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911925

Sigma-Aldrich

NanoFabTx™ microfluidic chip

for 1-5 μm particles

Synonym(e):

Microfluidic kit, Microparticle, NanoFabTx™, Nanoformulation

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About This Item

UNSPSC-Code:
41116105
UNSPSC-Code:
41121800
NACRES:
NC.25

Beschreibung

Microfludic hardware kit component for synthesizing 1-5 μm microparticles

Kit components :

  • Microfluidic chip x 1

Qualitätsniveau

100

Anwendung(en)

advanced drug delivery

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Allgemeine Beschreibung

NanoFabTx™ microfluidic chip, for 1-5 μm particles is a component of our NanoFabTx™ microfluidic - micro, device kit for synthesis of 1-5 µm particles (911860). The kit additionally includes a protocol, supporting manifold, tubing, and additional accessories for microfluidic-based synthesis.

Anwendung

NanoFabTx™ microfluidic chips precisely control and manipulate fluids on the microscale. Their well-controlled geometries enable facile syntheses of monodisperse polymeric microparticles. NanoFabTx™ microfluidic chip, for 1-5 μm particles can be used as a replacement for the component in our NanoFabTx™ microfluidic - micro, device kit for synthesis of 1-5 μm particles (911860).

Rechtliche Hinweise

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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