Capillary electrochromatography with packed bead beds in microfluidic devices

Electrophoresis - Tập 30 Số 24 - Trang 4237-4244 - 2009
Abebaw B. Jemere1, Dolores Barranco Martínez2, Michael Finot2, D. Jed Harrison3,4
1National Institute for Nanotechnology, National Research Council Canada, Edmonton,#N#Alberta,#N#Canada
2Department of Chemistry, University of Alberta, Edmonton, Alberta Canada
3Department of Chemistry, University of Alberta, Edmonton, Alberta,#N#Canada#N#
4National Institute for Nanotechnology, National Research Council Canada, Edmonton, Alberta, Canada

Tóm tắt

Abstract

Microchip‐based bead‐packed columns for electrochromatography are described for several types of stationary phases. Chromatography columns 2 mm in length were used for the separation of proteins and peptides by size‐ and ion‐exchange modes of separation, respectively. In size‐exclusion electrochromatograpgy, FITC‐IgG and FITC‐insulin were baseline resolved in less than 10 s, with efficiencies of up to 139,000 plates/m for FITC‐insulin. In strong cation‐exchange electrochromatography, a mixture of three fluorescently labeled peptides was baseline resolved in less than 40 s, with efficiencies up to 400,000 plates/m. The RSD for the analytes retention times were<3% in both size‐exclusion and ion‐exchange modes of separations. The use of a 1‐mm‐long reverse‐phase column for the semiquantitative evaluation of pharmaceutical formulations in drug solubility tests illustrates the use of this microfluidic chip‐based electrochromatographic approach to drug development.

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Tài liệu tham khảo

10.1002/1522-2683(200012)21:18<3931::AID-ELPS3931>3.0.CO;2-M

10.1021/ac9606620

10.1002/elps.1150181211

10.1126/science.261.5123.895

10.1021/ac00041a030

10.1021/ac00079a028

10.1002/elps.1150160179

10.1073/pnas.91.24.11348

10.1016/S0021-9673(00)82057-9

10.1016/S0021-9673(98)00142-3

10.1016/S0021-9673(99)01328-X

10.1021/ac9811470

10.1016/S0021-9673(96)00864-3

10.1021/ac000114t

10.1016/S0021-9673(97)00626-2

10.1021/ac970626g

10.1016/S0021-9673(00)00460-X

10.1002/1522-2683(200111)22:19<4064::AID-ELPS4064>3.0.CO;2-9

10.1021/ac001019n

10.1002/elps.200305609

10.1016/S0021-9673(02)01739-9

10.1021/ac011077o

Svec F., 2003, LC GC Europe, 16, 24

10.1002/elps.200305538

10.1002/1522-2683(200210)23:20<3537::AID-ELPS3537>3.0.CO;2-9

10.1021/ac990751n

10.1021/ac00073a029

10.1016/S0925-4005(00)00351-8

10.1016/S0021-9673(99)00081-3

10.1021/ac00058a029

10.1039/a800153g

10.1016/0021-9673(92)85455-3

10.1021/ac971260a

10.1007/BF02495322

10.1021/ac991009q

10.1002/1522-2683(200205)23:9<1217::AID-ELPS1217>3.0.CO;2-C

10.1002/(SICI)1522-2683(20000401)21:7<1395::AID-ELPS1395>3.0.CO;2-C

10.1007/BF02467702

10.1093/clinchem/44.3.591

10.1016/S0021-9673(01)01601-6

10.1016/S0021-9673(99)01215-7

10.1016/S0021-9673(99)00076-X

10.1016/S0021-9673(00)88456-3

Voet D., 1995, Biochemistry

10.1016/S0021-9673(00)82234-7

10.1016/S0021-9673(01)92076-X

10.1016/S0021-9673(01)00709-9

10.1021/ac001302m

10.1002/(SICI)1521-4168(20000501)23:5<373::AID-JHRC373>3.0.CO;2-Z

10.1016/S0021-9673(99)01192-9

10.1021/bi982161

10.1021/bi981704c

10.1021/ac00086a024