Haginaka J, Sakai Y
Faculty of Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya, Hyogo, Japan.
J Pharm Biomed Anal. 2000 Jul;22(6):899-907. doi: 10.1016/s0731-7085(00)00293-4.
A uniform-sized molecularly imprinted polymer for (S)-propranolol has been prepared by a multi-step swelling and thermal polymerization method using methacrylic acid (MAA) and ethylene glycol dimethacrylate (EDMA) as a host functional monomer and cross-linker, respectively. The obtained (S)-propranolol imprinted MAA-EDMA materials were evaluated using aqueous-rich eluents by HPLC. The (S)-propranolol imprinted MAA-EDMA materials had specific recognition for (S)-propranolol and moderate recognition for some structurally related beta-adrenergic antagonists (especially, pindolol and alprenolol), but had no recognition for other basic compounds, and neutral and acidic compounds. Enantioseparations of propranolol and some structurally related beta-adrenergic antagonists were attained with the imprinted MAA-EDMA materials. Hydrophobic interaction of the naphthyloxy and isopropyl groups of propranolol, and ionic interaction of the isopropylamino group of propranolol with the (S)-propranolol imprinted MAA-EDMA materials could play an important role in enantioselective recognition of propranolol.
通过多步溶胀和热聚合法,分别以甲基丙烯酸(MAA)和乙二醇二甲基丙烯酸酯(EDMA)作为主体功能单体和交联剂,制备了一种用于(S)-普萘洛尔的尺寸均匀的分子印迹聚合物。使用富含水的洗脱剂通过高效液相色谱法对所制备的(S)-普萘洛尔印迹的MAA-EDMA材料进行了评估。(S)-普萘洛尔印迹的MAA-EDMA材料对(S)-普萘洛尔具有特异性识别,对一些结构相关的β-肾上腺素能拮抗剂(尤其是吲哚洛尔和阿普洛尔)具有适度识别,但对其他碱性化合物、中性化合物和酸性化合物无识别作用。使用印迹的MAA-EDMA材料实现了普萘洛尔和一些结构相关的β-肾上腺素能拮抗剂的对映体分离。普萘洛尔的萘氧基和异丙基的疏水相互作用,以及普萘洛尔的异丙氨基与(S)-普萘洛尔印迹的MAA-EDMA材料的离子相互作用,在普萘洛尔的对映体选择性识别中可能起重要作用。