TY - CHAP
T1 - Hollow-fiber flow field-flow fractionation
T2 - A pipeline to scale down separation and enhance detection of proteins and cells
AU - Reschiglian, Pierluigi
AU - Zattoni, Andrea
AU - Roda, Barbara
AU - Rambaldi, Diana C.
AU - Moon, Myeong Hee
N1 - Publisher Copyright:
© 2012 Springer-Verlag/Wien.
PY - 2012/1/1
Y1 - 2012/1/1
N2 - Commercial flow field-flow fractionation (FlFFF) employs macro-scale, flat-type channels. The idea of hollow-fiber (HF) membranes as tubular, micro-column channels for FlFFF (HF FlFFF or, more shortly, HF5) dates back to 1974, with fundamentals on HF5 given in the late 1980s, and outstanding applications reported only over the last 15 years.Compared to flat-channel FlFFF, the key aspect of HF5 lies in the downscaling of the fractionation channel. This implies low-cost, possible disposable usage, and low volume of the channel that allows on-line coupling with highly sensitive detection and characterization techniques. The use of coupled techniques enhances the analysis of macromolecules and micron-sized particles such as intact proteins and whole cells. In this chapter we first report a few basics on HF5 theory and instrumentation. We then focus on technical and methodological developments that have made HF5 reach a performance normally achieved by flat-channel FlFFF. We finally focus on the enhancements obtained by coupling HF5 with powerful methods for detection and characterization of intact proteins and whole cells such as multi-angle light scattering (MALS), time-of-flight (TOF) mass spectrometry (MS), chemiluminescence (CL), and UV/Vis turbidity diode-array detection (DAD).
AB - Commercial flow field-flow fractionation (FlFFF) employs macro-scale, flat-type channels. The idea of hollow-fiber (HF) membranes as tubular, micro-column channels for FlFFF (HF FlFFF or, more shortly, HF5) dates back to 1974, with fundamentals on HF5 given in the late 1980s, and outstanding applications reported only over the last 15 years.Compared to flat-channel FlFFF, the key aspect of HF5 lies in the downscaling of the fractionation channel. This implies low-cost, possible disposable usage, and low volume of the channel that allows on-line coupling with highly sensitive detection and characterization techniques. The use of coupled techniques enhances the analysis of macromolecules and micron-sized particles such as intact proteins and whole cells. In this chapter we first report a few basics on HF5 theory and instrumentation. We then focus on technical and methodological developments that have made HF5 reach a performance normally achieved by flat-channel FlFFF. We finally focus on the enhancements obtained by coupling HF5 with powerful methods for detection and characterization of intact proteins and whole cells such as multi-angle light scattering (MALS), time-of-flight (TOF) mass spectrometry (MS), chemiluminescence (CL), and UV/Vis turbidity diode-array detection (DAD).
KW - Chemiluminescence
KW - Detection
KW - FlFFF
KW - Flow field-flow fractionation
KW - HF FlFFF
KW - HF5
KW - High-molar mass protein separation
KW - Hollow fiber flow field-flow fractionation
KW - Light scattering
KW - Mass spectrometry
KW - Miniaturized channel
KW - Turbidimetric detection
KW - Whole cell separation
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U2 - 10.1007/978-3-7091-0154-4_3
DO - 10.1007/978-3-7091-0154-4_3
M3 - Chapter
AN - SCOPUS:84912573769
SN - 9783709101537
SP - 37
EP - 56
BT - Field-Flow Fractionation in Biopolymer Analysis
PB - Springer-Verlag Wien
ER -