Evidence map›Paper›PMID 28792093›Full record

ArticleRapid communications in mass spectrometry : RCM2017

Polymer-spray mass spectrometric detection and quantitation of hydrophilic compounds and some narcotics.

Maria T Dulay, Richard N Zare

Abstract read
In one paragraph

Article in Rapid communications in mass spectrometry : RCM, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Introducing Nafion forFrontiers in chemistry · 2021
    Article
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  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Maria T DulayDepartment of Chemistry, Stanford University, Stanford, CA, 94305, USA.ORCID http://orcid.org/0000-0002-4678-3480
Richard N ZareDepartment of Chemistry, Stanford University, Stanford, CA, 94305, USA.ORCID http://orcid.org/0000-0001-5266-4253

Funding

Ligand-Receptor Dynamics and Cellular Responses Studied In Situ Using Venturi Easy Ambient Sonic-Spray Ionization Mass SpectrometryR01MH112188 · NIMH · STANFORD UNIVERSITY · PI ZARE, RICHARD N · 2017 to 2019
$348k
Novel Silica-Based Organic Polymer for Ambient Ionization Mass SpectrometryR41GM113337 · NIGMS · PROSOLIA, INC. · PI WISEMAN, JUSTIN MICHAEL · 2015 to 2015
$162k
NIGMS NIH HHS R41 GM113337NIMH NIH HHS R01 MH112188
6 · The paper itself

Abstract

rationaleHigh-throughput screening of biofluids is essential in monitoring concentration of a variety of drugs to determine their efficacy and toxicity. Organosiloxane polymers prepared by sol-gel chemistry as sample supports, and electrospray ionization emitters in a single material and as an alternative to paper substrates, is described in this study.

methodsHydrophobic drugs and hydrophilic streptomycin were analyzed by polymer-spray mass spectrometry with an LTQ-Orbitrap mass spectrometer. Drug samples in urine (1-2 μL) were deposited on an OSX polymer, allowed to dry, then electrosprayed from the polymer tip into the mass spectrometer without sample pretreatment. The OSX polymers, whose polarity and porosity can be controlled, were prepared by sol-gel chemistry where methyl-substituted alkoxysilanes were hydrolyzed in the presence of a pore template and an acid catalyst.

resultsFive nanograms each of seven narcotic drugs were detected in <1 min (relative standard deviation (RSD) of response <1% for each drug). Calibration curves of cocaine and streptomycin in urine were used to establish the performance of the polymer. For sample 1 (n = 2), the mean recovery for cocaine was 81% with paper and 90% with polymer. Streptomycin is detected with polymer, not with paper; for samples 1 and 2 (n = 3), mean recovery was 97% and 95%, respectively.

conclusionsOrganosiloxane polymers achieve more sensitive analysis than paper, allowing for more accurate quantitation of both hydrophobic and hydrophilic drug compounds. The ability to tailor the polymer polarity and porosity allows for the synthesis of a wide range of polymers, and thus opens many possibilities for further development and applications.

Indexed as

Anesthetics, LocalAnti-Bacterial AgentsCocaineEquipment DesignHumansHydrophobic and Hydrophilic InteractionsMass SpectrometryNarcoticsPharmaceutical PreparationsPorositySiloxanesStreptomycinSubstance Abuse DetectionAnesthetics, LocalAnti-Bacterial AgentsCocaineNarcoticsPharmaceutical PreparationsSiloxanesStreptomycin

Identifiers

PMID28792093
PMCPMC5591076

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Registered trials

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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.