de Koster C G, Duursma M C, van Rooij G J, Heeren R M, Boon J J
Unit for Macromolecular Mass Spectrometry, FOM Institute for Atomic and Molecular Physics, Amsterdam, The Netherlands.
Rapid Commun Mass Spectrom. 1995;9(10):957-62. doi: 10.1002/rcm.1290091018.
Fourier-transform ion cyclotron resonance mass spectrometry (FTICR-MS) by external injection of matrix-assisted laser desorbed and ionized (MALDI) polymers offers good possibilities for characterization of low molecular weight homopolymers (MW range up to 10 kDa). The molecular masses of the molecular weight distribution (MWD) components of underivatized and derivatized (dimethyl, dipropyl, dibutyl and diacetyl) polyethylene glycol (PEG) 1000 and 4000 were measured by MALDI-FTICR-MS. These measurements have been performed using a commercial FTICR spectrometer with a home-built external ion source. MALDI of the samples with a 2,5-dihydroxybenzoic acid matrix in a 1000:1 matrix-to-analyte molar ratio produces sodiated molecules in a sufficient yield to trap the ions in the ICR cell. The masses of the molecular weight distribution of PEG components were measured in broad-band mode with a mass accuracy of < 5 ppm in the mass range around 1000 u and within 40 ppm accuracy around 4000 u. From these measurements, the endgroup mass of the polymer was determined by correlation of the measured component mass with the degree of polymerization. The masses of the PEG endgroups have been determined within a deviation of 3-10 millimass units for the PEG1000 derivatives and 10-100 millimass units for the PEG4000 derivatives, thus confirming the identity of the distal parts of the model compounds.
通过外部注入基质辅助激光解吸电离(MALDI)聚合物的傅里叶变换离子回旋共振质谱(FTICR-MS)为表征低分子量均聚物(分子量范围高达10 kDa)提供了良好的可能性。通过MALDI-FTICR-MS测量了未衍生化和衍生化(二甲基、二丙基、二丁基和二乙酰基)的聚乙二醇(PEG)1000和4000的分子量分布(MWD)组分的分子量。这些测量是使用带有自制外部离子源的商用FTICR光谱仪进行的。在1000:1的基质与分析物摩尔比下,用2,5-二羟基苯甲酸基质对样品进行MALDI,能以足够的产率产生钠化分子,以便将离子捕获在ICR池中。在宽带模式下测量PEG组分的分子量分布,在1000 u左右的质量范围内质量准确度<5 ppm,在4000 u左右的质量范围内准确度在40 ppm以内。通过将测量的组分质量与聚合度相关联,从这些测量中确定了聚合物的端基质量。对于PEG1000衍生物,PEG端基的质量测定偏差在3 - 10毫质量单位以内,对于PEG4000衍生物,偏差在10 - 100毫质量单位以内,从而证实了模型化合物末端部分的身份。