Temperature-related change in the properties relevant to drug delivery of poly(ethylene glycol)–poly(d,l-lactide) block copolymer micelles in aqueous milieu
Abstract
The block copolymers of poly(ethylene glycol) and poly(D,L-lactide) (PEG-PDLLA), the latter having a glass transition temperature (T(g)) around the physiological condition, was self-assembled into polymer micelles with a narrow and unimodal distribution in aqueous milieu either by dialysis or by the ultrasonication-aided dispersion method. The 1H NMR measurement of the PEG-PDLLA micelles in D(2)O revealed a gradual increase in the chain mobility of PDLLA segment in the core of the micelles at a temperature range above the T(g) of PDLLA. The critical association concentration (c.a.c.) of the PEG-PDLLA micelles was determined at various temperatures (25-55 degrees C) using pyrene as a probe to monitor the change in the polarity of the microenvironment in the micelle. An Arrhenius plot of the c.a.c. (ln(c.a.c.) versus 1/T) exhibited a break near T(g) of PDLLA. In sharp contrast with the linear decrease in ln(c.a.c.) versus 1/T in the region above the T(g), there was observed an almost constant c.a.c. (7-8 mg/l) regardless of the temperature change below the T(g). Furthermore, the chain exchange reaction between micelles was investigated based on the migration of the end-tagged block copolymers (alpha-lactosyl-PEG-PDLLA and omega-pyrenyl-PEG-PDLLA). The change in the binding affinity of the fluorescent micelles toward the RCA-1 lectin immobilized column was monitored with time to estimate the chain exchange. Consequently, appreciable acceleration in the chain exchange rate was revealed by increasing the surrounding temperature indicating the core mobility to be a substantial factor for inter-micellar chain migration. These results indicate that the engineering of the thermal characteristics of the core-forming segment of the block copolymer should be one of the crucial factors for optimizing the properties of the polymer micelles used for drug delivery.
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Nanomicelles have shown lower dissociation kinetics after dilution, around 1000-fold slower compared to conventional surfactant micelles.
“As reported, the nanomicelles have shown lower dissociation kinetics after dilution around 1000-fold slower compared to conventional surfactant micelles.”
From Recent Advances in Nanomicelles Delivery Systems. (2020) · cites this paper as [10]
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References 33 · Cited by 140
- Authors
- Yamamoto, Y., Yasugi, K., Harada, A., Nagasaki, Y., & Kataoka, K.
- Affiliations
- The University of Tokyo (JP)
- Tokyo University of Science (JP)
- Corresponding author
- Kataoka, Kazunori
- Venue
- Journal of Controlled Release
- Publisher
- Elsevier BV
- Published
- 2002-08
- Volume
- 82
- Issue
- 2-3
- Pages
- 359-371
- ISSN
- 0168-3659 (ISSN-L)
- OpenAlex
- W1973758133
- Cited by
- 140
- References
- 33
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 3 · 2023: 4 · 2022: 4 · 2021: 6 · 2020: 6 · 2019: 4 · 2018: 4 · 2017: 5 · 2016: 3 · 2015: 6 · 2014: 10 · 2013: 7 · 2012: 4
- FWCI
- 5.15
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Controlled Release (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Physical Sciences › Chemistry › Organic Chemistry › Surfactants and Colloidal Systems
- Keywords
- polymeric micelles, glass transition temperature, temperature dependence, critical association concentration, chain mobility, chain exchange, pyrene probe, drug delivery, micelle self-assembly
- MeSH terms
- Drug Carriers, Micelles, Molecular Weight, Magnetic Resonance Spectroscopy, Polyesters, Polyethylene Glycols, Temperature, Deuterium Oxide
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