Synthesis of sub-50 nm bio-inspired silica particles using a C-terminal-modified ferritin template with a silica-forming peptide
- Authors
- Nguyen, Thi Khoa My; Ki, Mi Ran; Son, Ryeo Gang; Kim, Kyung Hee; Hong, Junghwa; Pack, Seung Pil
- Issue Date
- 25-9월-2021
- Publisher
- ELSEVIER SCIENCE INC
- Keywords
- Biosilica nanoparticles; Drug delivery; Ferritin; Silica-forming peptide; Silicification
- Citation
- JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY, v.101, pp.262 - 269
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
- Volume
- 101
- Start Page
- 262
- End Page
- 269
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/136305
- DOI
- 10.1016/j.jiec.2021.06.005
- ISSN
- 1226-086X
- Abstract
- Silica-forming peptides (SFPs) and the SFP-modified structural proteins can be used as templates for the synthesis of biosilica nanoparticles (NPs). However, such biomolecule-mediated synthesis showed limitations for the generation of NPs with sizes sub-50 nm. In this study, the SFP sequences (KPSHHHHHTGAN and KPTHHHHHHDG for Kps and Kpt, respectively) were fused to the C-terminus of the human ferritin heavy chain (Fn), resulting in the SFP moieties in the inner space of Fn (termed FncKps and Fn-cKpt). Using Fn-cSFP templates for silicification in two-phase system, the Fn-cKps@SiO2 and Fn-cKpt@SiO2 NPs were generated in mean diameters of 26 and 28 nm, respectively. Also, we employed biosilica NPs sub-50 nm for a doxorubicin (Dox) delivery system (application model). Fn-cKpt@SiO2 NPs exhibited a high loading efficiency compared to Fn-cKpt only (1.7-fold) and prolonged release patterns with Dox. Most importantly, the uptake of Fn-cKpt@SiO2 into cancer cells was increased so that the efficient delivery of Dox to the cell inside was observed. The uniform generation of biosilica NPs sub-50 nm obtained here is a new achievement. Together with the ideal pH-dependent drug release, the size-controlled design of biosilica will be a useful strategy for efficient delivery of chemical drugs to target cells. (C) 2021 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
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Collections - Graduate School > Department of Control and Instrumentation Engineering > 1. Journal Articles
- Graduate School > Department of Biotechnology and Bioinformatics > 1. Journal Articles
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