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917494

Sigma-Aldrich

NanoFabTx device accessory

tubing, 250 μm FEP, 10 m, with ferrules

Synonym(s):

Microfluidic kit, NanoFabTx, Nanoformulation

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About This Item

UNSPSC Code:
41105100
NACRES:
NA.23

description

Microfludic hardware kit component: Tubing 10m, 250um FEP with ferrules x 1

Quality Level

application(s)

advanced drug delivery

General description

NanoFabTx device accessory, tubing, 250 μm FEP with ferrules, 10m is a component of our NanoFabTx microfluidic device kits (911593, 911860, 911879). The kits additionally include a protocol, manifold, and additional accessories for microfluidic-based synthesis. Fluorinated ethylene propylene (FEP) is a tough, flexible copolymer of tetrafluoroethylene and hexafluoropropylene, ideal for fluid processing equipment when chemical resistance, high purity, and low stiffness are required.

Application

NanoFabTx device accessory, tubing, 250 μm FEP with ferrules, 10m can be used as a replacement for the component in our NanoFabTx microfluidic device kits (911593, 911860, 911879).

Legal Information

NANOFABTX is a trademark of Sigma-Aldrich Co. LLC

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Andrew Gdowski et al.
Journal of nanobiotechnology, 16(1), 12-12 (2018-02-13)
The process of optimization and fabrication of nanoparticle synthesis for preclinical studies can be challenging and time consuming. Traditional small scale laboratory synthesis techniques suffer from batch to batch variability. Additionally, the parameters used in the original formulation must be
Xuanyu Li et al.
Advanced drug delivery reviews, 128, 101-114 (2017-12-27)
Microfluidic chips allow the rapid production of a library of nanoparticles (NPs) with distinct properties by changing the precursors and the flow rates, significantly decreasing the time for screening optimal formulation as carriers for drug delivery compared to conventional methods.
Samar Damiati et al.
Genes, 9(2) (2018-02-22)
Microfluidic devices present unique advantages for the development of efficient drug carrier particles, cell-free protein synthesis systems, and rapid techniques for direct drug screening. Compared to bulk methods, by efficiently controlling the geometries of the fabricated chip and the flow

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