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Procedure for Standard Surface Modification using the Aldrich® Kit for Creating Hydrophilic PDMS Surfaces

Product Description

Use of this kit results in a durable hydrophilic PDMS surface. The resulting surface should be wettable by hydrophilic inks and appropriate for multiple printing applications. After treatment, water should completely wet the surface as the water contact angle is expected to be between 25 and 35 °.

Components

Solution A - 10 mL
(Glycidyl methacrylate based polymer)
Solution B - 4 mL
(Acrylamide/acrylic acid based polymer)

Solvents recommended, but not provided

  1. Ethanol (Catalog Number 245119)
  2. 2-Butanone (Catalog Number 230294)
  3. Water (Catalog Number 320072)

Precautions and Disclaimer

This product is for R&D use only, not for drug, household, or other uses. Please consult the Safety Data Sheet for information regarding hazards and safe handling practices.

Storage/Stability

Store the kit at room temperature.

Procedure

Procedure for standard surface modification

Procedure for standard surface modification
  1. Pretreatment - PDMS surface should be activated using a low frequency air plasma treatment for 1 minute (Recommended plasma cleaners: Catalog Numbers Z561673, Z561681, Z561657, and Z561665).
  2. Prerinsing - The plasma activated PDMS sample should be rinsed by washing with ethanol (Catalog Number 245119) for at least 10 minutes. The rinsing procedure should be repeated 3 times. Then, the sample should be air-dried for at least 15 minutes. The water contact angle of the resulting activated PDMS surface is expected to be between 25 and 40 °C.
  3. First Modification Step - The surface of the horizontally positioned sample prepared in the previous step should be covered with Solution A, typically ~1 mL per square inch of the surface. The sample should be dried under ambient conditions for 20–30 minutes and annealed at 110 °C under nitrogen or argon for 30 minutes.
  4. Rinsing - The annealed sample should be rinsed three times with 2-Butanone (Catalog Number 230294) for 10 minutes each time. Then it should be air-dried for at least 30 minutes.
  5. Polymer Grafting - 6 mL of ethanol must be added to the container containing Solution B. Stir the mixture to homogeneity. The surface of the horizontally positioned sample prepared previously should be treated by completely covering the area to be modified with the homogeneous solution, typically ~1 mL per square inch of the surface. The sample should be dried under ambient conditions for 20–30 minutes, then annealed at 80 °C for 14 hours. Finally, the unattached polymer should be removed from the sample by a thorough rinse with water (Catalog Number 320072) and the sample air-dried at room temperature.
Materials
Product No.Product NameDescriptionPricing
SCM122AdipoMAX Differentiation Medium
TMS-010Alcian-Blue Staining Solution
TMS-008Alizarin-Red Staining SolutionAlizarin red is a commonly used stain to identify calcium containing osteocytes in differentiated culture of both human and rodent mesenchymal stem cells (MSCs).
CBL154Anti-H-CAM Antibody, clone F10-44-2clone F10-44-2, Chemicon®, from mouse
MAB4315Anti-STRO-1 Antibody, clone STRO-1ascites fluid, clone STRO-1, Chemicon®
CBL415Anti-Thy-1 Antibody, clone F15-42-1clone F15-42-1, Chemicon®, from mouse
SCM123ChondroMAX Differentiation Medium
CLS431751Corning® cell strainerpore size 70 μm, white, sterile, pkg of (individually wrapped), pack of 50 ea, Corning 431751
D2650Dimethyl sulfoxideHybri-Max, sterile-filtered, BioReagent, suitable for hybridoma, ≥99.7%
ES-020-BFetal Bovine SerumUS Origin, Mesenchymal Stem Cell Qualified FBS, sterile-filtered, suitable for stem cell culture
F0291hBFGFFGF-Basic, recombinant, expressed in E. coli, suitable for cell culture
SCC038Human Adipose Mesenchymal Stem CellsHuman Adipose Mesenchymal Stem Cells (MSCs) are isolated from human adipose tissue and are cryopreserved at P2 to ensure optimal phenotype and the highest viability and plating efficiency.
SCC034Human Mesenchymal Stem Cells (Bone Marrow)Human mesenchymal stem cells derived from bone marrow that have a capacity for expansion in vitro while maintaining their potential for differentiation to multiple lineages including adipocytes, osteoblasts and chondrocytes.
C-12971Human Mesenchymal Stem Cells (hMSC)Derived from umbilical cord matrix, 500,000 cryopreserved cells
C-12974Human Mesenchymal Stem Cells (hMSC)Derived from bone marrow, 500,000 cryopreserved cells
C-12975Human Mesenchymal Stem Cells (hMSC)Derived from bone marrow, 500,000 proliferating cells
C-12977Human Mesenchymal Stem Cells (hMSC)Derived from adipose tissue, 500,000 cryopreserved cells
C-12972Human Mesenchymal Stem Cells (hMSC)Derived from umbilical cord matrix, 500,000 proliferating cells
C-12978Human Mesenchymal Stem Cells (hMSC)Derived from adipose tissue, 500,000 proliferating cells
C-14090Human Mesenchymal Stem Cells (hMSC)Derived from bone marrow, 1 million cells per pellet
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