Page 405 - Academic Press Encyclopedia of Physical Science and Technology 3rd Chemical Engineering
P. 405

P1: GLQ Final Pages
 Encyclopedia of Physical Science and Technology  EN009K-419  July 19, 2001  20:57






               340                                                                         Membranes, Synthetic, Applications






























                FIGURE 51 Schematic of artificial pancreas under development based on a membrane unit (Circe Biomedical, Inc., Lexington, MA).


               certain minimum level to obtain the desired therapeutic  is controlled by the size of the patch. The patch may be
               effect, but below the point where toxic side effects occur.  removed to discontinue drug delivery instantly. Devices
               Once the desired level is reached, it should be maintained  of this type have been used to administer nitroglycerine
               over an extended period without further intervention from  for treating angina.
               the user. Controlled release technology based on the use of  Still another dosage form is microcapsules, which are
               synthetic membranes is an effective approach to address-  tiny droplets of an active agent coated with a permselective
               ing these issues.                                 barrier polymer, all in the form of a suspension. Micro-
                                                                 capsules are conveniently formulated for injection. In such
                                                                 cases the barrier polymer is often chosen to be degradable
                 1. Passive Controlled Release                   into innocuous products in the body after the active agent
               In one type of controlled-release device, an active agent is  has been dispensed.
                                                                   Osmotic pumps operate by a different principle. In
               dissolved at its solubility limit in a reservoir surrounded
                                                                 one design, the active agent is mixed with an osmotic
               by a membrane. By providing excess agent in the reser-
                                                                 agent such as salt or sucrose, and covered with a water-
               voir (e.g., by physical mixing or compounding), a constant
                                                                 permeable membrane. When the device is immersed in
               permeation driving force is exerted on the membrane. In
                                                                 water and the infusion of water generates a pressure
               this way a constant release rate is achieved until the agent
                                                                 inside the membrane, the active agent is forced out of
               concentration drops below saturation. Release rate is de-
                                                                 the device through metering holes or capillaries on the
               termined by the solubility and diffusivity of the agent in
                                                                 surface of the membrane. Alternatively, the active agent is
               the membrane. Tailoring the chemistry and geometry of
                                                                 packaged within a sac that separates it from the osmotic
               the device provides different release profiles and capac-
                                                                 agent, which in turn is confined by the water-permeable
               ities. Devices of this type have been developed for ad-
                                                                 membrane. The pressure generated by the wetted osmotic
               ministering steroids for fertility control or hormone ther-
                                                                 agent compresses the sac and exudes the active agent from
               apy, or intraocular dispensing of pilocarpine for glaucoma
                                                                 the device.
               control. For nonmedical applications, similar devices are
               available in multilayer laminate form for dispensing insect
                                                                   2. Active Controlled Release
               pheromones, insecticides, fragrances, and bactericides.
                 Sometimes the human skin is used as the rate-   A novel approach to controlled release integrates biosens-
               controlling membrane for certain pharmaceuticals that  ing and control functions in a single membrane device.
               are readily absorbed. A removable skin patch containing  As an example, a membrane responds to changes in glu-
               the drug is applied directly on the body to provide a  cose level in the body by automatically changing its per-
               reservoir of specific capacity; the rate of administration  meability to insulin. The response mechanism is shown
   400   401   402   403   404   405   406   407   408   409   410