activity of tetracycline in inhibiting antibiotic-resistant strains.
The antimicrobial effect of the studied substances was at the level of decamethoxin and significantly exceeded the activity of miramistin.
Conclusions.
The study made it possible to identify the 10 most active compounds against the test microorganisms and to compare them with commercial antimicrobial drugs.
The list of the most effective aryl acyclic amino alcohols is presented in the following list: Kp10, Kp19, Kp8, Kc2, Kp18, Kc23 Kc1, Kc3, Kc4, and Kc22.
The data obtained indicate the prospects for further study of the antimicrobial properties of alkyl (R-aryl) oxydialkyl ammonium derivatives.
Related Results
Amino Acids, Survey
Amino Acids, Survey
AbstractAmino acids are the main components of proteins. Approximately 20 amino acids are common constituents of proteins and are called protein amino acids, or primary protein ami...
Amino Acids
Amino Acids
AbstractAmino acids are the main components of proteins. Approximately 20 amino acids are common constituents of proteins and are called protein amino acids, or primary protein ami...
Vancomycin resistant enterococci gut Colonization and its associated factors among HIV infected patients on anti-Retro viral therapy in Ethiopia
Vancomycin resistant enterococci gut Colonization and its associated factors among HIV infected patients on anti-Retro viral therapy in Ethiopia
Abstract
BackgroundThe emergence of vancomycin resistant Enterococci (VRE) has alarmed the global infectious diseases community due to its tendency for colonization of the ...
MAGNITUDE OF VANCOMYCIN RESISTANT ENTEROCOCCUS FECAL COLONIZATION AND BACTEREMIA IN PATIENTS WITH HEMATOLOGICAL DISEASES AT TERTIARY BONE MARROW TRANSPLANT CENTRE RAWALPINDI
MAGNITUDE OF VANCOMYCIN RESISTANT ENTEROCOCCUS FECAL COLONIZATION AND BACTEREMIA IN PATIENTS WITH HEMATOLOGICAL DISEASES AT TERTIARY BONE MARROW TRANSPLANT CENTRE RAWALPINDI
Objective: To discover the frequency of vancomycin resistant enterococci (VRE) fecal colonization and subsequent bacteremia in patients with hematological diseases in a bone marrow...
Diversity of VanA Glycopeptide Resistance Elements in Enterococci from Humans and Nonhuman Sources
Diversity of VanA Glycopeptide Resistance Elements in Enterococci from Humans and Nonhuman Sources
ABSTRACT
Elements mediating VanA glycopeptide resistance in 106 diverse enterococci from humans and nonhuman sources were compared with the prototype VanA tr...
High Gastrointestinal Colonization Rate of Vancomycin‐Resistant Enterococci among Hospitalized Patients: Potential Source for Resistant Gene
High Gastrointestinal Colonization Rate of Vancomycin‐Resistant Enterococci among Hospitalized Patients: Potential Source for Resistant Gene
Background. Vancomycin‐resistant Enterococci (VRE) is a global health problem and responsible for healthcare‐associated infections (HAIs) in patients with prolonged hospital stay, ...
Cytoplasmic amino acid profiles of clinical and ATCC 29213 strains of Staphylococcus aureus harvested at different growth phases
Cytoplasmic amino acid profiles of clinical and ATCC 29213 strains of Staphylococcus aureus harvested at different growth phases
Staphylococcus aureus strains are a great contributor to both hospital acquired infections as well as community acquired infections. The objective of the present investigation was ...
GLYCOPEPTIDE SUSCEPTIBILITY AMONG STAPHYLOCOCCI AND ENTEROCOCCI ISOLATES FROM SULAIMANI HEALTH LABORATORIES
GLYCOPEPTIDE SUSCEPTIBILITY AMONG STAPHYLOCOCCI AND ENTEROCOCCI ISOLATES FROM SULAIMANI HEALTH LABORATORIES
Background
Glycopeptide antibiotics are bactericidal agents that inhibit late stage bacterial cell wall peptidoglycan synthesis in Gram-positive bacteria. They are used for multir...

