Université de Lyon, CNRS, Laboratoire des Sciences Analytiques, 69622 Villeurbanne, France.
Rapid Commun Mass Spectrom. 2009 Nov;23(21):3409-22. doi: 10.1002/rcm.4268.
A second generation ionic liquid matrix (ILM), N,N-diisopropylethylammonium alpha-cyano-4-hydroxycinnamate (DEA-CHCA), was developed for the characterization of polar biodegradable polymers. It is compared with five solid matrices typically used for the characterization of these polymers and one other new ILM. It is shown that use of the ILM, DEA-CHCA, allows maximum signal with minimum laser intensity which minimizes polymer degradation. In these conditions, the DEA-CHCA ILM is able to assist in the ionization of analytes in an efficient but soft manner. These qualities produce spectra that allow an accurate and sensitive determination of the number average molecular weights, weight average m.w., and polydispersity index of labile polar polymers. With such polymers, many solid matrices produce spectra showing extensive polymer degradation leading to the underestimation of molecular weights. The distribution of intact analyte peaks obtained with the ILM DEA-CHCA allows for identification of the fine structure of complex copolymers. ILMs were much less susceptible to effects of extraction delay times on molecular weight determination than were solid matrices. The liquid nature of the matrix is an important reason for the outstanding results obtained for labile analyte polymers. No comparable results could be obtained with any known solid matrices or other ILMs. In many cases, the manufacturers' listed molecular weights and polydispersity measurements for biodegradable polymers are determined by size-exclusion chromatography and the data obtained by that method may differ considerably from the high-precision matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) results presented here.
第二代离子液体基质(ILM)N,N-二异丙基乙基氯化铵α-氰基-4-羟基肉桂酸(DEA-CHCA)被开发用于鉴定极性可生物降解聚合物。它与通常用于鉴定这些聚合物的五种固体基质和另一种新型 ILM 进行了比较。结果表明,使用 ILM,DEA-CHCA,可以在最小化聚合物降解的情况下用最小的激光强度获得最大的信号。在这些条件下,DEA-CHCA ILM 能够以有效但柔和的方式辅助分析物的电离。这些特性产生的光谱允许准确和灵敏地测定不稳定极性聚合物的数均分子量、重均分子量 m.w. 和多分散指数。对于此类聚合物,许多固体基质产生的光谱显示出广泛的聚合物降解,导致分子量低估。使用 ILM DEA-CHCA 获得的完整分析物峰的分布允许鉴定复杂共聚物的精细结构。ILM 对分子量测定的萃取延迟时间的影响比固体基质小得多。基质的液体性质是获得不稳定分析物聚合物出色结果的重要原因。任何已知的固体基质或其他 ILM 都无法获得可比的结果。在许多情况下,可生物降解聚合物的制造商列出的分子量和多分散性测量值是通过尺寸排阻色谱法确定的,并且该方法获得的数据可能与这里呈现的高精度基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)结果有很大差异。