Segro Scott S, Malik Abdul
Department of Chemistry, University of South Florida, 4202 E. Fowler Avenue, CHE 205, Tampa, FL 33620-5250, USA.
J Chromatogr A. 2009 Nov 6;1216(45):7677-86. doi: 10.1016/j.chroma.2009.09.030. Epub 2009 Sep 16.
Fused silica capillaries with surface-bonded sol-gel coatings containing covalently attached octadecyl, octyl, and methyl groups were prepared for capillary microextraction (CME) hyphenated on-line with high-performance liquid chromatography (HPLC). For this, octadecyltrimethoxysilane (C(18)TMS), octyltrimethoxysilane (C(8)TMS), or methyltrimethoxysilane (MTMS) was used as the respective sol-gel precursor. Hydrolytic polycondensation of these precursors led to the formation of surface-bonded sol-gel sorbents with pendant alkyl groups ready to serve as the extraction medium; no additional surface derivatization reactions were needed to anchor these ligands to the surface. Extraction behaviors of two sets of microextraction capillaries with alkyl-bonded sol-gel coatings were investigated: (a) capillaries prepared with a constant molar concentration of these precursors in the sol solution, and (b) capillaries prepared with varied molar concentrations of C(8)TMS in the sol solution. Among the capillaries prepared using sol solutions with the same molar concentration of sol-gel precursor, the detection limits for nonpolar and polar analytes ranged from 0.3ng/L to 213.9ng/L. The sol-gel octadecyl-coated capillaries were found to be the most efficient at extracting these analytes, followed by the sol-gel octyl-coated capillaries, followed by the sol-gel methyl-coated capillaries. The results of this study point to the possibility that polar analytes are extracted through synergistic molecular level interactions of the polar and nonpolar parts of the analyte molecules with the alkyl chains and silanol groups within the sol-gel coatings. These coatings also demonstrated run-to-run and capillary-to-capillary reproducibility, with HPLC peak area RSD values ranging from 1.1% to 9.6% and 1.3% to 10.0%, respectively. In the set of sol-gel octyl capillaries with varied molar concentrations, the capillaries prepared with 0.514M concentration of C(8)TMS in the sol solution were most efficient in extracting nonpolar and polar analytes. When higher or lower concentrations of C(8)TMS were used in the sol solution, the resulting sol-gel coated capillaries were less efficient in extracting nonpolar and polar analytes.
制备了具有表面键合溶胶 - 凝胶涂层的熔融石英毛细管,该涂层含有共价连接的十八烷基、辛基和甲基基团,用于与高效液相色谱(HPLC)在线联用的毛细管微萃取(CME)。为此,分别使用十八烷基三甲氧基硅烷(C(18)TMS)、辛基三甲氧基硅烷(C(8)TMS)或甲基三甲氧基硅烷(MTMS)作为溶胶 - 凝胶前体。这些前体的水解缩聚导致形成具有侧链烷基的表面键合溶胶 - 凝胶吸附剂,可作为萃取介质;无需额外的表面衍生化反应将这些配体锚定到表面。研究了两组具有烷基键合溶胶 - 凝胶涂层的微萃取毛细管的萃取行为:(a)在溶胶溶液中使用这些前体的恒定摩尔浓度制备的毛细管,以及(b)在溶胶溶液中使用不同摩尔浓度的C(8)TMS制备的毛细管。在使用具有相同摩尔浓度溶胶 - 凝胶前体的溶胶溶液制备的毛细管中,非极性和极性分析物的检测限范围为0.3ng/L至213.9ng/L。发现溶胶 - 凝胶十八烷基涂层毛细管在萃取这些分析物方面效率最高,其次是溶胶 - 凝胶辛基涂层毛细管,然后是溶胶 - 凝胶甲基涂层毛细管。该研究结果表明,极性分析物可能通过分析物分子的极性和非极性部分与溶胶 - 凝胶涂层内的烷基链和硅醇基团之间的协同分子水平相互作用进行萃取。这些涂层还表现出批间和毛细管间的重现性,HPLC峰面积的相对标准偏差(RSD)值分别为1.1%至9.6%和1.3%至10.0%。在具有不同摩尔浓度的溶胶 - 凝胶辛基毛细管组中,在溶胶溶液中使用浓度为0.514M的C(8)TMS制备的毛细管在萃取非极性和极性分析物方面效率最高。当在溶胶溶液中使用更高或更低浓度的C(8)TMS时,所得的溶胶 - 凝胶涂层毛细管在萃取非极性和极性分析物方面效率较低。