Tailorable degradation of pH-responsive all polyether micelles: Via copolymerisation with varying acetal groups

Jaeeun Song, Eunbyul Hwang, Yungyeong Lee, L. Palanikumar, Soo Hyung Choi, Ja Hyoung Ryu, Byeong-Su Kim

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Smart drug delivery in a site-specific and time-controlled manner is critical for reducing the side effects of the drug while maximizing the therapeutic efficacy. Herein, we describe an efficient approach to control the degradation kinetics of polyether micelles under acidic conditions using random copolymers of functional epoxide monomers bearing different acetal groups. The amphiphilic block copolymers, poly(ethylene glycol)-block-poly(ethoxyethyl glycidyl ether-co-tetrahydropyranyl glycidyl ether)s (PEG-b-P(EEGE-co-TGE))s, are synthesized by the anionic ring-opening polymerisation of the pH-responsive novel epoxide monomers ethoxyethyl glycidyl ether (EEGE) and tetrahydropyranyl glycidyl ether (TGE) in varying ratios. The random block copolymers are carefully characterized by 1 H NMR, GPC, and DSC and the copolymerisation kinetics are evaluated using in situ 1 H NMR analysis. The critical micelle concentrations, loading efficiencies, and size distributions of the copolymer micelles show a saturation point over a critical TGE ratio. Interestingly, the degradation and subsequent release kinetics of the micelles under acidic conditions are remarkably different when the composition of the acetal groups is varied. The superior biocompatibility coupled with the highly tailorable release kinetics is anticipated to lead to a versatile platform for smart drug delivery systems.

Original languageEnglish
Pages (from-to)582-592
Number of pages11
JournalPolymer Chemistry
Volume10
Issue number5
DOIs
Publication statusPublished - 2019 Feb 7

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Acetals
Polyethers
Micelles
Copolymerization
Ethers
Degradation
Kinetics
Epoxy Compounds
Polyethylene glycols
Block copolymers
Bearings (structural)
Copolymers
Monomers
Nuclear magnetic resonance
Anionic polymerization
Ethylene Glycol
Critical micelle concentration
Ring opening polymerization
Drug Delivery Systems
Drug-Related Side Effects and Adverse Reactions

All Science Journal Classification (ASJC) codes

  • Bioengineering
  • Biochemistry
  • Polymers and Plastics
  • Organic Chemistry

Cite this

Song, Jaeeun ; Hwang, Eunbyul ; Lee, Yungyeong ; Palanikumar, L. ; Choi, Soo Hyung ; Ryu, Ja Hyoung ; Kim, Byeong-Su. / Tailorable degradation of pH-responsive all polyether micelles : Via copolymerisation with varying acetal groups. In: Polymer Chemistry. 2019 ; Vol. 10, No. 5. pp. 582-592.
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Tailorable degradation of pH-responsive all polyether micelles : Via copolymerisation with varying acetal groups. / Song, Jaeeun; Hwang, Eunbyul; Lee, Yungyeong; Palanikumar, L.; Choi, Soo Hyung; Ryu, Ja Hyoung; Kim, Byeong-Su.

In: Polymer Chemistry, Vol. 10, No. 5, 07.02.2019, p. 582-592.

Research output: Contribution to journalArticle

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