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Sigma-Aldrich

Straight channel chip (4 parallel channels)

Fluidic 156, PMMA

Synonym(s):

Microfluidic chip

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About This Item

UNSPSC Code:
42142600
NACRES:
NA.23

description

Microfludic chip x1

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Application

Straight channel chip (4 parallel channels), Fluidic 156, PMMA is the same dimensions of a microscope slide (75.5 mm x 25.5 mm x 1.5 mm). The channel distance from center to center is 4.5 mm according to the spacing of a 384-microtiter plate. The fluidic chips are available with Mini Luer interfaces that can be used with the respective counterpart. Alternatively, standard Luer interfaces are convenient. Channels can be orientated crosswise or lengthwise on the chip.

Chip Properties:
  • 4 parallel channels
  • Mini Luer Interface
  • Material: Poly(methyl methacrylate) (PMMA)
  • Slide Dimensions: 75.5 mm x 25.5 mm x 1.5 mm
  • Channel to channel distance: 4.5mm
  • Channel Dimensions: 200μm (width) x 200μm (depth) x 58.5mm (length)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Microfluidic-assisted fabrication of carriers for controlled drug delivery.
Santos H A, et al
Lab on a chip, 17, 1856-1883 (2017)
Recent advances of controlled drug delivery using microfluidic platforms.
Li X, et al.
Advanced Drug Delivery Reviews, 128, 3-28 (2018)
Microfluidic-assisted fabrication of carriers for controlled drug delivery.
Santos H A, et al.
Lab on a chip, 17, 1856-1883 (2017)
Sharma T Sanjay et al.
Advanced drug delivery reviews, 128, 3-28 (2017-09-19)
Conventional systematically-administered drugs distribute evenly throughout the body, get degraded and excreted rapidly while crossing many biological barriers, leaving minimum amounts of the drugs at pathological sites. Controlled drug delivery aims to deliver drugs to the target sites at desired
Dongfei Liu et al.
Lab on a chip, 17(11), 1856-1883 (2017-05-10)
The microfluidic technique has brought unique opportunities toward the full control over the production processes for drug delivery carriers, owing to the miniaturisation of the fluidic environment. In comparison to the conventional batch methods, the microfluidic setup provides a range

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