Effect of Polymer Composition on Rheological and Degradation Properties of Temperature-Responsive Gelling Systems Composed of Acyl-Capped PCLA-PEG-PCLA

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• 作者：Audrey Petit ; Benno M眉ller ; Ronald Meijboom ; Peter Bruin ; Frank van de Manakker ; Marjan Versluijs-Helder ; Leo G. J. de Leede ; Albert Doornbos ; Mariana Landin ; Wim E. Hennink ; Tina Vermonden
• 刊名：Biomacromolecules
• 出版年：2013
• 出版时间：September 9, 2013
• 年：2013
• 卷：14
• 期：9
• 页码：3172-3182
• 全文大小：592K
• 年卷期：v.14,no.9(September 9, 2013)
• ISSN：1526-4602

文摘

In this study, the ability to modulate the rheological and degradation properties of temperature-responsive gelling systems composed of acyl-capped poly(蔚-caprolactone-co-lactide)-b-poly(ethylene glycol)-b-poly(蔚-caprolactone-co-lactide) (PCLA-PEG-PCLA) triblock copolymers was investigated. Eight polymers with varying molecular weight of PCLA, caproyl/lactoyl ratio (CL/LA) and capped with either acetyl- or propionyl-groups were synthesized by ring-opening polymerization of l-lactide and 蔚-caprolactone in toluene using PEG as initiator and tin(II) 2-ethylhexanoate as catalyst, and subsequently reacted in solution with an excess of acyl chloride to yield fully acyl-capped PCLA-PEG-PCLA. The microstructure of the polymers was determined by ¹H NMR, and the thermal properties and crystallinity of the polymers in dry state and in 25 wt % aqueous systems were studied by differential scanning calorimetry and X-ray diffraction. Rheological and degradation/dissolution properties of aqueous systems composed of the polymers in 25 wt % aqueous systems were studied. ¹H NMR analysis revealed that the monomer sequence in the PCLA blocks was not fully random, resulting in relatively long CL sequences, even though transesterification was demonstrated by the enrichment with lactoyl units and the presence of PEG鈥揙H end groups. Except the most hydrophilic polymer composed of acetyl-capped PCLA₁₄₀₀-PEG₁₅₀₀-PCLA₁₄₀₀ having a CL/LA molar ratio of 2.5, the polymers at 25 wt % in buffer were sols below room temperature and transformed into gels between room temperature and 37 掳C, which makes them suitable as temperature-responsive gelling systems for drug delivery. Over a period of weeks at 37 掳C, the systems containing polymers with long CL sequences (8 CL) and propionyl end-groups became semicrystalline as shown by X-ray diffraction analysis. Degradation of the gels by dissolution at 37 掳C took 100鈥?50 days for the amorphous gels and 250鈥?00 days for the semicrystalline gels. In conclusion, this study shows that changes in the polymer composition allow an easy but significant modulation of rheological and degradation properties.