Coussot G, Ladner Y, Bayart C, Faye C, Vigier V, Perrin C
Institut des Biomolécules Max Mousseron-IBMM, Centre National de la Recherche Scientifique, Université de Montpellier 1, Université de Montpellier 2, Unité Mixte de Recherche 5247, Faculté de Pharmacie, F-34093, Montpellier cedex 5, France.
Institut des Biomolécules Max Mousseron-IBMM, Centre National de la Recherche Scientifique, Université de Montpellier 1, Université de Montpellier 2, Unité Mixte de Recherche 5247, Faculté de Pharmacie, F-34093, Montpellier cedex 5, France.
J Chromatogr A. 2015 Jan 9;1376:159-66. doi: 10.1016/j.chroma.2014.12.029. Epub 2014 Dec 12.
This work aims at studying the potentialities of an on-line capillary electrophoresis (CE)-based digestion methodology for evaluating polymer-drug conjugates degradability in the presence of free trypsin (in-solution digestion). A sandwich plugs injection scheme with transverse diffusion of laminar profile (TDLFP) mode was used to achieve on-line digestions. Electrophoretic separation conditions were established using poly-l-Lysine (PLL) as reference substrate. Comparison with off-line digestion was carried out to demonstrate the feasibility of the proposed methodology. The applicability of the on-line CE-based digestion methodology was evaluated for two PLL-drug conjugates and for the four first generations of dendrigraft of lysine (DGL). Different electrophoretic profiles presenting the formation of di, tri, and tetralysine were observed for PLL-drug and DGL. These findings are in good agreement with the nature of the linker used to link the drug to PLL structure and the predicted degradability of DGL. The present on-line methodology applicability was also successfully proven for protein conjugates hydrolysis. In summary, the described methodology provides a powerful tool for the rapid study of biodegradable polymers.
本研究旨在探讨基于在线毛细管电泳(CE)的消化方法在评估聚合物-药物共轭物在游离胰蛋白酶存在下(溶液中消化)的降解能力方面的潜力。采用具有层流剖面横向扩散(TDLFP)模式的夹心塞进样方案实现在线消化。以聚-L-赖氨酸(PLL)作为参考底物建立电泳分离条件。通过与离线消化进行比较,证明了所提出方法的可行性。对两种PLL-药物共轭物和赖氨酸的四代树枝状接枝聚合物(DGL)评估了基于在线CE的消化方法的适用性。对于PLL-药物和DGL,观察到呈现二赖氨酸、三赖氨酸和四赖氨酸形成的不同电泳图谱。这些发现与用于将药物连接到PLL结构的连接子的性质以及DGL的预测降解能力高度一致。所描述的在线方法在蛋白质共轭物水解方面的适用性也得到了成功验证。总之,所描述的方法为快速研究可生物降解聚合物提供了一个强大的工具。