Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/75478
Title: The use of manganese-doped mesoporous silica nanopowder for targeted drug delivery
Authors: Zlygosteva, O. A.
Sokovnin, Y. S.
Ilves, V. G.
Issue Date: 2018
Publisher: Institute of Physics Publishing
Citation: Zlygosteva O. A. The use of manganese-doped mesoporous silica nanopowder for targeted drug delivery / O. A. Zlygosteva, Y. S. Sokovnin, V. G. Ilves // Journal of Physics: Conference Series. — 2018. — Vol. 1115. — Iss. 4. — 42067.
Abstract: The researched manganese-doped mesoporous silica nanopowder (SiO 2 -MnO 2 NP) was produced using evaporation caused by a pulsed electron beam in a vacuum. The synthesized material demonstrated high porosity, amorphous structure and magnetic properties increased with the addition of dopant. The evaluation of the sedimentation stability of NP suspensions showed the need for the additional stabilization. It was established that increasing the sonication time, as the way to increase stability, leads to changes in the structure of the NP. PEG stabilized suspensions showed the highest stability. Experimental results indicated that for different drugs individual methods of loading and release are required. Drug loaded NP demonstrated a high drug loading capacity of 0.09 mg Amoxicillin per mg NP, 0.075 mg Doxorubicin per mg NP that is five times higher than loading capacity of chemically synthesized NP. © Published under licence by IOP Publishing Ltd.
Keywords: CONTROLLED DRUG DELIVERY
FLUXES
LOADING
MANGANESE
MANGANESE OXIDE
NANOSTRUCTURED MATERIALS
RADIATION EFFECTS
SILICA
STABILIZATION
VACUUM EVAPORATION
AMORPHOUS STRUCTURES
HIGH DRUG LOADINGS
LOADING CAPACITIES
MESOPOROUS SILICA
PULSED ELECTRON BEAMS
SEDIMENTATION STABILITY
STABILIZED SUSPENSION
SYNTHESIZED MATERIALS
TARGETED DRUG DELIVERY
URI: http://elar.urfu.ru/handle/10995/75478
Access: info:eu-repo/semantics/openAccess
Conference name: 6th International Congress on Energy Fluxes and Radiation Effects 2018, EFRE 2018
Conference date: 16 September 2018 through 22 September 2018
RSCI ID: 38679311
SCOPUS ID: 85058219332
WOS ID: 000546577800204
PURE ID: 8414250
ISSN: 1742-6588
DOI: 10.1088/1742-6596/1115/4/042067
Sponsorship: This work was performed within a support of the Russian Science Foundation No. 16-16-04038).
RSCF project card: 16-16-04038
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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