PCL–PEG graft copolymers with tunable amphiphilicity as efficient drug delivery systems. Issue 37 (8th September 2016)
- Record Type:
- Journal Article
- Title:
- PCL–PEG graft copolymers with tunable amphiphilicity as efficient drug delivery systems. Issue 37 (8th September 2016)
- Main Title:
- PCL–PEG graft copolymers with tunable amphiphilicity as efficient drug delivery systems
- Authors:
- Al Samad, A.
Bethry, A.
Koziolová, E.
Netopilík, M.
Etrych, T.
Bakkour, Y.
Coudane, J.
El Omar, F.
Nottelet, B. - Abstract:
- Abstract : Efficient drug delivery systems are prepared, thanks to the fine-tuning of the amphiphilicity and architecture of PCL–PEG graft copolymers via a simple photochemical approach. Abstract : The development of flexible drug delivery systems that can be tuned as a function of the drug to be delivered and of the target disease is crucial in modern medicine. For this aim, novel amphiphilic poly(ε-caprolactone)- g -poly(ethylene glycol) (PCL- g -PEG) copolymers with well-controlled design were synthesized by thiol–yne photochemistry. The grafting density and the copolymer amphiphilicity were easily controlled via the reaction parameters: concentration, reaction time, PEG length and the molar ratio between PCL and PEG or the photoinitiator in the reaction mixture. The self-assembling behavior of the copolymers was studied and a correlation between the composition of PCL- g -PEG and the nanoaggregate diameter sizes (28 to 73 nm) and critical aggregation concentrations (1.1 to 4.3 mg L −1 ) was found. The influence of copolymer amphiphilicity on the drug loading was evaluated with various drugs including anticancer drugs (paclitaxel, ABT-199), drugs to overcome multidrug resistance in cancer cells (curcumin, elacridar), an anti-inflammatory drug (dexamethasone) and an antibacterial drug (clofazimine). Finally, the influence of amphiphilicity on curcumin release and toxicity towards MCF-7 cancer cell lines was studied. The impact of the grafting density, PEG length and theAbstract : Efficient drug delivery systems are prepared, thanks to the fine-tuning of the amphiphilicity and architecture of PCL–PEG graft copolymers via a simple photochemical approach. Abstract : The development of flexible drug delivery systems that can be tuned as a function of the drug to be delivered and of the target disease is crucial in modern medicine. For this aim, novel amphiphilic poly(ε-caprolactone)- g -poly(ethylene glycol) (PCL- g -PEG) copolymers with well-controlled design were synthesized by thiol–yne photochemistry. The grafting density and the copolymer amphiphilicity were easily controlled via the reaction parameters: concentration, reaction time, PEG length and the molar ratio between PCL and PEG or the photoinitiator in the reaction mixture. The self-assembling behavior of the copolymers was studied and a correlation between the composition of PCL- g -PEG and the nanoaggregate diameter sizes (28 to 73 nm) and critical aggregation concentrations (1.1 to 4.3 mg L −1 ) was found. The influence of copolymer amphiphilicity on the drug loading was evaluated with various drugs including anticancer drugs (paclitaxel, ABT-199), drugs to overcome multidrug resistance in cancer cells (curcumin, elacridar), an anti-inflammatory drug (dexamethasone) and an antibacterial drug (clofazimine). Finally, the influence of amphiphilicity on curcumin release and toxicity towards MCF-7 cancer cell lines was studied. The impact of the grafting density, PEG length and the overall EG/CL ratio is discussed in detail. Curcumin loaded PCL- g -PEG with lower EG/CL ratios and shorter PEG chains showed higher toxicity compared to their more hydrophilic counterparts. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 4:Issue 37(2016)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 4:Issue 37(2016)
- Issue Display:
- Volume 4, Issue 37 (2016)
- Year:
- 2016
- Volume:
- 4
- Issue:
- 37
- Issue Sort Value:
- 2016-0004-0037-0000
- Page Start:
- 6228
- Page End:
- 6239
- Publication Date:
- 2016-09-08
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Biomedical materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tb# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6tb01841f ↗
- Languages:
- English
- ISSNs:
- 2050-750X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205200
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1353.xml