The DOI matches its Crossref record.
Thermogelling Poly(caprolactone-b-ethylene glycol-b-caprolactone) Aqueous Solutions
Abstract
Poly(caprolactone- b -ethylene glycol- b -caprolactone) (PCL−PEG−PCL) triblock copolymer aqueous solution (>15 wt %) undergoes the sol−gel−sol transition as the temperature increases from 10 to 60 °C. The mechanism and structure−property relationship of the sol−gel transition were investigated. In particular, compared with the PEG−PCL−PEG triblock copolymers recently reported by our group, PCL−PEG−PCL has (1) a synthetic advantage without a hexamethylene diisocyanate coupling step, (2) a wider gel window of over 15−32 wt %, and (3) a larger gel modulus. Both PEG−PCL−PEG and PCL−PEG−PCL polymers are an important progress in the biodegradable thermogelling system in that they can be lyophilized in a powder form, are easy to handle, are easy to redissolve to a clear solution, and show little syneresis through the gel phase.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cited by
Responsive polymers in controlled drug delivery
Bajpai, A. K., Shukla, S. K., Bhanu, S., & Kankane, S. (2008) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2008.07.005 · Cited by 1,391
Hydrogels in a historical perspective: From simple networks to smart materials
Buwalda, S. J., Boere, K. W. M., Dijkstra, P. J., Feijen, J., Vermonden, T., & Hennink, W. E. (2014) · Journal of Controlled Release · doi:10.1016/j.jconrel.2014.03.052 · Cited by 994
Hydrogel scaffolds for tissue engineering: the importance of polymer choice
Spicer, C. D. (2020) · Polymer Chemistry · doi:10.1039/c9py01021a · Cited by 527
Injectable Biodegradable Hydrogels
Nguyen, M. K., & Lee, D. S. (2010) · Macromolecular Bioscience · doi:10.1002/mabi.200900402 · Cited by 481
PEG-based thermosensitive and biodegradable hydrogels
Shi, J., Yu, L., & Ding, J. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2021.04.009 · Cited by 341
Fabrication of Bioinspired Hydrogels: Challenges and Opportunities
Fan, H., & Gong, J. P. (2020) · Macromolecules · doi:10.1021/acs.macromol.0c00238 · Cited by 292
Responsive reversible hydrogels from associative “smart” macromolecules
Tsitsilianis, C. (2010) · Soft Matter · doi:10.1039/b923947b · Cited by 278
Advances in biodegradable and injectable hydrogels for biomedical applications
Li, Y., Yang, H. Y., & Lee, D. S. (2021) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.12.008 · Cited by 261
Castillo, R. V., & Müller, A. J. (2009) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2009.03.002 · Cited by 253
Chatterjee, S., Hui, P. C.-L., & Kan, C.-W. (2018) · Polymers · doi:10.3390/polym10050480 · Cited by 196
Gong, C., Qian, Z., Liu, C., Huang, M., Gu, Y., Wen, Y., Kan, B., Wang, K., Dai, M., Li, X., et al. (2007) · Smart Materials and Structures · doi:10.1088/0964-1726/16/3/043 · Cited by 73
Smart hydrogel-functionalized textile system with moisture management property for skin application
Wang, X., Hu, H., Yang, Z., He, L., Kong, Y., Fei, B., & Xin, J. H. (2014) · Smart Materials and Structures · doi:10.1088/0964-1726/23/12/125027 · Cited by 58
Liu, M., Chen, W., Zhang, X., Su, P., Yue, F., Zeng, S., & Du, S. (2020) · European Journal of Pharmaceutical Sciences · doi:10.1016/j.ejps.2020.105373 · Cited by 50
Sun, L., Shen, L., Zhu, M., Dong, C., & Wei, Y. (2010) · Journal of Polymer Science Part A: Polymer Chemistry · doi:10.1002/pola.24255 · Cited by 40
Palacios, J. K., Mugica, A., Zubitur, M., & Müller, A. J. (2018) · Crystallization in Multiphase Polymer Systems · doi:10.1016/b978-0-12-809453-2.00006-2 · Cited by 18
Buwalda, S. J., Dijkstra, P. J., & Feijen, J. (2012) · Macromolecular Chemistry and Physics · doi:10.1002/macp.201100640 · Cited by 17
Metadata
- Authors
- Bae, S. J., Suh, J. M., Sohn, Y. S., Bae, Y. H., Kim, S. W., & Jeong, B.
- Venue
- Macromolecules
- Publisher
- American Chemical Society (ACS)
- Published
- 2005-05-17
- Volume
- 38
- Issue
- 12
- Pages
- 5260-5265
- ISSN
- 0024-9297 (ISSN-L)
- 1520-5835
- OpenAlex
- W1980543487
- Cited by
- 285
- References
- 0
- FWCI
- 7.01
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.