ArticleTalanta2017
Capillary electrophoresis coupled to negative mode electrospray ionization-mass spectrometry using an electrokinetically-pumped nanospray interface with primary amines grafted to the interior of a glass emitter.
Article in Talanta, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed, 17 citations in OpenAlex.
- Capillary Electrophoresis-Mass Spectrometry for Cancer Metabolomics.Advances in experimental medicine and biology · 2021Article
- Investigation of electrospray for a capillary electrophoresis-mass spectrometry interface in reverse polarity and negative ion mode.European journal of mass spectrometry (Chichester, England) · 2019Article
- Dual cationic-anionic profiling of metabolites in a single identified cell in a live Xenopus laevis embryo by microprobe CE-ESI-MS.The Analyst · 2019Article
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
Abstract
We demonstrate an electrokinetically pumped sheath flow nanospray interface for capillary electrophoresis coupled to negative mode electrospray mass spectrometry. In this interface, application of an electric field generates electro-osmotic flow at the interior of a glass emitter that is pulled to a 10-20µm inner diameter orifice. Electro-osmotic flow pumps liquid around the distal tip of the separation capillary, ensheathing analyte into the electrospray electrolyte. In negative ion mode, negative potential applied to an untreated glass emitter drives sheath flow away from the emitter orifice, decreasing the stability and efficiency of the spray. In this manuscript, we treat a portion of the interior of the electrospray emitter with 3-aminopropyltrimethoxysilane, which grafts primary amines to the interior. The amines take on a positive charge, which reverses electro-osmosis and generates stable sheath flow to the emitter orifice under negative potential. Negative mode operation is demonstrated by analyzing a metabolite extract from stage 1 Xenopus laevis embryos. Production of the treated emitters was quite reproducible. We evaluated the performance of three emitters using a set of amino acids; the relative standard deviation in peak intensity was 7% for the most intense component.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.