Antimicrobial adhesion

Alcloxa Phytosphingosine antimicrobial, adhesives Bispyrithione 2-Bromo-2-nitropropane-1,3-diol p-Chloro-m-cresol Copper pyrithione Quaternium-15... 

Textile Finishing. Polyethyleneimine-A/-methylolurea derivatives improve the crease and wear resistance of cotton (429,430). The adhesion between individual wool fibers is improved by pretreatment with amines, which leads to improved shrink resistance (431). An antimicrobial finish can be appHed to cotton by using a combination of PEI and ureas to bind zinc pyrithione to the fabric (432). After wool has been provided with a flameproof finish using fluorozirconate or fluorotitanate, the wool can be neutralized with PEI (433). Conventional neutralizing agents caimot be used for this purpose since they impair the flameproof characteristics of the impregnated fabric. 

Another compound, the antimicrobial action of which is associated with chelation, is 2-pyridinethiol-A/-oxide [3811-73-2] (Omadine). Activity has been shown to depend on coordinating property. The iron chelate is active, but not the free pyridine compound (200). In the form of its zinc chelate it is found in shampoos to control seborrheic dermatitis (201). Other appHcations of this useful chemical include preservation of adhesives, plastics, latex paints, polyurethane foam, and metal working fluids (202). 

The introduction of retro-, retro-inverso-, and PMRI-peptides with free and blocked C-and N-termini has been successful in numerous biological systems such as neurotransmitters, inhibitors of proteases and protein kinases, sweeteners, antimicrobial peptides, hormones, adhesion molecules, antigenic epitopes, immuno-modulators, and immunological probes. Table 1 provides an exhaustive list of retro-, retro-inverso-, PMRI-, and end-group-modified re/ro-mvmo-pseudopeptides derived from bioactive peptides. 

The activities of the purple fluid of the sea hare Aplysia dactylomela, such as toxic, antimicrobial and hemagglutinating properties, have been attributed to a substance of protein nature [332], Proteoglycans and adhesive glycoproteins present in the extracellular matrix of vertebrates, have also been reported in sponges. These molecules are probably involved in the cell adhesion systems of sponges [333], Recently, novel marine proteins have been reported, such as silicatein from sponge biosilica [334], and a metallothionein protein from the marine alga Fuats vesiculosus [335], Metallothioneins have also been isolated from Arctic... 

IFN-y also induces the costimulatory molecules on the macrophages, which increases cell-mediated immunity. As a consequence, there is activation and increase in the tumoricidal and antimicrobial activity of mononuclear phagocytes, granulocytes and NK cells. The activation of neutrophils by IFN-y includes an increase in their respiratory burst. IFN-y stimulates the cytolytic activity of NK cells. It is an activator of vascular endothelial cells, promoting CD4+ T lymphocyte adhesion and morphological alterations, which facilitates lymphocyte extravasation. IFN-y promotes opsonization by stimulating the production of IgG subclasses that activate the complement pathway. A summary of the characteristics of selected cytokines is shown in Table 2.3. 

Many microbial infections and toxins are spread by biofilms. Biofilm formation occurs on virtually every surface, starting with the adhesion of planctonic cells or small dispersed biofilm fragments. Proliferation of the cells is accompanied by the expression of an extracellular polysaccharide-based matrix [6], The cells embedded in this matrix are well protected and up to 1000 times less susceptible to antibiotics [7], Once a biofilm is formed, it is extremely difficult to remove this contamination. Thus, all antimicrobial surfaces should prevent the primary attack [8], One class of antimicrobial surfaces prevents the primary attack by creating surfaces that are not sticky to microbial cells, i.e., they do not allow adhesion of these cells. The other major class of antimicrobial surfaces is based on the killing of approaching microbes (see Fig. 2). Interestingly, both approaches can be achieved either by permanent surface modifications or by releasing bioactive compounds. 

Fig. 9 Example of a contact-killing and microbe-repelling surface, (a) Antimicrobial cationic polyW.iV-dimethyl-iVTethoxycarbonylmethyll-iV-P -tniethacryloyloxylethyll-ammonium bromide) left structure) effectively kills bacteria, (b) The polymer is converted into the corresponding nonfouling zwitterionic derivative (right structure) upon hydrolysis, (c) Dead bacteria remaining on the surface are repelled from the nonfouling surface, (d) The zwitterionic surface itself is highly resistant to bacterial adhesion. Reproduced and adapted from [136]...

Lipopolysaccharides are heat-stable complex amphiphilic macromolecules indispensable for the bacterial growth, viability and for the correct assembly of the external membrane they represent a defensive barrier which helps bacteria to resist to antimicrobial compounds and environmental stresses and are involved in many aspects of host-bacterium interactions as recognition, adhesion, colonization, and, in the case of extremophile bacteria, in the survival under harsh conditions (Alexander and Rietschel, 2001 Raetz and Whitfield, 2002 Raetz et al 2007). LPS are also called endotoxins because they are cell-bound and, once released, play a key role in the pathogenesis of Gram-negative infections, in mechanisms as... 

Mediates leukocyte adhesion and activation, allowing them to bind to the endothelium and migrate across it. In neutrophils, a potent chemoattractant and able to induce the formation of reactive oxygen species and the release of lysosomal enzymes by these cells. Potent vasodilator, relaxes smooth muscle, reduces platelet aggregation, aids in leukocyte recruitment, has direct antimicrobial activity in high concentrations. A group of lipids which can cause vasodilation, fever and pain. 

---