High-Resolution Peptide Mapping Separations with MS-Friendly Mobile Phases and Charge-Surface-Modified C18

Ionic analytes, such as peptides, can be challenging to separate by reverse-phase chromatography with optimal efficiency. They tend, for instance, to exhibit poor peak shapes, particularly when eluted with mobile phases preferred for electrospray ionization mass spectrometry. We demonstrate that a novel charged-surface C18 stationary phase alleviates some of the challenges associated with reverse-phase peptide separations. This column chemistry, known as CSH (charged-surface hybrid) C18, improves upon an already robust organosilica hybrid stationary phase, BEH (ethylene-bridged hybrid) C18. Based on separations of a nine-peptide standard, CSH C18 was found to exhibit improved loadability, greater peak capacities, and unique selectivity compared to BEH C18. Its performance was also seen to be significantly less dependent on TFA-ion pairing, making it ideal for MS applications where high sensitivity is desired. These performance advantages were evaluated through application to peptide mapping, wherein CSH C18 was found to aid the development of a high-resolution, high-sensitivity LC-UV-MS peptide mapping method for the therapeutic antibody, trastuzumab. From these results, the use of a C18 stationary phase with a charged surface, such as CSH C18, holds significant promise for facilitating challenging peptide analyses

Synthesis and Surface Chemistry of Spherical Mesoporous Organic−Inorganic Hybrid Particles with an Integrated Alcohol Functionality on the Pore Surface

Novel mesoporous organic−inorganic spherical hybrid particles are described that contain a 3-hydroxypropyl organic functionality which is integral to the pore surface. The 3-hydroxypropyl hybrid particle is synthesized in three steps starting from a 4:1 (mol/mol) mixture of tetraethoxysilane and [3-(methacryloxy)propyl]trimethoxysilane, where the monomers are polymerized to a poly(organoalkoxysilane) oil, followed by sol−gel reaction to the hybrid silicate bead, which is finally subjected to an alkaline hydrothermal treatment to liberate the alcohol from the ester protecting group. The silicate precursor and final product were characterized by NMR spectroscopy and nitrogen sorption analysis. The heterogeneous surface chemistry of the hybrid's alcohol functionality was explored by running a series of classical alcohol reactions including bromination, esterification (carbamic and carbonic), and etherification (Williamson, epoxide ring opening). The brominated analogue was further converted via cyanation and Grignard couplings. Nuances to the heterogeneous surface chemistry are discussed as well as product characterizations by NMR spectroscopy and combustion analysis. A stability study was further conducted on the 3-hydroxypropyl hybrid silicate using an alkaline resistance test under HPLC packed column conditions. The hybrid material was found to be over 10-fold more stable than a comparable silica gel material. In a second HPLC test, the cyano derivatized hybrid material was found to be more resistant to acid-induced siloxane cleavage vs a comparable (3-cyanopropyl)silane grafted silica gel

Characterization and Evaluation of C₁₈ HPLC Stationary Phases Based on Ethyl-Bridged Hybrid Organic/Inorganic Particles

The characterization and evaluation of three novel 5-μm HPLC column packings, prepared using ethyl-bridged hybrid organic/inorganic materials, is described. These highly spherical hybrid particles, which vary in specific surface area (140, 187, and 270 m2/g) and average pore diameter (185, 148, and 108 Å), were characterized by elemental analysis, SEM, and nitrogen sorption analysis and were chemically modified in a two-step process using octadecyltrichlorosilane and trimethylchlorosilane. The resultant bonded materials had an octadecyl surface concentration of 3.17−3.35 μmol/m2, which is comparable to the coverage obtained for an identically bonded silica particle (3.44 μmol/m2) that had a surface area of 344 m2/g. These hybrid materials were shown to have sufficient mechanical strength under conditions normally employed for traditional reversed-phase HPLC applications, using a high-pressure column flow test. The chromatographic properties of the C18 bonded hybrid phases were compared to a C18 bonded silica using a variety of neutral and basic analytes under the same mobile-phase conditions. The hybrid phases exhibited similar selectivity to the silica-based column, yet had improved peak tailing factors for the basic analytes. Column retentivity increased with increasing particle surface area. Elevated pH aging studies of these hybrid materials showed dramatic improvement in chemical stability for both bonded and unbonded hybrid materials compared to the C18 bonded silica phase, as determined by monitoring the loss in column efficiency through 140-h exposure to a pH 10 triethylamine mobile phase at 50 °C