Water-Based Suspensions of Iron Oxide Nanoparticles with Electrostatic or Steric Stabilization by Chitosan: Fabrication, Characterization and Biocompatibility; Sensors; Vol. 17, iss. 11

ग्रंथसूची विवरण
Parent link:Sensors
Vol. 17, iss. 11.— 2017.— [20 p.]
निगमित लेखकों: Национальный исследовательский Томский политехнический университет (ТПУ) Институт природных ресурсов (ИПР) Кафедра физической и аналитической химии (ФАХ), Национальный исследовательский Томский политехнический университет (ТПУ) Физико-технический институт (ФТИ) Кафедра экспериментальной физики (ЭФ)
अन्य लेखक: Kurlyandskaya G. V. Galina Vladimirovna, Litvinova L. S. Larisa, Safronov A. P. Alexander Petrovich, Shupletsova V. V. Valeria, Tyukova I. S. Irina, Khaziakhmatova O. G. Olga Gennadjevna, Slepchenko G. B. Galina Borisovna, Yurova K. A. Kristina, Cherempey E. G. Elena Gennadjevna, Kulesh N. A. Nikita Aleksandrovich, Andrade R. Ricardo, Beketov I. V. Igor, Khlusov I. A. Igor Albertovich
सारांश:Title screen
Present day biomedical applications, including magnetic biosensing, demand better understanding of the interactions between living systems and magnetic nanoparticles (MNPs). In this work spherical MNPs of maghemite were obtained by a highly productive laser target evaporation technique. XRD analysis confirmed the inverse spinel structure of the MNPs (space group Fd-3m). The ensemble obeyed a lognormal size distribution with the median value 26.8 nm and dispersion 0.362. Stabilized water-based suspensions were fabricated using electrostatic or steric stabilization by the natural polymer chitosan. The encapsulation of the MNPs by chitosan makes them resistant to the unfavorable factors for colloidal stability typically present in physiological conditions such as pH and high ionic force. Controlled amounts of suspensions were used for in vitro experiments with human blood mononuclear leukocytes (HBMLs) in order to study their morphofunctional response. For sake of comparison the results obtained in the present study were analyzed together with our previous results of the study of similar suspensions with human mesenchymal stem cells. Suspensions with and without chitosan enhanced the secretion of cytokines by a 24-h culture of HBMLs compared to a control without MNPs. At a dose of 2.3, the MTD of chitosan promotes the stimulating effect of MNPs on cells. In the dose range of MNPs 10–1000 MTD, chitosan “inhibits” cellular secretory activity compared to MNPs without chitosan. Both suspensions did not caused cell death by necrosis, hence, the secretion of cytokines is due to the enhancement of the functional activity of HBMLs. Increased accumulation of MNP with chitosan in the cell fraction at 100 MTD for 24 h exposure, may be due to fixation of chitosan on the outer membrane of HBMLs. The discussed results can be used for an addressed design of cell delivery/removal incorporating multiple activities because of cell capability to avoid phagocytosis by immune cells.
भाषा:अंग्रेज़ी
प्रकाशित: 2017
विषय:
ऑनलाइन पहुंच:http://dx.doi.org/10.3390/s17112605
स्वरूप: इलेक्ट्रोनिक पुस्तक अध्याय
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=656831

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200 1 |a Water-Based Suspensions of Iron Oxide Nanoparticles with Electrostatic or Steric Stabilization by Chitosan: Fabrication, Characterization and Biocompatibility  |f G. V. Kurlyandskaya [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 44 tit.] 
330 |a Present day biomedical applications, including magnetic biosensing, demand better understanding of the interactions between living systems and magnetic nanoparticles (MNPs). In this work spherical MNPs of maghemite were obtained by a highly productive laser target evaporation technique. XRD analysis confirmed the inverse spinel structure of the MNPs (space group Fd-3m). The ensemble obeyed a lognormal size distribution with the median value 26.8 nm and dispersion 0.362. Stabilized water-based suspensions were fabricated using electrostatic or steric stabilization by the natural polymer chitosan. The encapsulation of the MNPs by chitosan makes them resistant to the unfavorable factors for colloidal stability typically present in physiological conditions such as pH and high ionic force. Controlled amounts of suspensions were used for in vitro experiments with human blood mononuclear leukocytes (HBMLs) in order to study their morphofunctional response. For sake of comparison the results obtained in the present study were analyzed together with our previous results of the study of similar suspensions with human mesenchymal stem cells. Suspensions with and without chitosan enhanced the secretion of cytokines by a 24-h culture of HBMLs compared to a control without MNPs. At a dose of 2.3, the MTD of chitosan promotes the stimulating effect of MNPs on cells. In the dose range of MNPs 10–1000 MTD, chitosan “inhibits” cellular secretory activity compared to MNPs without chitosan. Both suspensions did not caused cell death by necrosis, hence, the secretion of cytokines is due to the enhancement of the functional activity of HBMLs. Increased accumulation of MNP with chitosan in the cell fraction at 100 MTD for 24 h exposure, may be due to fixation of chitosan on the outer membrane of HBMLs. The discussed results can be used for an addressed design of cell delivery/removal incorporating multiple activities because of cell capability to avoid phagocytosis by immune cells. 
461 |t Sensors 
463 |t Vol. 17, iss. 11  |v [20 p.]  |d 2017 
610 1 |a труды учёных ТПУ 
610 1 |a электронный ресурс 
610 1 |a magnetic biosensors 
610 1 |a iron oxide magnetic nanoparticles 
610 1 |a chitosan 
610 1 |a ferrofluids 
610 1 |a human blood mononuclear leukocytes 
610 1 |a morphofunctional response 
610 1 |a магнитные биосенсоры 
610 1 |a магнитные наночастицы 
610 1 |a оксид железа 
610 1 |a хитозан 
610 1 |a феррожидкости 
610 1 |a мононуклеарные лейкоциты 
610 1 |a человек 
610 1 |a кровь 
701 1 |a Kurlyandskaya  |b G. V.  |g Galina Vladimirovna 
701 1 |a Litvinova  |b L. S.  |g Larisa 
701 1 |a Safronov  |b A. P.  |g Alexander Petrovich 
701 1 |a Shupletsova  |b V. V.  |g Valeria 
701 1 |a Tyukova  |b I. S.  |g Irina 
701 1 |a Khaziakhmatova  |b O. G.  |g Olga Gennadjevna 
701 1 |a Slepchenko  |b G. B.  |c Chemist  |c Professor of Tomsk Polytechnic University, Doctor of chemical sciences  |f 1956-  |g Galina Borisovna  |3 (RuTPU)RU\TPU\pers\33018  |9 16858 
701 1 |a Yurova  |b K. A.  |g Kristina 
701 1 |a Cherempey  |b E. G.  |g Elena Gennadjevna 
701 1 |a Kulesh  |b N. A.  |g Nikita Aleksandrovich 
701 1 |a Andrade  |b R.  |g Ricardo 
701 1 |a Beketov  |b I. V.  |g Igor 
701 1 |a Khlusov  |b I. A.  |c biophysicist  |c Professor of Tomsk Polytechnic University, doctor of medical Sciences  |f 1963-  |g Igor Albertovich  |3 (RuTPU)RU\TPU\pers\34907  |9 18225 
712 0 2 |a Национальный исследовательский Томский политехнический университет (ТПУ)  |b Институт природных ресурсов (ИПР)  |b Кафедра физической и аналитической химии (ФАХ)  |3 (RuTPU)RU\TPU\col\18656 
712 0 2 |a Национальный исследовательский Томский политехнический университет (ТПУ)  |b Физико-технический институт (ФТИ)  |b Кафедра экспериментальной физики (ЭФ)  |3 (RuTPU)RU\TPU\col\21255 
801 2 |a RU  |b 63413507  |c 20171214  |g PSBO 
856 4 |u http://dx.doi.org/10.3390/s17112605 
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