期刊
BIOMACROMOLECULES
卷 23, 期 12, 页码 5361-5372出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.biomac.2c01226
关键词
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资金
- Royal Golden Jubilee (RGJ) Ph.D. Program through the National Research Council of Thailand (NRCT) [PHD/0186/2559]
- National Nanotechnology Center (NANOTEC)
- National Science and Technology Development Agency (NSTDA), Thailand - National Research Council of Thailand (NRCT)
- Thailand Science Research and Innovation Fund Chulalongkorn University [BCG66630029]
- National Research Council of Thailand (NRCT) [N42A640322]
Multistimuli-responsive polymers are important for controlled release, but their decoration is limited due to their derivation from vinyl-based monomers. In this study, polymers with different critical solution temperatures were introduced onto chitosan and hyaluronic acid, resulting in a polymer system with a multiresponsive window. By adjusting the mole ratio and pH, the encapsulation and release of lysozyme were controlled repeatably.
Multistimuli-responsive polymers are important for controlled release. Owing to the fact that these polymers are derived from vinyl-based monomers, their decoration with other molecules is limited. Polysaccharides, especially chitosan (CS) and hyaluronic acid (HA), are pH-responsive biopolymers, whose chemical structures contain reactive functional groups for feasible chemical modifications to obtain add-on functions. The present work demonstrates the introduction of polymers with upper critical solution temperature (UCST) and lower critical solution temper-ature (LCST) performances onto CS and HA, respectively. By simply varying the mole ratio between the CS-containing UCST polymer and the HA-containing LCST polymer along with adjusting the pH, a polymer system with a UCST-LCST-pH multiresponsive window can be obtained. This multiresponsive window enables us to control the encapsulation and release with repeatability as evidenced from a model study on lysozyme. The present work, for the first time, shows a simple approach to obtain multiresponsive biodegradable polymers through the formation of a single polymer complex to tailor a specific multiresponsive window.
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