Tissue sterilization

Fridman, G., et ah Blood coagulation and living tissue sterilization by floating-electrode dielectric barrier discharge in air. Plasma Chemistry and Plasma Processing 26(4), 425 42 (2006)... 

Processing in Hquid sterilants results in wet products which require highly specialized packaging. Therefore, Hquid sterilization should only be considered if the sterilized article is to be used almost immediately. Liquid sterilants or their residues can be harmful to living tissues. Therefore it is always necessary to rinse articles with sterile water or saline solution foUowing treatment. Whereas Hquid sterilization is an extremely useful method for articles that caimot withstand the conditions of steam sterilization, the problems associated with its use limit its appHcation. 

Each interferon preparation was ultracentrifuged at 20,000 revolutions per minute for one hour to remove tissue debris and inactivated virus. The supernatant was dialyzed against distilled water (1 400) for 24 hours at4°C. The material was then freeze-dried. The dried product was reconstituted in one-tenth of the original volume in distilled water and dispensed into ampoules. Reconstituted solutions were assayed for interferon activity, examined for toxicity, and tested for sterility. 

Other applications of filters include sterilization of venting or displacement air in tissue and microbiological culture (carbon filters and hydrophobic membrane filters) decontamination of air in mechanical ventilators (glass fibre filters) treatment of exhausted air ftom microbiological safety cabinets (HEPA filters) and the clarification and sterilization of medical gases (glass wool depth filters and hydrophobic membrane filters). 

The reduction of blood loss during or after surgical procedures where suturing or hgature is either impractical or impossible can often be accomphshed by the use of sterile, absorbable haemostats. These consist of a soft pad of sohd material packed around and over the wound which can be left in situ, being absorbed by body tissues over a period of time, usually up to 6 weeks. The principal mechanism of action of these is the ability to encourage platelet fiacture because of their fibrous or rough surfaces, and to act as a... 

This is composed of the sodium and ealeium salts of alginic add formed into a powder or fibrous material and sterilized by autoelaving. It aids clotting by forming a sodium-caldum alginate complex in contact with tissue fluids, acting principally as a mechanical haemostat. It is relatively slowly absorbed and some residues may occasionally remain in the tissues. 

In some cases pectinolytic enzymes have been associated with virulence and it is generally accepted that pectinolysis by these bacteria facilitates their entry and spread in plant tissue. In Rhizohium, these enzymes may play a role in the root infection process that precedes nodule formation (Hubbell et al 1978). A. irakense has never been reported to be pathogenic on plants. It can therefore be speculated that moderate and strictly regulated pectinolysis of A. irakense facilitates entry in the outer cortex of plants roots, since A. irakense has been isolated from surface-sterilized roots. It is likely that breakdown of plant polysaccharides by root colonizing bacteria can provide them with extra carbon source. 

Infection Inflammatory response to invasion of normally sterile host tissue by microorganisms. 

Two studies have used single cells to study the effect of phenolic acids on mineral absorption. In sterile cell cultures of Paul s Scarlet rose, 100 pM ferulic acid inhibited Rb+ absorption in about 10 min when the cells were 4-5 days old (37). Uptake from 0.2 mM RbCl was inhibited about 25% and absorption from 5.0 mM RbCl was inhibited 45%. Absorption by 10-day-old cells was affected little. Salicylic acid at 10 pM inhibited PO - absorption by Scenedesmus, a unicellular green alga (38). These studies show that allelochemicals inhibit mineral absorption in cellular systems as well as tissue systems (Table I). 

---