Tecnotest Reflex 3130 Serial

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NewMediaAlliance is a free community focused on mobilizing a global network of users and activists to reform and democratize society by broadening access to quality public media.The present invention relates to the manufacture of a solid dosage form for a pharmaceutical active agent.
The term “solid”, as used herein, refers to any material which can be handled and retained in the hands, but is not in true solution form. Such materials include, but are not limited to, powders and granules. The present process may be used to manufacture a variety of solid dosage forms, such as, powders, pellets, tablets, lozenges, pills, capsules, beads, and caplets, and more specifically to manufacture a solid oral dosage form having a layer of a pharmaceutical active agent.
It is well known that several factors influence the preparation of solid oral dosage forms for a pharmaceutical active agent. These factors include the amount of the active agent and the active agent’s solubility in the preparation medium. The active agent must be dissolved in the preparation medium to be released from the dosage form. Tablets and capsules have been a popular dosage form for some active agents. Other popular dosage forms have included powders, pellets, and lozenges. The manufacture of tablets and capsules involves incorporating the active agent into a preparation medium. Powders, pellets, and lozenges are prepared by compression or encapsulation, which generally requires the active agent to be dissolved or suspended in the preparation medium. Recently, solid oral dosage forms have been developed that utilize a mucosal membrane, such as, the buccal mucosa, to deliver the active agent. In these forms, a hydrophobic matrix is prepared in which the active agent is incorporated. The matrix is designed to dissolve slowly and release the active agent.
A number of processes have been developed to prepare solid oral dosage forms.
U.S. Pat. No. 5,429,838 discloses a method for producing a solid dosage form for an active agent having a controlled rate of release. The active agent is incorporated into an enteric matrix. The enteric matrix is prepared by admixing a polymeric acid with an enteric polymer having carboxylic acid groups. An example of
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