Biomimetic pH/redox dual stimuli‐responsive zwitterionic polymer block poly(L‐histidine) micelles for intracellular delivery of doxorubicin into tumor cells. Issue 12 (13th April 2017)
- Record Type:
- Journal Article
- Title:
- Biomimetic pH/redox dual stimuli‐responsive zwitterionic polymer block poly(L‐histidine) micelles for intracellular delivery of doxorubicin into tumor cells. Issue 12 (13th April 2017)
- Main Title:
- Biomimetic pH/redox dual stimuli‐responsive zwitterionic polymer block poly(L‐histidine) micelles for intracellular delivery of doxorubicin into tumor cells
- Authors:
- John, Johnson V.
Uthaman, Saji
Augustine, Rimesh
Manickavasagam Lekshmi, Kamali
Park, In‐Kyu
Kim, Il - Abstract:
- ABSTRACT: A series of pH/redox dual stimuli‐responsive poly(2‐methacryloyloxyethyl phosphorylcholine)25 ‐ block ‐poly(l ‐histidine) n (p[MPC])25 ‐ b ‐p[His]n, n = 20, 35, 50, and 75) copolymers consisting of a pH‐responsive p(His) n block and a biocompatible phospholipid analog p(MPC) block connected by a redox‐responsive disulfide linker have been synthesized. The block copolymers are self‐assembled into uniform micelles (∼100 nm) in which doxorubicin (Dox) is efficiently encapsulated. The in vitro release profile shows an enhanced release of Dox at low pH (5.0) in 10 mM glutathione (GSH). The in vitro cell viability assays performed using various cell lines show that the blank hybrid micelles have no acute or intrinsic toxicity. A pH‐dependent cytotoxicity is observed with the Dox‐loaded micelles, especially at pH 5.0. Moreover, confocal microscopy images and flow cytometry results show the pH‐dependent cellular uptake of Dox‐loaded micelles. Therefore, the Dox‐loaded micelles can be considered a good candidate for cancer therapy. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem.2017, 55, 2061–2070 Abstract : A series of synthetic polymer/polypeptide block copolymers consisting of a pH‐responsive polypeptide unit and a biocompatible and soluble zwitterionic polymer unit are designed. Both units are connected by a redox‐responsive disulfide linkers. The new block copolymers self‐assemble to form uniform micelles around 100 nm in size, and they showABSTRACT: A series of pH/redox dual stimuli‐responsive poly(2‐methacryloyloxyethyl phosphorylcholine)25 ‐ block ‐poly(l ‐histidine) n (p[MPC])25 ‐ b ‐p[His]n, n = 20, 35, 50, and 75) copolymers consisting of a pH‐responsive p(His) n block and a biocompatible phospholipid analog p(MPC) block connected by a redox‐responsive disulfide linker have been synthesized. The block copolymers are self‐assembled into uniform micelles (∼100 nm) in which doxorubicin (Dox) is efficiently encapsulated. The in vitro release profile shows an enhanced release of Dox at low pH (5.0) in 10 mM glutathione (GSH). The in vitro cell viability assays performed using various cell lines show that the blank hybrid micelles have no acute or intrinsic toxicity. A pH‐dependent cytotoxicity is observed with the Dox‐loaded micelles, especially at pH 5.0. Moreover, confocal microscopy images and flow cytometry results show the pH‐dependent cellular uptake of Dox‐loaded micelles. Therefore, the Dox‐loaded micelles can be considered a good candidate for cancer therapy. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem.2017, 55, 2061–2070 Abstract : A series of synthetic polymer/polypeptide block copolymers consisting of a pH‐responsive polypeptide unit and a biocompatible and soluble zwitterionic polymer unit are designed. Both units are connected by a redox‐responsive disulfide linkers. The new block copolymers self‐assemble to form uniform micelles around 100 nm in size, and they show efficient pH/redox dual‐stimuli responsive drug delivery into tumor cells. … (more)
- Is Part Of:
- Journal of polymer science. Volume 55:Issue 12(2017)
- Journal:
- Journal of polymer science
- Issue:
- Volume 55:Issue 12(2017)
- Issue Display:
- Volume 55, Issue 12 (2017)
- Year:
- 2017
- Volume:
- 55
- Issue:
- 12
- Issue Sort Value:
- 2017-0055-0012-0000
- Page Start:
- 2061
- Page End:
- 2070
- Publication Date:
- 2017-04-13
- Subjects:
- biopolymers -- block copolymers -- drug delivery -- peptides -- responsive polymers
547 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0518 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pola.28602 ↗
- Languages:
- English
- ISSNs:
- 0887-624X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5041.002050
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2121.xml