By Anya M Hillery, Kinam Park
This e-book offers a complete creation to complex drug supply and focusing on, overlaying their rules, present functions, and power destiny advancements. This variation has been up to date to mirror major traits and state of the art advances that experience happened because the first version used to be released. the entire unique chapters were retained, however the fabric therein has been up to date. 8 new chapters were additional that care for completely new applied sciences and approaches.
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Additional resources for Drug Delivery: Fundamentals and Applications
1968. GBH coatings on plastics and metals. Ann NY Acad Sci 146:21–29. Harada, A. and K. Kataoka. 1995. Formation of polyion complex micelles in an aqueous milieu from a pair of oppositely charged block copolymers with poly(ethylene glycol) segments. Macromolecules 28:5294–5299. S. 2008. The origins and evolution of “controlled” drug delivery systems. J Control Release 132:153–163. , G. Schmer, C. Harris et al. 1972. Covalent binding of biomolecules to radiation-grafted hydrogels on inert polymer surfaces.
Chemical approaches utilize chemical degradation, or enzymatic degradation, to effect CR of drug molecules from a drug–polymer conjugate. 1 Dissolution Control The drug is associated with a polymeric carrier, which slowly dissolves, thereby liberating the drug. The polymeric carrier can be as follows: 1. A reservoir system (encapsulated dissolution system), whereby a drug core is surrounded by a polymeric membrane. The rate of drug release is determined by the thickness and dissolution rate of the membrane.
Controlled release (CR): In this type of drug release, the drug is released at a predetermined rate for a prolonged period of time, so that effective drug plasma levels are maintained and controlled over an extended period of time. In contrast to SR dosage forms, CR delivery systems aim to control both the drug release from the dosage form and also the subsequent plasma levels; therefore, in principle at least, plasma levels are solely determined by the drug release kinetics from the DDS. The plasma profile from a CR DDS would then be similar to that achieved via an intravenous infusion.
Drug Delivery: Fundamentals and Applications by Anya M Hillery, Kinam Park