Biological activity of carbonic nano-structures—comparison via enzymatic bioassay; Journal of Soils and Sediments; Vol. 19

Bibliografske podrobnosti
Parent link:Journal of Soils and Sediments.— : Springer-Verlag GmbH Germany
Vol. 19.— 2019.— P. 2689-2696
Drugi avtorji: Sachkova A. S. Anna Sergeevna, Kovel E. S. Ekaterina Sergeevna, Churilov G. N. Grigory Nikolaevich, Stom D. I. Devard Iosifovich, Kudryasheva N. S. Nadezhda Stepanovna
Izvleček:Title screen
Purpose The aim of the work is to compare the biological activity of carbonic nano-structures of natural and artificial origination, namely, humic substances (HS) and fullerenols. Materials and methods The representative of the fullerenol group, С60Оy(OH)x where у + x = 20-22, was chosen. Enzyme-based luminescent bioassay was applied to evaluate toxicity and antioxidant properties of HS and fullerenol (F); chemiluminescent luminol method was used to study a content of reactive oxygen species (ROS) in the solutions. Toxicity of the bioactive compounds was evaluated using effective concentrations ЕС50; detoxification coefficients DOxT were applied to study and compare antioxidant activity of the compounds. Antioxidant activity and ranges of active concentrations of the bioactive compounds were determined in model solutions of organic and inorganic oxidizers-1,4-benzoquinone and potassium ferricianide.
Results and discussion Values of ЕС50 revealed higher toxicity of HS than F (0.005 and 0.108 g L−1 , respectively); detoxifying concentrations of F were found to be lower. Antioxidant ability of HS was demonstrated to be time-dependent; the 50-min preliminary incubation in oxidizer solutions was suggested as optimal for the detoxification procedure. On the contrary, F' antioxidant effect demonstrated independency on time. Antioxidant effect of HS did not depend on amphiphilic characteristics of the media (values of DOxTwere 1.3 in the solutions of organic and inorganic oxidizers), while this of F was found to depend: it was maximal (DOxT = 2.0) in solutions of organic oxidizer, 1,4-benzoquinone. Conclusions Both HS and F demonstrated toxicity and low-concentration antioxidant ability; however, quantitative characteristics of their effects were different. The differences were explained with HS polyfunctionality, higher ability to decrease ROS content, non-rigidity, and diffusion restrictions in their solutions. Antioxidant effect of the bioactive compounds was presumably attributed to catalytic redox activity of their π-fragments. The paper demonstrates a high potential of luminescent enzymatic bioassay to study biological activity of nano-structures of natural and artificial origination
AM_Agreement
Jezik:angleščina
Izdano: 2019
Teme:
Online dostop:https://doi.org/10.1007/s11368-018-2134-9
Format: Elektronski Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=659728

MARC

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200 1 |a Biological activity of carbonic nano-structures—comparison via enzymatic bioassay  |f Anna S. Sachkova, Ekaterina S. Kovel, Grigoriy N. Churilov [et al.] 
203 |a Текст  |c электронный  |b визуальный 
300 |a Title screen 
330 |a Purpose The aim of the work is to compare the biological activity of carbonic nano-structures of natural and artificial origination, namely, humic substances (HS) and fullerenols. Materials and methods The representative of the fullerenol group, С60Оy(OH)x where у + x = 20-22, was chosen. Enzyme-based luminescent bioassay was applied to evaluate toxicity and antioxidant properties of HS and fullerenol (F); chemiluminescent luminol method was used to study a content of reactive oxygen species (ROS) in the solutions. Toxicity of the bioactive compounds was evaluated using effective concentrations ЕС50; detoxification coefficients DOxT were applied to study and compare antioxidant activity of the compounds. Antioxidant activity and ranges of active concentrations of the bioactive compounds were determined in model solutions of organic and inorganic oxidizers-1,4-benzoquinone and potassium ferricianide. 
330 |a Results and discussion Values of ЕС50 revealed higher toxicity of HS than F (0.005 and 0.108 g L−1 , respectively); detoxifying concentrations of F were found to be lower. Antioxidant ability of HS was demonstrated to be time-dependent; the 50-min preliminary incubation in oxidizer solutions was suggested as optimal for the detoxification procedure. On the contrary, F' antioxidant effect demonstrated independency on time. Antioxidant effect of HS did not depend on amphiphilic characteristics of the media (values of DOxTwere 1.3 in the solutions of organic and inorganic oxidizers), while this of F was found to depend: it was maximal (DOxT = 2.0) in solutions of organic oxidizer, 1,4-benzoquinone. Conclusions Both HS and F demonstrated toxicity and low-concentration antioxidant ability; however, quantitative characteristics of their effects were different. The differences were explained with HS polyfunctionality, higher ability to decrease ROS content, non-rigidity, and diffusion restrictions in their solutions. Antioxidant effect of the bioactive compounds was presumably attributed to catalytic redox activity of their π-fragments. The paper demonstrates a high potential of luminescent enzymatic bioassay to study biological activity of nano-structures of natural and artificial origination 
371 0 |a AM_Agreement 
461 1 |t Journal of Soils and Sediments  |n Springer-Verlag GmbH Germany 
463 1 |t Vol. 19  |v P. 2689-2696  |d 2019 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a antioxidant activity 
610 1 |a bioactive compounds 
610 1 |a fullerenol humic substances 
610 1 |a toxicity 
610 1 |a reactive oxygen species 
610 1 |a антиоксидантная активность 
610 1 |a биологически активные соединения 
610 1 |a фуллеренолы 
610 1 |a гуминовые вещества 
610 1 |a токсичность 
610 1 |a активный кислород 
701 1 |a Sachkova  |b A. S.  |c biologist  |c Associate Professor of Tomsk Polytechnic University, candidate of biological sciences  |f 1986-  |g Anna Sergeevna  |3 (RuTPU)RU\TPU\pers\36753  |9 19792 
701 1 |a Kovel  |b E. S.  |g Ekaterina Sergeevna 
701 1 |a Churilov  |b G. N.  |g Grigory Nikolaevich 
701 1 |a Stom  |b D. I.  |g Devard Iosifovich 
701 1 |a Kudryasheva  |b N. S.  |g Nadezhda Stepanovna 
801 2 |a RU  |b 63413507  |c 20190326  |g RCR 
856 4 |u https://doi.org/10.1007/s11368-018-2134-9 
942 |c CF