Skin protein-derived peptide-conjugated vesicular nanocargos for selected skin cell targeting and consequent activation
- Authors
- Cho, Jung Hyeon; Kang, Jeong Yi; Kim, Seulgi; Baek, Hwi Ra; Kim, Junoh; Jang, Kwang-Suk; Kim, Jin Woong
- Issue Date
- Jun-2021
- Publisher
- Royal Society of Chemistry
- Citation
- Journal of Materials Chemistry B, v.9, no.24, pp 4956 - 4962
- Pages
- 7
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Materials Chemistry B
- Volume
- 9
- Number
- 24
- Start Page
- 4956
- End Page
- 4962
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/118793
- DOI
- 10.1039/d1tb00935d
- ISSN
- 2050-750X
2050-7518
- Abstract
- Several studies have reported that a drug nanocarrier conjugated with ligands having cell binding ability improves drug delivery performance, but multiple cell-targeting and the resultant activation in designated cells has not been investigated yet. This study reports a skin cell multi-targeting vesicular nanocargo system. We selectively conjugated several skin protein-derived cell-targeting peptides (CTPs), including KTTKS, NAP-amide, and Lam332, to amphiphilic polymer-reinforced lipid nanovesicles (PLNVs) to specifically target fibroblasts, melanocytes, and keratinocytes, respectively, through effective association with the corresponding cell membrane receptors. We then showed that CTP-conjugated PLNVs specifically bind to the designated skin cells, even in a mixture of different types of skin cells, eventually leading to skin cell multi-targeting and consequent activation. These results highlight that this CTP-conjugated PLNV system has significant potential for developing an intelligent cellular drug delivery technology for dermatological applications. © The Royal Society of Chemistry 2021.
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