Simple chip-based interfaces for on-line monitoring of supramolecular interactions by nano-ESI MS

Lab Chip. 2005 Oct;5(10):1111-22. doi: 10.1039/b510534j. Epub 2005 Aug 17.

Abstract

Two simple interfaces were designed and realized, enabling on-line coupling of microfluidics reactor chips to a nanoflow electrospray ionization (NESI) time-of-flight (TOF) mass spectrometer (MS). The interfaces are based on two different approaches: a monolithically integrated design, in which ionization is assisted by on-chip gas nebulization, and a modular approach implying the use of commercially available Picospray tips. Using reserpine as a reference compound in a 1ratio1 mixture of acetonitrile and water revealed that both interfaces provide a remarkably stable mass spectrometric signal (standard deviations lower than 8% and 1% for the monolithic and modular approaches, respectively). Glass microreactors, containing mixing zones, were fabricated and coupled to the modular interface with perfluoroelastomer Nanoport fluidics connectors, providing a tool to study chemical reactions on-line. Investigation of the mixing dynamics showed that complete on-chip reagents mixing is achieved within a few tens of milliseconds. Metal-ligand interactions of Zn-porphyrin with pyridine (2), 4-ethylpyridine (3), 4-phenylpyridine (4), N-methylimidazole (5), and N-butylimidazole (6) in acetonitrile as well as host-guest complexations of beta-cyclodextrin (7) with N-(1-adamantyl)acetamide (8) or 4-tert-butylacetanilide (9) in water were studied by mass spectrometry using the modular NESI-chip interface. From on-chip dilution-based mass spectrometric titrations of Zn-porphyrin 1 with pyridine (2) or 4-phenylpyridine (4) in acetonitrile Ka-values of 4.6 +/- 0.4 x 10(3) M(-1) and 6.5 +/- 1.2 x 10(3) M(-1), respectively, were calculated. The Ka-values are about four times larger than those obtained with UV/vis spectroscopy in solution, probably due to a higher ionization efficiency of complexed compared to uncomplexed Zn-porphyrin. For the complexation of N-(1-adamantyl)acetamide (8) with beta-cyclodextrin (7), a Ka-value of 3.6 +/- 0.3 x 10(4) M(-1) was obtained, which is in good agreement with that determined by microcalorimetry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetanilides / chemistry
  • Acetonitriles / chemistry
  • Amantadine / chemistry
  • Calorimetry
  • Electrophoresis, Capillary / methods
  • Electrophoresis, Microchip / methods
  • Gases
  • Imidazoles / chemistry
  • Ions
  • Kinetics
  • Ligands
  • Mass Spectrometry
  • Metals / chemistry
  • Microfluidic Analytical Techniques / instrumentation*
  • Microfluidic Analytical Techniques / methods*
  • Microscopy, Fluorescence
  • Models, Chemical
  • Nanotechnology
  • Porphyrins / chemistry
  • Protein Array Analysis / methods*
  • Pyridines / chemistry
  • Reserpine / pharmacology
  • Software
  • Spectrometry, Mass, Electrospray Ionization / instrumentation*
  • Spectrometry, Mass, Electrospray Ionization / methods*
  • Time Factors
  • Water / chemistry
  • Zinc / chemistry
  • beta-Cyclodextrins / chemistry

Substances

  • Acetanilides
  • Acetonitriles
  • Gases
  • Imidazoles
  • Ions
  • Ligands
  • Metals
  • Porphyrins
  • Pyridines
  • beta-Cyclodextrins
  • Water
  • 1-N-butylimidazole
  • 4-phenylpyridine
  • Reserpine
  • N-butylacetanilide
  • Amantadine
  • Zinc
  • betadex
  • pyridine
  • 1-methylimidazole
  • acetonitrile