Embracing Additive Manufacturing Technology through Fused Filament Fabrication for Antimicrobial with Enhanced Formulated Materials

Antimicrobial materials produced by 3D Printing technology are very beneficial, especially for biomedical applications. Antimicrobial surfaces specifically with enhanced antibacterial property have been prepared using several quaternary salt-based agents, such as quaternary ammonium salts and metallic nanoparticles (NPs), such as copper and zinc, which are incorporated into a polymeric matrix mainly through copolymerization grafting and ionic exchange. This review compared different materials for their effectiveness in providing antimicrobial properties on surfaces. This study will help researchers choose the most suitable method of developing antimicrobial surfaces with the highest efficiency, which can be applied to develop products compatible with 3D Printing Technology.

ISOMERS OF 3-CHLORO-N,N,N-TRIS(3-METHYLBUTYL)PROP-2-EN-1-AMMINIUM CHLORIDE AS COMPLEX OIL AND GAS FIELD REAGENTS WITH ANTIHYDRATE, ANTICORROSIVE AND BACTERICIDAL ACTION

One of the most promising classes of low-dosage hydrate inhibitors is anti-agglomerants, which are favorably characterized by high efficacy at very low working concentrations (0.1-0.5%). We have investigated the possibility of creating new anti-agglomerants with enhanced anticorrosive and bactericidal properties based on the quaternization of tris(3-methylbutyl)amine with (E)- and (Z)-1,3-dichloropropene isomers. It is well known that compounds with a 3-chloroprop-2-enyl fragment have a pronounced anticorrosive and bactericidal action. Thus, the presence in the quaternization products of isopentyl groups and 3-chloroprop-2-enyl fragments that are optimal for preventing agglomeration of the gas hydrates can contribute to the complex antihydrate, anticorrosive and bactericidal activity of these compounds. An attempt to conduct the alkylation of tris(3-methylbutyl)amine with (E)-1,3-dichloropropene in standard solvent – boiling ethanol for 3 days leads to a low yield of the target quaternary salt. Using chromatography-mass spectrometry, it was established that there are significant amounts of by-products in the reaction mixture, which are formed as a result of various nucleophilic substitutions and elimination reactions. Alkylation of tris(3-methylbutyl)amine in boiling acetonitrile proceeds faster and more selectively in 80% yield of (E)-3-chloro-N,N,N-tris(3-methylbutyl)prop-2-en-1-amminium chloride in 20 h. A quaternization with (Z)-1,3-dichlopropene under the same conditions gives an isomeric quaternary salt with a similar yield. The alkylation of tris(3-methylbutyl)amine with isomers of 1,3-dichloropropene proceeds without allyl rearrangement and with full retention of the configuration of the chlorovinyl fragment. The structure and purity of the obtained compounds was unambiguously confirmed by NMR spectroscopy data. Tests in rocking cells using tetrahydrofuran-water model systems (forming the structure sII similar to natural gas hydrates), gravimetric and microbiological methods showed high antihydrate, anticorrosive and bactericidal efficiency of the obtained compounds in concentrations of 0.5%.

Synthesis and anticancer activity of 1-(41-isopropylphenyl)-4-(42-chlorophenyl)5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd]azulene-2-carboxylic acid arylamides against PC-3 prostate cancer cells

Pharmacotherapy of prostate cancer is an important part in combating oncologic diseases. This is very relevant, because prostate cancer is a cause of 10 % of deaths from all cancerous diseases in males. The aim of the study – to synthesize novel derivatives of 1-(41-isopropylphenyl)-4-(42-chlorophenyl)5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd]azulene-2-carboxylic acid arylamides and to evaluate their antitumor activity against PC-3 prostate cancer cells. By reaction of equimolar amounts of 2-methoxy-3,4,5,6-tetrahydro-7H-azepine with a-amino-4-chloroacetophenone chlorohydrate, 3-(4-chlorophenyl)-6,7,8,9- tetrahydro-5Н-imidazo[1,2-a]azepine was synthesized. By alkylation of a-bromo-4-іsopropylacetophenone in ethylacetate and following treatment of the obtained intermediary quaternary salt with excess of 5 % NaOH solution,1-(41-isopropylphenyl)-4-(42chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd] azulene was synthesized. By boiling it with equimolar amounts of correspondding arylisocyanates in dried benzol, an array of 1-(41-iso propylphenyl)-4(42-chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd]azulene-2-carboxylic acid arylamides were synthesized. Structure and purity of all compounds obtained were confirmed by data of MR1Н spectroscopy. Lipophilicity (LogP) of compounds 6 and 8 a-i was calculated with the ACD LogP program. Antitumor activity of 1-(41-isopropylphenyl)-4-(42-chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd]azulene-2-carboxylic acid (3-methylphenyl) and (3-methoxyphenyl)-amides was evaluated at in vitro test on prostate cancer PC-3 cell lines. It is indicated, that at concentration of 10–5 M these compounds exceed 5-fluorouracil as comparison drug in inhibiting PC-3 prostate cancer cells growth by 52.32 % and 3.93 % correspondingly. The data obtained substantiate feasibility of further studies of 1-(41-isopro pylphenyl)-4-(42-chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd] azulene-2-carboxylic acid arylamides as new, potential antitumor medicines for prostate cancer treatment.

Synthesis and anticancer activity of 1-(41-isopropylphenyl)-4-(42-chlorophenyl)5,6,7,8-tetrahydro-2,4a-diazacyclopenta[ cd ]azulene-2-carboxylic acid arylamides against PC-3 prostate cancer cells

Pharmacotherapy of prostate cancer is an important part in combating oncologic diseases. This is very relevant, because prostate cancer is a cause of 10 % of deaths from all cancerous diseases in males. The aim of the study – to synthesize novel derivatives of 1-(41-isopropylphenyl)-4-(42-chlorophenyl)5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd]azulene-2-carboxylic acid arylamides and to evaluate their antitumor activity against PC-3 prostate cancer cells. By reaction of equimolar amounts of 2-methoxy-3,4,5,6-tetrahydro-7H-azepine with a-amino-4-chloroacetophenone chlorohydrate, 3-(4-chlorophenyl)-6,7,8,9- tetrahydro-5Н-imidazo[1,2-a]azepine was synthesized. By alkylation of a-bromo-4-іsopropylacetophenone in ethylacetate and following treatment of the obtained intermediary quaternary salt with excess of 5 % NaOH solution,1-(41-isopropylphenyl)-4-(42chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd] azulene was synthesized. By boiling it with equimolar amounts of correspondding arylisocyanates in dried benzol, an array of 1-(41-iso propylphenyl)-4(42-chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd]azulene-2-carboxylic acid arylamides were synthesized. Structure and purity of all compounds obtained were confirmed by data of MR1Н spectroscopy. Lipophilicity (LogP) of compounds 6 and 8 a-i was calculated with the ACD LogP program. Antitumor activity of 1-(41-isopropylphenyl)-4-(42-chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd]azulene-2-carboxylic acid (3-methylphenyl) and (3-methoxyphenyl)-amides was evaluated at in vitro test on prostate cancer PC-3 cell lines. It is indicated, that at concentration of 10–5 M these compounds exceed 5-fluorouracil as comparison drug in inhibiting PC-3 prostate cancer cells growth by 52.32 % and 3.93 % correspondingly. The data obtained substantiate feasibility of further studies of 1-(41-isopro pylphenyl)-4-(42-chlorophenyl)-5,6,7,8-tetrahydro-2,4а-diazacyclopenta[cd] azulene-2-carboxylic acid arylamides as new, potential antitumor medicines for prostate cancer treatment.

Intensifications of the wooling mechanism with increasing electric conductivity of fibers

The wide possibilities of modifying manufactured industrial fibers aimed at improving their physico-mechanical properties, structural and technological parameters. In connection with the above, it was of interest to study the effect of a number of water-soluble compositions based on a poly-quaternary salt of dimethyl-allyl-β - methacryloyloxyethylammonium bromide in combination with glycerin on the structural and physico-mechanical properties of protein fiber, and also to study the effect of the composition on wool spinning and the quality of wool yarn .

OBTAINING SOME THERMOD AINING SOME THERMODYNAMIC PARAMETERS CONTAINING ME AINING METACRYLATE AND ALL TE AND ALLYL GROUPS CON YL GROUPS CONTAINING IN COMPOSITION

The article discusses the preparation of some thermodynamic parameters characterizing the final product of complex radical polymerization of amino alkyl acrylate derivatives containing both methacrylate and alkyl groups of low molecular weight compounds with electron acceptors - polymerization initiators at temperatures that exclude thermal decomposition of the initiators themselves. The equilibrium constant of the complication reaction and the molar extinction coefficient of the complex were determined by graphically solving the Bеneshe-Hildebrand equation, the heats of complex formation, entropy, Gibbs energy were found, and the elemental composition of low molecular weight and high molecular weight substances was determined. As can be seen from the studies, the molar extinction coefficient of the complex practically does not depend on temperature, and the equilibrium constant of the complexation reaction even in a narrow temperature range (283–293 K) increases with increasing temperature. The structure and composition of the synthesized monomeric and polymer salt were also considered in the work, and confirmed by IR-spectroscopy and analysis of elemental composition, the obtained spectroscopic data showed that the unit of the formed polymer corresponds in composition and structure to the monomeric quaternary salt, and the allyl bond in the polymers is preserved. It can be seen from the studies that, with an increase in the concentration of both the monomer and the initiator, the reaction rate naturally increases.