Evidence map›Paper›PMID 31592185›Full record

ArticleRSC advances2018

Click Chemistry Approaches to Expand the Repertoire of PEG-based Fluorinated Surfactants for Droplet Microfluidics.

Randall Scanga, Lucie Chrastecka, Ridhwan Mohammad, Austin Meadows, Phenix-Lan Quan, Eric Brouzes

Erratum issuedAbstract read
In one paragraph

Article in RSC advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. A Robust Synthesis of Fluorosurfactants with Tunable Functionalities via a Two-Step Reaction.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  3. Non-Ionic Fluorosurfactants for Droplet-Based in vivo Applications.Angewandte Chemie (International ed. in English) · 2024
    Article
  4. Article
  5. Resistivity detection of perfluoroalkyl substances with fluorous polyaniline in an electrical lateral flow sensor.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Randall ScangaDepartment of chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Lucie ChrasteckaDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York, USA.
Ridhwan MohammadDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York, USA.
Austin MeadowsDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York, USA.
Phenix-Lan QuanDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York, USA.
Eric BrouzesDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, New York, USA.

Funding

Multiparameter single-cell genomics platform for personalized treatment of cancerR01CA181595 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI BROUZES, ERIC · 2014 to 2018
$2.7M
NCI NIH HHS R01 CA181595
6 · The paper itself

Abstract

We report the novel and simplified synthesis of fluorinated surfactants for droplet microfluidics. The range of applications of droplet microfluidics has greatly expanded during the last decade thanks to its ability to manipulate and process tiny amount of sample and reagents at high throughput in independent reactors. A critical component of the technology is the formulation of the immiscible oil phase that contains surfactants to stabilize droplets. The success of droplet microfluidics relies mostly on a single fluorinated formulation that uses a PFPE-PEG tri-block surfactant. The synthesis of this surfactant is laborious and requires skills in synthetic chemistry preventing the wider community to explore the synthesis of alternate surfactants. We sought to provide a simplified synthesis for novel PFPE-PEG surfactants based on click chemistry approaches such as copper-catalyzed azide-alkyne cycloaddition (CuAAC) and UV-activated thiol-yne reactions. Our strategy is based on converting a moisture sensitive intermediate typically used in the synthesis of the tri-block PFPE-PEG surfactant into a stable and click ready molecule. We successfully combined that fluorinated tail with differently functionalized PEG and glycerol ethoxylate molecules to generate surfactants with diverse structures

Indexed as

click chemistrydroplet microfluidicsdropletsfluorinated surfactantssurfactants

Identifiers

PMID31592185
PMCPMC6779154

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.