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Merck
CN
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安全信息

911925

Sigma-Aldrich

NanoFabTx microfluidic chip

for 1-5 μm particles

别名:

Microfluidic kit, Microparticle, NanoFabTx, Nanoformulation

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About This Item

UNSPSC代码:
41116105
UNSPSC代码:
41121800
NACRES:
NC.25

描述

Microfludic hardware kit component for synthesizing 1-5 μm microparticles

Kit components :

  • Microfluidic chip x 1

质量水平

应用

advanced drug delivery

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一般描述

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.

应用

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).

法律信息

NANOFABTX is a trademark of Sigma-Aldrich Co. LLC

法规信息

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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
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.

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