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Key Documents

911917

Sigma-Aldrich

NanoFabTx™ microfluidic chip

for 100-200 nm particles

Synonyme(s) :

Microfluidic kit, NanoFabTx™, Nanoformulation

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About This Item

Code UNSPSC :
41116105
Code UNSPSC :
41121800
Nomenclature NACRES :
NA.23

Description

Microfludic hardware kit component for synthesizing nanoparticles

Kit components :

  • Microfluidic chip x 1

Niveau de qualité

100

Application(s)

advanced drug delivery

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Description générale

NanoFabTx™ microfluidic chip, for 100-200 nm particles is a component of our NanoFabTx™ microfluidic - nano, device kit for synthesis of 100-200 nm nanoparticles and liposomes (911593). The kit additionally includes a protocol, supporting manifold, tubing, and additional accessories for microfluidic-based synthesis.

Application

NanoFabTx™ microfluidic chips precisely control and manipulate fluids on the microscale. Their well-controlled geometries enable facile syntheses of monodisperse polymeric nanoparticles. NanoFabTx™ microfluidic chip, for 100-200 nm particles can be used as a replacement for the component in our NanoFabTx™ microfluidic - nano, device kit for synthesis of 100-200 nm nanoparticles and liposomes (911593).

Informations légales

NANOFABTX is a trademark of Sigma-Aldrich Co. LLC

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

911593

NanoFabTx™ microfluidic - nano, device kit for synthesis of 100-200 nm nanoparticles and liposomes

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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
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.
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

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