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Activated Carbon-Enriched Electrospun-Produced Scaffolds for Drug Delivery/Release in Biological Systems Full article

Journal International Journal of Molecular Sciences
ISSN: 1422-0067 , E-ISSN: 1661-6596
Output data Year: 2023, Volume: 24, Number: 7, Article number : 6713, Pages count : 15 DOI: 10.3390/ijms24076713
Tags activated carbon; controlled release; drug delivery; electrospinning; sirolimus
Authors Nazarkina Zhanna K. 1 , Stepanova Alena O. 1,2 , Chelobanov Boris P. 1,3 , Kvon Ren I. 4 , Simonov Pavel A. 3 , Karpenko Andrey A. 2 , Laktionov Pavel P. 1,2
Affiliations
1 Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences, 630090 Novosibirsk, Russia
2 Meshalkin National Medical Research Center, Ministry of Health of the Russian Federation, 630055 Novosibirsk, Russia
3 Department of Natural Sciences, Novosibirsk State University, 630090 Novosibirsk, Russia
4 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, 630090 Novosibirsk, Russia

Funding (2)

1 Ministry of Science and Higher Education of the Russian Federation 075-00404-21-00 (121031300042-1)
2 Ministry of Health of the Russian Federation 056-00125-21-00 AVRB-2021-0001 (121032300337-5)

Abstract: To vectorize drug delivery from electrospun-produced scaffolds, we introduce a thin outer drug retention layer produced by electrospinning from activated carbon nanoparticles (ACNs)-enriched polycaprolacton (PCL) suspension. Homogeneous or coaxial fibers filled with ACNs were produced by electrospinning from different PCL-based suspensions. Stable ACN suspensions were selected by sorting through solvents, stabilizers and auxiliary components. The ACN-enriched scaffolds produced were characterized for fiber diameter, porosity, pore size and mechanical properties. The scaffold structure was analyzed by scanning electron microscopy and X-ray photoelectron spectroscopy. It was found that ACNs were mainly coated with a polymer layer for both homogeneous and coaxial fibers. Drug binding and release from the scaffolds were tested using tritium-labeled sirolimus. We showed that the kinetics of sirolimus binding/release by ACN-enriched scaffolds was determined by the fiber composition and differed from that obtained with a free ACN. ACN-enriched scaffolds with coaxial and homogeneous fibers had a biocompatibility close to scaffold-free AC, as was shown by the cultivation of human gingival fibroblasts and umbilical vein cells on scaffolds. The data obtained demonstrated that ACN-enriched scaffolds had good physico-chemical properties and biocompatibility and, thus, could be used as a retaining layer for vectored drug delivery.
Cite: Nazarkina Z.K. , Stepanova A.O. , Chelobanov B.P. , Kvon R.I. , Simonov P.A. , Karpenko A.A. , Laktionov P.P.
Activated Carbon-Enriched Electrospun-Produced Scaffolds for Drug Delivery/Release in Biological Systems
International Journal of Molecular Sciences. 2023. V.24. N7. 6713 :1-15. DOI: 10.3390/ijms24076713 WOS Scopus РИНЦ AN PMID OpenAlex
Dates:
Submitted: Mar 10, 2023
Accepted: Apr 1, 2023
Published print: Apr 1, 2023
Published online: Apr 4, 2023
Identifiers:
Web of science: WOS:000970207300001
Scopus: 2-s2.0-85152323651
Elibrary: 53235879
Chemical Abstracts: 2023:810305
PMID: 37047685
OpenAlex: W4362559320
Citing:
DB Citing
Scopus 6
Web of science 4
Elibrary 4
OpenAlex 7
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