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

被引:2
|
作者
Majercikova, Monika [1 ]
Nadazdy, Peter [2 ]
Chorvat, Dusan [3 ]
Satrapinskyy, Leonid [4 ]
Valentova, Helena [5 ]
Kronekova, Zuzana [1 ]
Siffalovic, Peter [2 ,6 ]
Kronek, Juraj [1 ]
Zahoranova, Anna [7 ]
机构
[1] Slovak Acad Sci, Polymer Inst, Dept Biomat Res, Dubravska Cesta 9, Bratislava 84541, Slovakia
[2] Slovak Acad Sci, Inst Phys, Dubravska Cesta 9, Bratislava 84511, Slovakia
[3] Int Laser Ctr, Dept Biophoton, Ilkovicova 3, Bratislava 84104, Slovakia
[4] Comenius Univ, Fac Math Phys & Informat, Dept Expt Phys, Bratislava 84248, Slovakia
[5] Charles Univ Prague, Fac Math & Phys, Ke Karlovu 3, Prague 12116 2, Czech Republic
[6] Slovak Acad Sci, Ctr Adv Mat Applicat, Dubravska Cesta 9, Bratislava 84511, Slovakia
[7] Vienna Univ Technol, Inst Appl Synthet Chem, Getreidemarkt 9-163MC, A-1060 Vienna, Austria
基金
欧盟地平线“2020”; 奥地利科学基金会;
关键词
ring-opening polymerization; self-assembly; stimuli-responsive polymers; drug delivery systems; crystallization; DRUG-DELIVERY; BLOCK-COPOLYMERS; NANOCARRIERS; CYTOTOXICITY; TEMPERATURE; SYSTEMS; POLY(2-ETHYL-2-OXAZOLINE); MICELLES; POLYMERS; LCST;
D O I
10.3390/polym13091357
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
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.
引用
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页数:18
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