Mixed SAMs

Structural types Homopolymers Copolymers (alternating, block, and random) Linear, branched, cross-linked, dendrimeric, etc. Homogeneous SAMs Mixed SAMs Patterned SAMs... 

Consider now an encounter (F) radical pair formed from two free radicals. Since there are three components to the triplet state, T+i, To and T j, and only one singlet component, S, the encounter of two free radicals having uncorrelated spins leads to a statistical distribution of T and S radical pairs. However, some of the S radical pairs will react without undergoing T-S mixing, and this has the effect of increasing the relative number of T radical pairs. Consequently the F-pairs will give the sam e type of polarization as the T-pairs, but the degree of polarization will be less. 

Fig. 3 Relationship between water contact angles on mixed SAMs and the number of adherent cells. HUVECs (open circles) and HeLa cells (filled circles) were allowed to adhere for 1 h. The averages ( SEM) of five experiments are shown [21]...

We examined protein adsorption to SAMs that carried four different functional groups [42] and mixed SAMs with different wettabilities [21], Large amounts of serum proteins adsorbed to all these SAMs, but the different surface functional groups greatly affected cell adhesion behavior (Figs. 2 and 3). Thus, the amount of adsorbed proteins did not correlate with the degree of cell adhesion to SAMs. 

We investigated the efficiency of NSC expansion on surfaces with EGF-His immobilized in the correct orientation. NSCs were obtained from neurosphere cultures prepared from fetal rat striatum harvested on embryonic day 16. NSCs were cultured for 5 days on EGF-His-immobilized substrates prepared with mixed SAMs of different COOH-thiol contents. Cells adhered and formed network structures at a density that increased with the COOH-thiol content of the surface. As a control, cells were seeded onto surfaces without immobilized EGF-His. This resulted in poor cell adhesion during the entire culture period. In addition, when EGF-His adsorbed to SAMs with 100% COOH-thiol or SAMs with NTA-derivatized COOH that lacked Ni2+ chelation, we observed poor initial cell adhesion, and the cells formed aggregates within 5 days. Interestingly, the substrate used to covalently immobilize EGF-His with the standard carbodiimide chemistry was not a suitable surface for cell adhesion and proliferation. The control experimental results contrasted markedly with results from EGF-His-chelated surfaces. 

Reproduced from Nakaji-Hirabayashi et al. [85] with permission from Elsevier, copyright 2007 Content in the solution used to prepare the mixed SAMs bDetermined with a microBCA assay Mean standard deviation for n = 5 assays... 

We also conducted experiments to compare our culture method with the standard neurosphere culture. In the standard neurosphere culture, cell number increased approximately nine times over 5 days. Immunostaining showed that the neurosphere cultures contained 54 5.3% nestin+ cells and 41 7.4% nestin+ pIIF cells. This demonstrated that the standard neurosphere culmring method was less efficient than EGF-immobilized substrates for selectively expanding NSCs. Thus, the EGF-immobilized substrates prepared from mixed SAMs with 10% COOH-thiol provided the most efficient method for selective NSC expansion. 

Based on those results, we concluded that, when cultured on the EGF-His-immobilized surface prepared from a mixed SAM of 10% COOH-thiol, highly enriched NSC populations could be produced in large quantities. Over a 5-day culture on the substrate, cells were expanded 32 times. These expanded cells consisted of 98% nestin+ cells that retained multipotency for differentiation into neuronal and glial lineages. This suggested that selective expansion could be repeated for large-scale production of highly enriched NSC cells. 

B. Ge and F. Lisdat, Superoxide sensor based on cytochrome c immobilized on mixed-thiol SAM with a new calibration method. Anal. Chim. Acta. 454, 53-64 (2002). 

The high surface coverage and near-crystalline structure of SAMs has limited their application as stationary phases in RPLC. Wirth et al. [70,71] have described the preparation of SAM-based chromatographic materials with the use of mixed... 

In a scheme complementary to the one just presented where thiols are removed by reductive desorption of thiols, molecules can also be removed during stripping of a UPD layer. This was demonstrated by Shimazu et al. [221] where an alkane thiol SAM was deposited onto a Au(l 11) that had been modified with Pb. Oxidative stripping of the lead also caused thiols to be removed. The empty sites were then subsequently filled with mercaptopropionic acid (MPA). A remarkable result is that the binary SAMs exhibit only one desorption peak. From this it was concluded that a well-mixed layer forms that is very different from the mixed SAM obtained by adsorption from solution containing both types of thiols. In this case the layer exhibits singlecomponent domains that are refiected by two desorption peaks. 

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