Novel Self-assembled Hydrogels by Stereocomplex Formation in Aqueous Solution of Enantiomeric Lactic Acid Oligomers Grafted To Dextran

• Published in: Macromolecules Vol. 33; no. 10; pp. 3680 - 3686
• Main Authors: de Jong, S. J, De Smedt, S. C, Wahls, M. W. C, Demeester, J, Kettenes-van den Bosch, J. J, Hennink, W. E
• Format: Journal Article
• Language: English
• Published: American Chemical Society 16.05.2000
• ISSN: 0024-9297; 1520-5835
• DOI: 10.1021/ma992067g

This paper describes a novel hydrogel concept, which is based on self-assembling of enantiomeric lactic acid oligomers (stereocomplex formation) grafted to dextran. The hydrogels are prepared in an all-aqueous environment. For this purpose, l- and d-lactic acid oligomers were coupled to dextran, yielding dex−(l)lactate and dex−(d)lactate, respectively. Upon dissolving each product in water separately and mixing the solutions, we observed that a hydrogel is formed at room temperature as demonstrated by rheological measurements. The storage modulus of the obtained hydrogel strongly decreased upon heating to 80 °C, while it was restored upon cooling to 20 °C, demonstrating the thermoreversibility and the physical nature of the cross-links. Rheological experiments with monodisperse lactic acid oligomers grafted to dextran showed that the degree of polymerization (DP) of the lactic acid oligomers must be at least 11 to obtain a hydrogel. The hydrogel characteristics can be modulated by varying the degree of polymerization (DP, number of lactate units per oligomer) and the degree of substitution (DS, number of lactic acid side chains per 100 glucopyranose units) of the dex−lactate products, as well as the water content of the dex−lactate solutions. Stronger gels were obtained by increasing the DP and DS and by decreasing the water content. FTIR−photoacoustic (PA) analysis demonstrated that in the hydrogels stereocomplexes were formed between the lactic acid oligomers of opposite chirality.