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Aggregation and Thermoresponsive Properties of New Star Block Copolymers with a Cholic Acid Core

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Journal Langmuir
Specialty Chemistry
Date 2011 Aug 2
PMID 21800871
Citations 4
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Abstract

Poly(allyl glycidyl ether) (PAGE) and poly(ethylene glycol) (PEG) blocks were sequentially grown via anionic polymerization to form four block copolymer arms on a cholic acid (CA) core, yielding star block copolymers (CA(AGE(8)-b-EG(n))(4)) with low polydispersities (ca. 1.05). The introduction of PAGE segments into CA(PEG)(4) significantly reduced their crystallinity. The polymers can aggregate in water at room temperature above their critical aggregation concentration. The copolymers are thermoresponsive; their behavior in aqueous solutions was studied by the use of UV-visible spectroscopy, dynamic light scattering, and transmission electron microscopy. Their cloud points vary from 13 to 55 °C with increasing length of the PEG segments. Double thermoresponsive behavior was observed with short PEG segments because of a two-step transition process: small micelles are formed upon heating and then further aggregate into micellar clusters through the association of PEG chains.

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References
1.
Leckband D, Sheth S, Halperin A . Grafted poly(ethylene oxide) brushes as nonfouling surface coatings. J Biomater Sci Polym Ed. 1999; 10(10):1125-47. DOI: 10.1163/156856299x00720. View

2.
Qin G, Cai C . Oxidative degradation of oligo(ethylene glycol)-terminated monolayers. Chem Commun (Camb). 2010; (34):5112-4. DOI: 10.1039/b911155g. View

3.
Yam C, Lopez-Romero J, Gu J, Cai C . Protein-resistant monolayers prepared by hydrosilylation of alpha-oligo(ethylene glycol)-omega-alkenes on hydrogen-terminated silicon (111) surfaces. Chem Commun (Camb). 2004; (21):2510-1. DOI: 10.1039/b401499e. View

4.
Holland N, Qiu Y, Ruegsegger M, Marchant R . Biomimetic engineering of non-adhesive glycocalyx-like surfaces using oligosaccharide surfactant polymers. Nature. 1998; 392(6678):799-801. DOI: 10.1038/33894. View

5.
Lasseter Clare T, Clare B, Nichols B, Abbott N, Hamers R . Functional monolayers for improved resistance to protein adsorption: oligo(ethylene glycol)-modified silicon and diamond surfaces. Langmuir. 2005; 21(14):6344-55. DOI: 10.1021/la050362q. View