SYNTHESIS AND STUDY OF THE ANTIMICROBIAL ACTIVITY OF POLYHEXAMETHYLENE GUANIDINE HYDROCHLORIDE DERIVATIVES

Author(s):  
S. Stelmakh ◽  
M. Grigor’eva ◽  
N. Garkusheva ◽  
D. Mognonov ◽  
V. Batoev

N-phenyl- and N-octyl-substituted derivatives of polyhexamethylene guanidine hydrochloride were synthesized and their antimicrobial activity against nosocomial infections was determined.

2012 ◽  
Vol 61 (10) ◽  
pp. 1421-1427 ◽  
Author(s):  
Mathias K. Oulé ◽  
Kelsi Quinn ◽  
Michael Dickman ◽  
Anne-Marie Bernier ◽  
Sylvie Rondeau ◽  
...  

Author(s):  
O. Ochirov ◽  
E. Burasova ◽  
S. Stelmakh ◽  
M. Grigor'eva ◽  
V. Okladnikova ◽  
...  

The resistance of bacteria to the disinfectants used is one of the pressing health problems that need to be addressed in order to prevent the formation and spread of resistant strains. This leads to a sharp decrease in the effectiveness of anti-epidemic measures and contributes to maintaining a high level of morbidity. In the context of the growing incidence of HAIs, their polyetiology, the large adaptive potential of opportunistic microorganisms, and the growing resistance to antimicrobial drugs, it is necessary to search for new or modify the corresponding substances of plant or synthetic origin that have antimicrobial action and are used as antimicrobial agents. One of the representatives of this class of compounds are polyguanidines, characterized by high antimicrobial activity and low toxicity. Due to the high reactivity of the guanidine group, as well as the ease of synthesis and the relative availability of raw materials, N-phenyl- and N-octyl-substituted derivatives of polyhexamethylene guanidine hydrochloride were obtained by melt polycondensation, their molecular weight characteristics were determined, and the structure was investigated by IR spectroscopy. An earlier study of the acute toxicity of polyhexamethylene guanidine hydrochloride derivatives after a single oral intake of drugs into the body of laboratory animals (white mice) made it possible to establish the following LD50 values: polyhexamethylene guanidine hydrochloride - 850.0 ± 112.02 mg / kg; N-phenyl-substituted polyhexamethylene guanidine hydrochloride - 1399.9 ± 120.51 mg / kg; N-octyl-substituted polyhexamethylene guanidine hydrochloride - 1150.0 ± 137.40 mg / kg. The obtained values, according to the tabulation of hazard classes, allow the synthesized derivatives to be classified into the fourth hazard class and open up the possibility of using disinfectants as active components. The evaluation of the antibacterial properties of the samples was carried out by the method of serial dilutions in agar on hospital strains of bacteria and fungi isolated from the biomaterial of patients of the Republican Clinical Hospital named after N.A. Semashko, according to the clinical guidelines "Laboratory diagnosis of community-acquired pneumonia" 2014; "Bacteriological analysis of urine" 2014; "Determination of the susceptibility of microorganisms to antimicrobial drugs" 2015 It was found that N-substituted derivatives exhibit a greater antimicrobial effect in comparison with an unsubstituted polymer. The most sensitive to all the drugs presented are the yeast-like fungi Candida albicans (No. 2495) (complete suppression), as well as methicillin-resistant St. aureus (no. 2544), and the substituted samples almost completely suppress its growth. The most resistant strains are P. aeruginosa (No. 2281), A. Baumannii (No. 2806) and K. Pneumoniae (No. 3023), the percentage of reduction of these bacteria under the action of substituted samples does not exceed 41%, which is explained by their multi-resistance.


2018 ◽  
Vol 11 (2) ◽  
pp. 164-172
Author(s):  
О.A. Yessimova ◽  
◽  
А.О. Adilbekova ◽  
M.Zh. Kerimkulova ◽  
G.D. Isenova ◽  
...  

2020 ◽  
Vol 17 (2) ◽  
pp. 214-225 ◽  
Author(s):  
Piotr Kawczak ◽  
Leszek Bober ◽  
Tomasz Bączek

Background: Nitro-derivatives of heterocyclic compounds were used as active agents against pathogenic microorganisms. A set of 4- and 5-nitroimidazole derivatives exhibiting antimicrobial activity was analyzed with the use of Quantitative Structure-Activity Relationships (QSAR) method. The study included compounds used both in documented treatment and those described as experimental. Objective: The purpose of this study was to demonstrate the common and differentiating characteristics of the above-mentioned chemical compounds alike physicochemically as well as pharmacologically based on the quantum chemical calculations and microbiological activity data. Methods: During the study PCA and MLR analysis were performed, as the types of proposed chemometric approach. The semi-empirical and ab initio level of in silico molecular modeling was performed for calculations of molecular descriptors. Results: QSAR models were proposed based on chosen descriptors. The relationship between the nitro-derivatives structure and microbiological activity data was able to class and describe the antimicrobial activity with the use of statistically significant molecular descriptors. Conclusion: The applied chemometric approaches revealed the influential features of the tested structures responsible for the antimicrobial activity of studied nitro-derivatives.


2021 ◽  
Vol 11 (3) ◽  
pp. 1180
Author(s):  
Kinga Paruch ◽  
Łukasz Popiołek ◽  
Anna Biernasiuk ◽  
Anna Berecka-Rycerz ◽  
Anna Malm ◽  
...  

Bacterial infections, especially those caused by strains resistant to commonly used antibiotics and chemotherapeutics, are still a current threat to public health. Therefore, the search for new molecules with potential antimicrobial activity is an important research goal. In this article, we present the synthesis and evaluation of the in vitro antimicrobial activity of a series of 15 new derivatives of 4-methyl-1,2,3-thiadiazole-5-carboxylic acid. The potential antimicrobial effect of the new compounds was observed mainly against Gram-positive bacteria. Compound 15, with the 5-nitro-2-furoyl moiety, showed the highest bioactivity: minimum inhibitory concentration (MIC) = 1.95–15.62 µg/mL and minimum bactericidal concentration (MBC)/MIC = 1–4 µg/mL.


2008 ◽  
Vol 74 (3) ◽  
pp. 566-571 ◽  
Author(s):  
Már Másson ◽  
Jukka Holappa ◽  
Martha Hjálmarsdóttir ◽  
Ögmundur V. Rúnarsson ◽  
Tapio Nevalainen ◽  
...  

2012 ◽  
Vol 77 (1) ◽  
pp. 17-26 ◽  
Author(s):  
Ritu Sharma ◽  
Pushkal Samadhiya ◽  
Savitri Srivastava ◽  
Santosh Srivastava

A new series of N-[3-(10H-phenothiazinyl)-propyl]-2-(substituted phenyl)-4-oxo-5-( substituted benzylidene)-1,3-thiazolidine-carboxamide, 5(as) have been synthesized. The cycloaddition reaction of thioglycolic acid with N-[3-(10H-phenothiazinyl)-propyl]-N?-[(substituted phenyl)-methylidene]- urea, 3(a-s) in the presence of anhydrous ZnCl2 afforded new heterocyclic compounds N-[3-(10H-phenothiazinyl)-propyl]-2-(substituted phenyl)-4-oxo- 1,3-thiazolidine-carboxamide, 4(a-s). The later product on treatment with several selected substituted aromatic aldehydes in the presence of C2H5ONa undergoes Knoevenagel reaction to yield 5(a-s). The structure of compounds 1, 2, 3(a-s), 4(a-s) and 5(a-s) were confirmed by IR, 1H NMR, 13C NMR, Fmass and chemical analysis. All above compounds were screened for their antimicrobial activity against some selected bacteria and fungi and for antituberculosis activity compounds have been screened against the bacterium M. tuberculosis.


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