Pharmacokinetics Models, Dosing & Parameters Notes [U-3]
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Pharmacokinetics
- Pharmacokinetics: Definition and Introduction
- Plasma Drug Concentration-Time Profile
- Reaction Kinetics: Rate, Rate Constants, and Order
- Compartmental Models in Pharmacokinetics
- Non-Compartment Models (Model-Independent Approach)
- Physiological Models (PBPK – Physiologically Based Pharmacokinetic Models)
- One-Compartment Open Model
- One-Compartment Model with Intravenous Bolus Administration
- One-Compartment Model with Intravenous Infusion
- One-Compartment Model with Extravascular Administration
Pharmacokinetics parameters
- Pharmacokinetic Parameters
- Methods of Drug Elimination
Other Units of Biopharmaceutics and Pharmacokinetics
Biopharmaceutics and Pharmacokinetics
Other Subjects of B Pharmacy 6th Semester
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- Anti-TB, UTI & Antiviral Agents
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- Intro to Drug Design & QSAR Approaches
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- Quality Assurance, GMP, ICH, QbD & Quality System
- GMP: Personnel, Premises & Equipment Control
- Quality Control and Good Laboratory Practice
- Complaints & Document Management
- Calibration and Warehousing
Unit-III: Pharmacokinetics Models Dosing & Parameters Notes
This unit provides an overview of pharmacokinetics, focusing on drug movement through the body using various models and key parameters.
1. Introduction to Pharmacokinetics
- Definition: The quantitative study of drug absorption, distribution, metabolism, and excretion (ADME).
- Models Used:
- Compartment Models: Simplified representations like one-compartment or multi-compartment systems.
- Non-Compartment Models: Model-independent methods based on statistical moment theory.
- Physiological Models: Based on actual anatomical and physiological parameters of organs and tissues.
2. One-Compartment Open Model
- Intravenous Injection (Bolus): Immediate input of drug into systemic circulation.
- Intravenous Infusion: Continuous drug administration at a constant rate.
- Extravascular Administration: Includes oral, intramuscular, and subcutaneous routes where absorption phase is involved.
3. Pharmacokinetic Parameters
- Kel (Elimination Rate Constant)
- CL (Clearance)
- t½ (Half-life)
- Vd (Volume of Distribution)
- AUC (Area Under the Curve)
- Ka (Absorption Rate Constant)
- Clt (Total Clearance)
4. Significance and Applications
These parameters help in determining dosing regimens, evaluating drug efficacy and safety, and designing drug delivery systems
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