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Particles that achieve a maximum zeta potential reach a point of maximum stability with respect to dispersion, thermodynamically 18 Nash 44 If in di ion the viscosit of the vehicle can be increased sufficient! As has been noted, these two conditions are difficult to achieve for many insoluble drugs.
Many pharmaceutical suspensions are not capable of achieving a state of complete electrostatic repulsion and thus the method of producing a colloidally stable suspension has been thought to be unworkable by many The a lication of zeta otential in accordance wi h 0 ri i inv s i ors Landau, Verwey, and Overbeek's theory, which governs the preparation of colloidally s a e suspensions, as een ex ensive y reviewe y c nei er ea. Flocculated Suspensions Haines and Martin , Hiestand , and Ecanow and coworkers  are generally credited with establishing the "structured particle" concept or flocculated pharmaceutical suspension.
The following definitions should prove useful in avoiding confusion among three closely related terms: In agglomeration, a large number or mass of particles are closely bound together refers to the massing of particles in a liquid state alone and sometimes in the form of a U1 ge structure.
The particles of such coagulated systems are held together by strong film-film bonds. Coagulated suspensions, like colloid dispersion and unlike flocculated suspension, tend to "cake" on standing. Soon after milling and suspension, unless steps are taken to prevent it, microme. This phenomenon tends to promote "caking or cementing" together of particles.
The creation of a protective coat or boundary layer with a hydrophilic colloid about such particles offers the best protection to crystal growth. Since protective barriers may or rna not flocculate the substrate articles the si n ositive or ne ative and the ch r potential on the particle surface will govern the choice between flocculation or disper. Accordin to Fi.
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