Markovich R J, Qiu X X, Nichols D E, Pidgeon C, Invergo B, Alvarez F M
Department of Medicinal Chemistry, Purdue University, West Lafayette, Indiana 47907.
Anal Chem. 1991 Sep 1;63(17):1851-60. doi: 10.1021/ac00017a034.
The silica surface of immobilized artificial membranes containing phosphatidylcholine (IAM.PC) has approximately two aminopropyl groups per immobilized phosphatidylcholine molecule. Primary amines near the silica subsurface adsorb biomolecules and also decrease the chemical stability of IAM.PC surfaces. Consequently, subsurface amines were end-capped by several methods including silylating reagents, acetyl analogues, glycidol, methyl glycolate, short-chain anhydrides (3-6 carbons/anhydride chain), and long-chain anhydrides (10-12 carbons/anhydride chain). All end-capping reactions resulted in loss of the initially immobilized phosphatidylcholine molecule. However, the amount of PC loss during end capping was very low (for alkyl anhydride end-capping reactions) to very high (for silylation end-capping reactions). After end capping, IAM.PC showed increased chemical stability compared to non end-capped IAM.PC surfaces. The chemical stability of IAM packing material was monitored by phospholipid leaching from IAM surfaces exposed to organic and aqueous solvents using thin-layer chromatography, 1H NMR spectroscopy, infrared spectroscopy, and mass spectrometry. IAM.PC packing material end capped with long-chain anhydrides exhibited the greatest chemical stability, i.e., little or no detectable phospholipid leaching when challenged with aqueous and/or organic solvents. The chromatography of acidic and basic compounds on end-capped and non-end-capped IAM.PC surfaces was studied. Compared to non-end-capped IAM.PC HPLC columns, the chromatographic retention times of acidic compounds (deoxynucleotides) decreased after end capping. In contrast, the retention times of basic compounds (amphetamine analogues) increased on end-capped IAM.PC HPLC columns relative to non-end-capped IAM.PC HPLC columns. This indicates that these solutes have access to the silica subsurface amines during chromatography.
含有磷脂酰胆碱的固定化人工膜(IAM.PC)的二氧化硅表面,每个固定化的磷脂酰胆碱分子大约有两个氨丙基。二氧化硅次表面附近的伯胺会吸附生物分子,同时也会降低IAM.PC表面的化学稳定性。因此,通过多种方法对次表面胺进行封端,包括硅烷化试剂、乙酰类似物、缩水甘油、乙醇酸甲酯、短链酸酐(每个酸酐链含3 - 6个碳)和长链酸酐(每个酸酐链含10 - 12个碳)。所有的封端反应都会导致最初固定化的磷脂酰胆碱分子损失。然而,封端过程中磷脂酰胆碱的损失量从非常低(对于烷基酸酐封端反应)到非常高(对于硅烷化封端反应)不等。封端后,与未封端的IAM.PC表面相比,IAM.PC的化学稳定性有所提高。通过使用薄层色谱、¹H核磁共振光谱、红外光谱和质谱法,监测暴露于有机溶剂和水性溶剂的IAM表面磷脂的浸出情况,以此来评估IAM填充材料的化学稳定性。用长链酸酐封端的IAM.PC填充材料表现出最大的化学稳定性,即在受到水性和/或有机溶剂挑战时,几乎没有或无法检测到磷脂浸出。研究了酸性和碱性化合物在封端和未封端的IAM.PC表面上的色谱行为。与未封端的IAM.PC高效液相色谱柱相比,封端后酸性化合物(脱氧核苷酸)的色谱保留时间缩短。相反,与未封端的IAM.PC高效液相色谱柱相比,碱性化合物(苯丙胺类似物)在封端后的IAM.PC高效液相色谱柱上的保留时间增加。这表明在色谱过程中,这些溶质能够接触到二氧化硅次表面的胺。