Skip to content

Latest commit

Β 

History

History
63 lines (41 loc) Β· 3.31 KB

File metadata and controls

63 lines (41 loc) Β· 3.31 KB

Routes & Formulations

The absorption, distribution, and overall effect of a drug in the body depend on both the route of administration and the formulation used. Drugs are delivered in specific units called dosage forms, each tailored to optimize efficacy, stability, and patient compliance.

πŸ’Š Dosage Forms

A dosage form refers to the physical form of a drug product suitable for administration. A single drug may be available in multiple dosage forms, each designed to modify how the drug is delivered and absorbed. Selection depends on patient needs, target effect location, and pharmacokinetics.

πŸ”‘ Local vs Systemic Effects

  • Local Effect: Drug activity is limited to the site of application (e.g., topical cream).
  • Systemic Effect: Drug enters systemic circulation and acts at distant sites (e.g., oral tablet, IV injection).

πŸ§ͺ Composition of Dosage Forms

Dosage forms consist of:

  • Active Ingredient: The pharmacologically active compound.
  • Inactive Ingredients (Excipients): Substances included to aid manufacturing, stability, delivery, or absorption.
Excipient Type Purpose Common Dosage Forms
Binders Hold ingredients together in a cohesive unit Tablets
Lubricants Prevent sticking to manufacturing equipment Tablets, Capsules
Disintegrants Promote breakup of the dosage form after intake Tablets, Capsules
Diluents Add bulk to formulations for proper dosing Tablets, Capsules, Lyophilized Powders
Preservatives Prevent microbial growth Liquids, Ophthalmics, Topicals
Flavoring Agents Improve palatability Oral Liquids, Chewable Tablets
Colorants Aid in product identification Tablets, Capsules
Solvents Dissolve active ingredients Solutions, Injectables
Coating Agents Mask taste or control release Enteric-coated, Extended-release tabs

πŸ“Œ Note: Not all excipients are inert for all patients. Some may cause allergies or intolerances.

🧫 Solubility & Absorption

A drug's solubility is its ability to dissolve in a solvent, typically water or biological fluids. This property directly influences absorption, especially for enteral and parenteral routes.

πŸ”‘ A drug must be dissolved before it can be absorbed into the bloodstream. Poor solubility often leads to poor bioavailability.

Property Effect on Drug Performance
High Solubility Faster dissolution, quicker onset
Low Solubility Slower or incomplete absorption

πŸ“Œ Solubility can be modified using salts, particle size reduction, or formulation with solubilizing agents.

πŸ›€οΈ Routes of Administration

Routes of administration are classified into two broad categories:

πŸ“Œ Each route affects onset, bioavailability, and duration of action.


πŸ—ΊοΈπŸ”— Nav Links