Adjuvant types

Sharma, S.D. and M. Singh (1999). Effect of two adjuvant types on the distribution of 14C-glyphosate applied to model weed species. 

When an adjuvant type test method for skin sensitization is used, a response of at least 30% of the animals is considered as positive. For a non-adjuvant test method a response of at least 15% of the animals is considered positive. Test methods for skin sensitization are described in the OECD Guideline 406... 

Green, J. M., and Hale, T., Effect of Adjuvant Type on the Control of Yellow Foxtail (Setaria Glauca) with Nicosulfuron, Proceedings Weed Science Society of America, 43 58,2003. 

Formulation. Compressed tablet formulations contain several types of inert, adjuvant ingredients necessary for proper preparation and therapeutic performance. Tablets designed to be swallowed need diluent, disintegrating, binding (adhesive), and lubricating inert ingredients, whereas... 

The main purpose of pesticide formulation is to manufacture a product that has optimum biological efficiency, is convenient to use, and minimizes environmental impacts. The active ingredients are mixed with solvents, adjuvants (boosters), and fillers as necessary to achieve the desired formulation. The types of formulations include wettable powders, soluble concentrates, emulsion concentrates, oil-in-water emulsions, suspension concentrates, suspoemulsions, water-dispersible granules, dry granules, and controlled release, in which the active ingredient is released into the environment from a polymeric carrier, binder, absorbent, or encapsulant at a slow and effective rate. The formulation steps may generate air emissions, liquid effluents, and solid wastes. 

Compared to wild-type mice, in TRPVl gene-deleted (—/—) mice, complete Freund s adjuvant evokes significantly less oedema, hyperalgesia and arthritis score [149]. 

The selection of vehicle is based on the type of lesion and location of the infection. Solutions are recommended for hairy areas and oozing lesions, while creams are better for moderately scaling and non-oozing lesions. For hyperkeratotic lesions, ointments can be considered. The selected formulation should be applied to the affected area after it is cleaned and dried. The medication should be rubbed into the infected area for improved penetration. Since most patients do not rub in sprays and powders, penetration of the epidermis is minimal, making them less effective than other formulations. Sprays and powders should be considered as adjuvant therapy with a cream or lotion or as prophylactic therapy to prevent recurrence. 

AIA, adjuvant-induced arthritis CFA, complete Freund s adjuvant CIA, collagen-induced arthritis DTH, delayed-type hypersensitivity LPS, lipopolysaccharide. 

In addition, LS have several advantages over other delivery systems good physical stability, low cost of ingredients, ease of preparation and scale-up, and high entrapment yields for hydrophobic drugs. Moreover, LS have been successfully used both for the controlled delivery of various types of drugs and as carriers of vaccines and adjuvants [29,31,32]. 

Olbrich, C. and Muller, R.H., Tabatt, K., Kaiser, O., Schulze, C., and Schade, R., Stable biocompatible adjuvants — a new type of adjuvant based on solid lipid nanoparticles a study on cytotoxicity, compatibility and efficacy in chicken, Alternatives to Laboratory Animals, 2002, 30, 443 158. 

One particularly novel carrier was reported to consist of 50-70 nm colloidal gold particles of the type often used in cytochemical labeling techniques for microscopy (Pow and Crook, 1993) (Chapter 24). Adsorption of peptide antigens onto gold and subsequent injection of the complex into rabbits in an adjuvant mixture resulted in rapid production of antibody of extremely high titer. The resultant antibodies could be used in immunocytochemistry at dilutions from l-in-250,000 down to l-in-1,000,000, which is orders-of-magnitude beyond the dilutions typically used with lower-titer antibodies. 

Porosity calculations from density measurements have also been applied to granulations prepared using different processes. The method of granulation, such as the type of adjuvant used [64] or the amount of granulation liquid [74], was found to change the bulk density and porosity of the material. Consequently, the compression and flow properties of the materials were also different. 

The structure of the native immunostimulatory MDPs was found to be IV-acetyl muramyl-L-alanyl-D-isoglutamine. (/V-Acetyl muramic acid is a base component of bacterial peptidoglycan.) Native TDM is a potent pyrogen and is too toxic for general use as an adjuvant. The molecular basis underlining MDP s adjuvanticity remains to be fully elucidated. Administration of MDP, however, is known to activate a number of cell types that play direct/indirect roles in immune function, and induces the secretion of various immunomodulatory cytokines (Table 13.14). 

A variety of lipid adjuvants and protein mediators have also been shown to influence the immune response to antigens encapsulated in liposomes. The most widely used examples of such adjuvants for practical immunization procedures are endotoxin (including lipid A and lipopolysaccharide) and numerous types of lipophilic derivatives of muramyl dipeptide. 

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