Use of PLL-g-PEG in micro-fluidic devices for localizing selective and specific protein binding
(2006) In Langmuir 22(24). p.10103-10108- Abstract
- By utilizing flow-controlled PLL-g-PEG and PLL-g-PEGbiotin modification of predefined regions of a poly-(dimethylsiloxane) (PDMS) micro-fluidic device, with an intentionally chosen large (similar to 1 cm(2)) internal surface area, we report rapid (10 min), highly localized (6 x 10(-6) cm(2)), and specific surface-based protein capture from a sample volume (100 mu L) containing a low amount of protein (160 attomol in pure buffer and 400 attomol in serum). The design criteria for this surface modification were achieved using QCM-D (quartz crystal microbalance with energy dissipation monitoring) of serum protein adsorption onto PLL-g-PEG-modified oxidized PDMS. Equally good, or almost as good, results were obtained for oxidized SU-8, Topas,... (More)
- By utilizing flow-controlled PLL-g-PEG and PLL-g-PEGbiotin modification of predefined regions of a poly-(dimethylsiloxane) (PDMS) micro-fluidic device, with an intentionally chosen large (similar to 1 cm(2)) internal surface area, we report rapid (10 min), highly localized (6 x 10(-6) cm(2)), and specific surface-based protein capture from a sample volume (100 mu L) containing a low amount of protein (160 attomol in pure buffer and 400 attomol in serum). The design criteria for this surface modification were achieved using QCM-D (quartz crystal microbalance with energy dissipation monitoring) of serum protein adsorption onto PLL-g-PEG-modified oxidized PDMS. Equally good, or almost as good, results were obtained for oxidized SU-8, Topas, and poly(methyl metacrylate) (PMMA), demonstrating the generic potential of PLL-g-PEG for surface modification in various micro-fluidic applications. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/376914
- author
- Marie, Rodolphe LU ; Beech, Jason LU ; Voeroes, Janos ; Tegenfeldt, Jonas LU and Höök, Fredrik LU
- organization
- publishing date
- 2006
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Langmuir
- volume
- 22
- issue
- 24
- pages
- 10103 - 10108
- publisher
- The American Chemical Society (ACS)
- external identifiers
-
- wos:000242022100044
- scopus:33846121311
- pmid:17107006
- ISSN
- 0743-7463
- DOI
- 10.1021/la060198m
- language
- English
- LU publication?
- yes
- id
- 8c0875d3-e6a3-4816-8586-d59bf7dff685 (old id 376914)
- date added to LUP
- 2016-04-01 11:37:28
- date last changed
- 2024-08-20 11:37:36
@article{8c0875d3-e6a3-4816-8586-d59bf7dff685, abstract = {{By utilizing flow-controlled PLL-g-PEG and PLL-g-PEGbiotin modification of predefined regions of a poly-(dimethylsiloxane) (PDMS) micro-fluidic device, with an intentionally chosen large (similar to 1 cm(2)) internal surface area, we report rapid (10 min), highly localized (6 x 10(-6) cm(2)), and specific surface-based protein capture from a sample volume (100 mu L) containing a low amount of protein (160 attomol in pure buffer and 400 attomol in serum). The design criteria for this surface modification were achieved using QCM-D (quartz crystal microbalance with energy dissipation monitoring) of serum protein adsorption onto PLL-g-PEG-modified oxidized PDMS. Equally good, or almost as good, results were obtained for oxidized SU-8, Topas, and poly(methyl metacrylate) (PMMA), demonstrating the generic potential of PLL-g-PEG for surface modification in various micro-fluidic applications.}}, author = {{Marie, Rodolphe and Beech, Jason and Voeroes, Janos and Tegenfeldt, Jonas and Höök, Fredrik}}, issn = {{0743-7463}}, language = {{eng}}, number = {{24}}, pages = {{10103--10108}}, publisher = {{The American Chemical Society (ACS)}}, series = {{Langmuir}}, title = {{Use of PLL-g-PEG in micro-fluidic devices for localizing selective and specific protein binding}}, url = {{http://dx.doi.org/10.1021/la060198m}}, doi = {{10.1021/la060198m}}, volume = {{22}}, year = {{2006}}, }