Department of Chemistry , Penn State University , University Park , State College , Pennsylvania 16802 , United States.
Department of Biochemistry and Molecular Biology , Penn State University , State College , Pennsylvania 16802 , United States.
Langmuir. 2018 Sep 11;34(36):10782-10792. doi: 10.1021/acs.langmuir.8b01878. Epub 2018 Aug 27.
Ibuprofen (IBU) interacts with phosphatidylcholine membranes in three distinct steps as a function of concentration. In a first step (<10 μM), IBU electrostatically adsorbs to the lipid headgroups and gradually decreases the interfacial potential. This first step helps to facilitate the second step (10-300 μM), in which hydrophobic insertion of the drug occurs. The second step disrupts the packing of the lipid acyl chains and expands the area per lipid. In a final step, above 300 μM IBU, the lipid membrane begins to solubilize, resulting in a detergent-like effect. The results described herein were obtained by a combination of fluorescence binding assays, vibrational sum frequency spectroscopy, and Langmuir monolayer compression experiments. By introducing trimethylammonium-propane, phosphatidylglycerol, and phosphatidylethanolamine lipids as well as cholesterol, we demonstrated that both the chemistry of the lipid headgroups and the packing of lipid acyl chains can substantially influence the interactions between IBU and the membranes. Moreover, different membrane chemistries can alter particular steps in the binding interaction.
布洛芬(IBU)与磷脂膜相互作用分为三个不同的步骤,这取决于浓度。在第一步(<10 μM)中,IBU 静电吸附到脂质头部基团并逐渐降低界面电位。这第一步有助于促进第二步(10-300 μM),药物发生疏水性插入。第二步破坏了脂质酰基链的堆积并扩展了每个脂质的面积。在第三步(超过 300 μM IBU),脂质膜开始溶解,产生类似于去污剂的效果。本文的结果是通过荧光结合测定、振动和频光谱以及 Langmuir 单层压缩实验的组合获得的。通过引入三甲铵丙烷、磷脂酰甘油和磷脂酰乙醇胺脂质以及胆固醇,我们证明了脂质头部基团的化学性质和脂质酰基链的堆积都可以极大地影响 IBU 与膜之间的相互作用。此外,不同的膜化学性质可以改变结合相互作用的特定步骤。