4.7 Article

Effect of Dexamethasone on Thermoresponsive Behavior of Poly(2-Oxazoline) Diblock Copolymers

Journal

POLYMERS
Volume 13, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/polym13091357

Keywords

ring-opening polymerization; self-assembly; stimuli-responsive polymers; drug delivery systems; crystallization

Funding

  1. Austrian Science Fund (FWF) [M 2805-N]
  2. Slovak Grant Agency VEGA [1/0602/19, 2/0172/21]
  3. Horizon 2020 project LASERLAB-EUROPE [871124]
  4. Research & Innovation Operational Programme - ERDF [313021T081]

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This study investigated the influence of dexamethasone on the thermoresponsive behavior of diblock copolymers, revealing that the addition of dexamethasone lowered the cloud point temperature of one copolymer and resulted in the formation of microparticles. The characteristics of the microparticles were influenced by the structure and concentration of the copolymer, the drug concentration, and the temperature.
Thermoresponsive polymers play an important role in designing drug delivery systems for biomedical applications. In this contribution, the effect of encapsulated hydrophobic drug dexamethasone on thermoresponsive behavior of diblock copolymers was studied. A small series of diblock copoly(2-oxazoline)s was prepared by combining thermoresponsive 2-n-propyl-2-oxazoline (nPrOx) and hydrophilic 2-methyl-2-oxazoline (MeOx) in two ratios and two polymer chain lengths. The addition of dexamethasone affected the thermoresponsive behavior of one of the copolymers, nPrOx(20)-MeOx(180), in the aqueous medium by shifting the cloud point temperature to lower values. In addition, the formation of microparticles containing dexamethasone was observed during the heating of the samples. The morphology and number of microparticles were affected by the structure and concentration of copolymer, the drug concentration, and the temperature. The crystalline nature of formed microparticles was confirmed by polarized light microscopy, confocal Raman microscopy, and wide-angle X-ray scattering. The results demonstrate the importance of studying drug/polymer interactions for the future development of thermoresponsive drug carriers.

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