Galant Céline, Kjøniksen Anna-Lena, Nguyen Giao T M, Knudsen Kenneth D, Nyström Bo
Department of Physics, Institute for Energy Technology, Post Office Box 40, N-2027 Kjeller, Norway.
J Phys Chem B. 2006 Jan 12;110(1):190-5. doi: 10.1021/jp0518759.
The formation of associative networks in semidilute aqueous solutions of hydrophobically modified alginate (HM-alginate) is dependent on intermolecular hydrophobic interactions. Addition of beta-cyclodextrin (beta-CD) monomers to the system provides decoupling of these associations via inclusion complex formation with the polymer hydrophobic tails. This results in a dramatic decrease in the viscoelastic response of the system and a more extended local structure of the polymer chains, as shown by small-angle neutron scattering (SANS) measurements. The zero-shear viscosity decreases about an order of magnitude when the beta-CD concentration is increased from 0 to 12 mm. The lifetime of the associative network decreases strongly with increasing levels of beta-CD addition. These findings clearly demonstrate that the hydrophobic association effect is efficiently reduced as the amount of beta-CD is increased. In the framework of drug delivery, this effect may be useful to improve the release of therapeutic molecules that can be entrapped in the polymer matrix.
在疏水改性藻酸盐(HM - 藻酸盐)的半稀释水溶液中,缔合网络的形成依赖于分子间的疏水相互作用。向体系中添加β - 环糊精(β - CD)单体,通过与聚合物疏水尾部形成包合物,使这些缔合作用解耦。这导致体系的粘弹性响应显著降低,聚合物链的局部结构更加伸展,如小角中子散射(SANS)测量所示。当β - CD浓度从0增加到12 mM时,零剪切粘度降低约一个数量级。缔合网络的寿命随着β - CD添加量的增加而强烈缩短。这些发现清楚地表明,随着β - CD量的增加,疏水缔合效应得到有效降低。在药物递送的框架下,这种效应可能有助于改善可包封在聚合物基质中的治疗分子的释放。