Industrial Pharmacy I

Formulation and Manufacture of Aerosols

  • Formulation and Manufacture of Aerosols involve selecting suitable propellants, solvents, and active ingredients for stability and delivery.
  • Formulation and Manufacture of Aerosols also include filling, sealing, and quality control for efficient drug release.
  • The formulation of aerosols requires careful selection and combination of ingredients to achieve desired performance.

Formulation Components:

  • Active Pharmaceutical Ingredient (API): Must be stable and uniformly dispersed or dissolved.
  • Propellant: As discussed, it drives the delivery mechanism and must be chosen based on its compatibility.
  • Co-solvents: Sometimes used to aid solubility or improve spray characteristics (e.g., ethanol).
  • Surfactants/Dispersants: Ensure proper dispersion in suspension aerosols and prevent aggregation.
  • Stabilizers and Antioxidants: Prevent degradation of sensitive APIs or excipients.

Manufacturing Process:

  1. Batch Preparation: The API is combined with excipients under controlled conditions. For solutions, complete dissolution is necessary; for suspensions, uniform dispersion is critical.
  2. Filling Process: The formulation is filled into pre-sterilized, pressurized containers using automated, high-precision filling lines designed to prevent air inclusion and contamination.
  3. Addition of Propellant: The propellant is either introduced in bulk under pressure (in canister-based systems) or loaded separately in dual-chamber systems.
  4. Crimping/Sealing: A valve is affixed to the container, and the system is sealed to maintain internal pressure and sterility.
  5. Quality Assurance: In-process controls and final product testing (such as weight, fill volume, and dose uniformity) are essential.

Process Considerations for Formulation and Manufacture of Aerosols:

  • Aseptic Processing: In many cases, especially for parenteral formulations, an aseptic environment is required.
  • Environmental Controls: Temperature, humidity, and particulate matter must be controlled during manufacturing.
  • Automation and Validation: The use of automated filling and sealing ensures uniformity and reproducibility.

Thank you for reading from Firsthope's notes, don't forget to check YouTube videos!

FirstHope

Recent Posts

Absorption of Drugs

Absorption of Drugs refers to the process by which a drug enters the bloodstream from…

9 hours ago

Allergy (Drug Hypersensitivity)

Allergy (Drug Hypersensitivity) is an abnormal immune reaction to a drug, causing effects like rash,…

9 hours ago

Distribution of Drugs

Distribution is the reversible transfer of a drug from the bloodstream to various tissues and…

9 hours ago

Metabolism (Biotransformation) of Drugs

Metabolism of drugs involves enzymatic conversion into active or inactive metabolites for easier elimination. Definition…

9 hours ago

Enzyme Induction and Inhibition

Enzyme induction and inhibition alter drug metabolism, affecting drug activity, duration, and interactions. Enzyme Induction:…

9 hours ago

Excretion of Drugs

Excretion of drugs is the process of eliminating drugs and metabolites mainly via kidneys, bile,…

9 hours ago

This website uses cookies.