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Functionalization of Biotinylated Polyethylene Glycol on Live Magnetotactic Bacteria Carriers for Improved Stealth Properties
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Title
Functionalization of Biotinylated Polyethylene Glycol on Live Magnetotactic Bacteria Carriers for Improved Stealth Properties
DGIST Authors
Chaturvedi, RichaKang, YuminEom, YunjiTorati, Sri RamuluKim, CheolGi
Issued Date
2021-10
Citation
Chaturvedi, Richa. (2021-10). Functionalization of Biotinylated Polyethylene Glycol on Live Magnetotactic Bacteria Carriers for Improved Stealth Properties. doi: 10.3390/biology10100993
Type
Article
Author Keywords
magnetotactic bacteriabiotinpolyethylene glycolcytotoxicitydrug deliverystealth property
Keywords
DRUG-DELIVERY SYSTEMNANOPARTICLESACTUATORSLIPOSOMES
ISSN
2079-7737
Abstract
The early removal of drug delivery agents before reaching the affected target remains an area of interest to researchers. Several magnetotactic bacteria (MTB) have been used as self-propelled drug delivery agents, and they can also be controlled by an external magnetic field. By attaching the PEG–biotin polymer, the bacteria are turned into a stealth material that can escape from the phagocy-tosis process and reach the area of interest with the drug load. In the study, we developed a potential drug carrier by attaching the PEG–biotin to the MTB-through-NHS crosslinker to form a MTB/PEG– biotin complex. The attachment stability, efficacy, and bacterial viability upon attachment of the PEG– biotin polymer were investigated. Biological applications were carried out using a cytotoxicity assay of THP-1 cells, and the results indicate that the MTB/PEG–biotin complex is less harmful to cell viability compared to MTB alone. Along with cytotoxicity, an assay for cell association was also evaluated to assess the complex as a potential stealth material. The development of these complexes focuses on an easy, time-saving, and stable technique of polymer attachment with the bacteria, without damaging the cell’s surface, so as to make it a strong and reliable delivery agent. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
URI
http://hdl.handle.net/20.500.11750/15753
DOI
10.3390/biology10100993
Publisher
MDPI AG
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