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Interest in microbial surfactants has been steadily increasing in recent years due to their diversity, environmentally friendly nature, possibility of large-scale production, selectivity, performance under extreme conditions, and potential applications in environmental protection.[16][17] A few of the popular examples of microbial biosurfactants includes Emulsan produced by Acinetobacter calcoaceticus,[18] Sophorolipids produced by several yeasts belonging to candida and the starmerella clade,[19][20] and Rhamnolipid produced by Pseudomonas aeruginosa[21] etc. Classification of surfactants[edit]. National Institutes of Health (NIH). M (1995). Chemosphere. The structure of surfactant layers can be studied by ellipsometry or X-Ray reflectivity. Examples of application of wetting to pharmacy and medicine include the displacement of air from the surface of sulfur, charcoal, and other powders for the purpose of dispersing these drugs in liquid vehicles; the displacement of air from the matrix of cotton pads and bandages so that medicinal solutions can be absorbed for application to various body areas; the displacement of dirt and debris by the use of detergents in the washing of wounds; and the application of medicinal lotions and sprays to surface of skin and mucous membranes.[citation needed]. Interfacial and surface tension can be characterized by classical methods such as the -pendant or spinning drop method.

Many important surfactants include a polyether chain terminating in a highly polar anionic group. Surfactant molecules have either one tail or two; those with two tails are said to be double-chained. "Production of biosurfactants by Cladosporium resinae". and Marhaendrajana, T. Environmental pollution (Barking, Essex: 1987). You can help by converting this section to prose, if appropriate. The head of an ionic surfactant carries a net positive, or negative charge.

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