Efflorescent powders refer to a class of pharmaceutical powders that contain hydrates, which are substances that have water molecules incorporated into their crystal structure. When these hydrates are exposed to a low-humidity environment or are subjected to heat, they can release water molecules, a process known as efflorescence. Although efflorescent powders aren’t a specific type … Read more
Effervescent powders are pharmaceutical dosage forms that, when dissolved in water or another liquid, produce a fizzy, carbonated solution. They typically contain an active pharmaceutical ingredient (API), along with a mixture of an acid and a base, which react to generate carbon dioxide gas when in contact with water. Effervescent powders are commonly used for … Read more
Dusting powders are topical pharmaceutical powders applied to the skin or mucous membranes for various therapeutic purposes. They are usually formulated with active ingredients and inert excipients to create a finely ground, free-flowing powder. Dusting powders can be used to treat various skin conditions, reduce friction, absorb moisture, or provide a cooling sensation. Types of … Read more
Steady State Drug Levels describe equilibrium concentration reached with repeated dosing when drug input equals elimination. Definition of Steady-State Drug Levels: Steady state (Css) is reached when the rate of drug administration = rate of drug elimination. Occurs after ~4-5 half-lives of continuous dosing. Why It Matters Maintains consistent therapeutic levels Minimizes risk of toxicity … Read more
Multicompartment Models in Pharmacokinetics explain complex drug distribution and elimination across central and peripheral compartments. The body is often not homogeneous; after administration, a drug may distribute at different rates to different tissues. Multicompartment models are used to better describe drug distribution and elimination when it doesn’t fit simple one-compartment models. Definition of Multicompartment Models … Read more
Kinetics of Multiple Dosing explains drug accumulation, steady state concentration, and dosing intervals in pharmacokinetics. Kinetics of Multiple Dosing When drugs are given at regular intervals (e.g., every 8 hours), the drug accumulates in the body until a steady state is reached. Key Concepts: Accumulation: Occurs when drug is administered before previous doses are fully … Read more
Two-Compartment Open Model The two-compartment open model is a pharmacokinetic model used to describe how drugs distribute and eliminate within the body. This model divides the body into two theoretical compartments: Central Compartment Represents the blood and highly perfused organs (e.g., heart, liver, kidneys). Site of drug administration and elimination. Peripheral Compartment Represents less perfused … Read more
Two Compartment Open Model IV Bolus describes rapid drug distribution into central and peripheral compartments with elimination kinetics. Drug is administered rapidly into the central compartment. Distribution occurs between central and peripheral compartments. Elimination happens only from the central compartment. This model describes the pharmacokinetics of a drug administered intravenously in a single dose, where … Read more
Pharmaceutical powders can be categorized as either simple or compound powders. The differences between them are outlined in the table below: Feature Simple Powder Compound Powder Composition Contains a single active pharmaceutical ingredient (API). Contains two or more active pharmaceutical ingredients (APIs) in a specific ratio. Therapeutic Effect Exerts a single therapeutic effect due to … Read more
Mixing powders is a critical process in preparing pharmaceutical products like tablets, capsules, and bulk powders. The goal is to create a homogenous blend of active ingredients and excipients for consistent dosing. Powder mixing can be done through manual or mechanical 1. Manual Mixing Manual mixing uses simple tools like spatulas, mortars, and pestles to … Read more