Facile fabrication of highly soluble, extremely small-sized drug carriers using globular poly(ethylene glycol)
- Authors
- Lee M.[Lee M.]; Lee D.J.[Lee D.J.]; Youn Y.S.[Youn Y.S.]; Lee E.S.[Lee E.S.]
- Issue Date
- Mar-2016
- Publisher
- SAGE PUBLICATIONS LTD
- Citation
- JOURNAL OF BIOACTIVE AND COMPATIBLE POLYMERS, v.31, no.2, pp.167 - 178
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF BIOACTIVE AND COMPATIBLE POLYMERS
- Volume
- 31
- Number
- 2
- Start Page
- 167
- End Page
- 178
- URI
- https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/37468
- DOI
- 10.1177/0883911515603737
- ISSN
- 0883-9115
- Abstract
- We report extremely small-sized drug-carrying globular poly(ethylene glycol) particles. These particles were prepared using fullerene (C-60) as a backbone structure and poly(ethylene glycol) as a hydrophilic shell. All - carbon bonds in C-60 were combined with poly(ethylene glycol), which form a globular nano-cage with a hollow core (originating from the soccer-ball-shaped truncated icosahedron of C-60) and the poly(ethylene glycol) shell. Subsequently, we constructed chlorin e6-conjugated globular poly(ethylene glycol). The obtained globular poly(ethylene glycol)-chlorin e6 (average 3.6nm in diameter) was soluble in aqueous solution and enabled improved singlet oxygen generation. The preferential cellular uptake of globular poly(ethylene glycol)-chlorin e6 resulted in significant enhancement of in vitro or in vivo photodynamic tumor cell ablation under light illumination. Our approach offers a versatile strategy to create extremely small-sized drug carriers using a biocompatible polymer for various biomedical applications.
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Collections - Pharmacy > Department of Pharmacy > 1. Journal Articles
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