This document provides an overview of key pharmacokinetic concepts including bioavailability, Cmax, distribution, half-life, Tmax, and area under the curve (AUC). Bioavailability describes the amount of drug that reaches systemic circulation. Cmax is the maximum drug concentration in blood plasma. Distribution describes drugs binding to plasma proteins. Half-life is the time for drug concentration to reduce by half. Tmax is the time to reach Cmax. AUC represents total drug absorption over time.
PHARMACOKINETIC MODELS
Drug movement within the body is a complex process. The major objective is therefore to develop a generalized and simple approach to describe, analyse and interpret the data obtained during in vivo drug disposition studies.
The two major approaches in the quantitative study of various kinetic processes of drug disposition in the body are
Model approach, and
Model-independent approach (also called as non-compartmental analysis).
PHARMACOKINETIC MODELS
Drug movement within the body is a complex process. The major objective is therefore to develop a generalized and simple approach to describe, analyse and interpret the data obtained during in vivo drug disposition studies.
The two major approaches in the quantitative study of various kinetic processes of drug disposition in the body are
Model approach, and
Model-independent approach (also called as non-compartmental analysis).
DISSOLUTION
Dissolution is defined as a process in which a solid substance solubilises in a given solvent.
(i.e. mass transfer from the solid surface to the liquid phase.)
Three Theories:
Diffusion layer model / Film theory
Danckwert’s model / Penetration or Surface renewal theory
Interfacial barrier model / Double barrier or Limited solvation theory
This presentation is about the process by which prolonged therapeutic activity of drug is achieved and it's importance. By this presentation you will learn about dosage regimen, steady state concentration, principle of superposition, drug accumulation, repetitive intravenous injections etc. By this you will also learn how to adjust the dose to the patient.
1. Measurement of Bioavailability:
Direct and indirect methods may be used to assess drug bioavailability. The in-vivo bioavailability of a drug product is demonstrated by the rate and extent of drug absorption, as determined by comparison of measured parameters, e.g., concentration of the active drug ingredient in the blood, cumulative urinary excretion rates, or pharmacological effects.
For drug products that are not intended to be absorbed into the bloodstream, bioavailability may be assessed by measurements intended to reflect the rate and extent to which the active ingredient or active moiety becomes available at the site of action.
The design of the bioavailability study depends on the objectives of the study, the ability to analyze the drug (and metabolites) in biological fluids, the pharmacodynamics of the drug substance, the route of drug administration, and the nature of the drug product.
Pharmacokinetic and/or pharmacodynamic parameters as well as clinical observations and in-vitro studies may be used to determine drug bioavailability from a drug product.
1.1. Pharmacokinetic methods:
These are very widely used and based upon the assumption that the pharmacokinetic profile reflects the therapeutic effectiveness of a drug. Thus these are indirect methods. The two major pharmacokinetic methods are:
The major pharmacokinetic methods are:
Plasma / blood level time profile.
o Time for peak plasma (blood) concentration (t max)
o Peak plasma drug concentration (Cmax)
o Area under the plasma drug concentration–time curve (AUC)
Urinary excretion studies.
o Cumulative amount of drug excreted in the urine (Du)
o Rate of drug excretion in the urine (dDu/dt)
o Time for maximum urinary excretion (t)
C. Other biological fluids
1.2. Pharmacodynamic methods:
IT involves direct measurement of drug effect on a (patho) physiological process as a function of time. Disadvantages of it may be high variability, difficult to measure, limited choices, less reliable, more subjective, drug response influenced by several physiological & environmental factors.
They involve determination of bioavailability from:
Acute pharmacological response.
Therapeutic response.
1.3. In-vitro dissolution studies
Closed compartment apparatus
Open compartment apparatus
Dialysis systems.
1.4. Clinical observations
Well-controlled clinical trials
KINETICS OF MULTIPLE DOSING under the Unit Multicompartment Models According to New PCI syllabus 2017 by Ms. Preeti Patil-Vibhute, Assistant Professor, Sarojini College of Pharmacy, Kolhapur.
DISSOLUTION
Dissolution is defined as a process in which a solid substance solubilises in a given solvent.
(i.e. mass transfer from the solid surface to the liquid phase.)
Three Theories:
Diffusion layer model / Film theory
Danckwert’s model / Penetration or Surface renewal theory
Interfacial barrier model / Double barrier or Limited solvation theory
This presentation is about the process by which prolonged therapeutic activity of drug is achieved and it's importance. By this presentation you will learn about dosage regimen, steady state concentration, principle of superposition, drug accumulation, repetitive intravenous injections etc. By this you will also learn how to adjust the dose to the patient.
1. Measurement of Bioavailability:
Direct and indirect methods may be used to assess drug bioavailability. The in-vivo bioavailability of a drug product is demonstrated by the rate and extent of drug absorption, as determined by comparison of measured parameters, e.g., concentration of the active drug ingredient in the blood, cumulative urinary excretion rates, or pharmacological effects.
For drug products that are not intended to be absorbed into the bloodstream, bioavailability may be assessed by measurements intended to reflect the rate and extent to which the active ingredient or active moiety becomes available at the site of action.
The design of the bioavailability study depends on the objectives of the study, the ability to analyze the drug (and metabolites) in biological fluids, the pharmacodynamics of the drug substance, the route of drug administration, and the nature of the drug product.
Pharmacokinetic and/or pharmacodynamic parameters as well as clinical observations and in-vitro studies may be used to determine drug bioavailability from a drug product.
1.1. Pharmacokinetic methods:
These are very widely used and based upon the assumption that the pharmacokinetic profile reflects the therapeutic effectiveness of a drug. Thus these are indirect methods. The two major pharmacokinetic methods are:
The major pharmacokinetic methods are:
Plasma / blood level time profile.
o Time for peak plasma (blood) concentration (t max)
o Peak plasma drug concentration (Cmax)
o Area under the plasma drug concentration–time curve (AUC)
Urinary excretion studies.
o Cumulative amount of drug excreted in the urine (Du)
o Rate of drug excretion in the urine (dDu/dt)
o Time for maximum urinary excretion (t)
C. Other biological fluids
1.2. Pharmacodynamic methods:
IT involves direct measurement of drug effect on a (patho) physiological process as a function of time. Disadvantages of it may be high variability, difficult to measure, limited choices, less reliable, more subjective, drug response influenced by several physiological & environmental factors.
They involve determination of bioavailability from:
Acute pharmacological response.
Therapeutic response.
1.3. In-vitro dissolution studies
Closed compartment apparatus
Open compartment apparatus
Dialysis systems.
1.4. Clinical observations
Well-controlled clinical trials
KINETICS OF MULTIPLE DOSING under the Unit Multicompartment Models According to New PCI syllabus 2017 by Ms. Preeti Patil-Vibhute, Assistant Professor, Sarojini College of Pharmacy, Kolhapur.
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Pharmacokinetics, sometimes described as what the body does to a drug, refers to the movement of drug into, through, and out of the body—the time course of its absorption, bioavailability, distribution, metabolism, and excretion.
Expt. 13 Calculation of pharmacokinetic parameters from a given dataVISHALJADHAV100
Objective
Pharmacokinetics (PKs) and Clinical Pharmacokinetics
Plasma Drug Concentration-Time Profile
Peak Plasma Concentration (Cmax)
Time of Peak Concentration (tmax)
Area Under the Curve (AUC)
Bioavailability (BA)
Volume of Distribution (Vd)
Half-Life (t1/2)
Clearance (CL)
Loading and Maintenance Dose
Result and interpretation
The study of the disposition of a drug
It includes the processes of ADME
Absorption
Distribution
Metabolism
Excretion
Toxicity
Patients may suffer
Toxic drugs may accumulate
Useful drugs may have no benefit because doses are too small to establish therapeutic efficacy
A drug can be rapidly metabolized
Absorption is the process by which a drug enters the bloodstream without being chemically altered
Factors which influence the rate of absorption
types of transport
the physicochemical properties of the drug
protein binding
routes of administration
dosage forms
circulation at the site of absorption
concentration of the drug
Lecture Presentation in Basic Intravenous Therapy Seminar talks on Basic Pharmacology, the pharmacodynamics and pharmacokinetics, the common IV medications used, precautions and interactions of medications
1.0.bioavailability, pharmacokinetics and efficacy determinationsalummkata1
Bioavailability is a measure of the rate and fraction of the initial dose of a drug that successfully reaches either; the site of action or the bodily fluid domain from which the drug’s intended targets have unimpeded access.
For majority purposes, bioavailability is defined as the fraction of the active form of a drug that reaches systemic circulation unaltered. This definition assumes 100% of the active drug that enters systemic circulation will successfully reach the target site. However, it should be appreciated that this definition is not inclusive of drugs that do not require access to systemic circulation for function (i.e., certain topical drugs). The bioavailability of these drugs is measured by different parameters discussed elsewhere.
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Links to PowerPoint presentations in poultry diseases, medications, and immunity in addition to soft skills courses
Share to benefit others
ادوية علاج الدواجن من المضادات الحيوية ومستخلصات الأعشاب
Poultry medications (antibiotics and herbal extracts)
Link to download more presentations in powerpoint
https://lnkd.in/gJGGnPY
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Link to download presentations in powerpoint
https://lnkd.in/g2ef7DP
كورسات التنمية البشرية
Soft skills courses
Link to download presentations in powerpoint
https://lnkd.in/g8W7TYq
Presentations are continuously updated
المكتبة متجددة باستمرار
البوست ده عمل خيري ...
دي لينكات لمحاضرات في امراض وادوية الدواجن وكورسات التنمية البشرية ... جميع المحاضرات بصيغة بوربوينت
شير لعلها تكون المنجية لنا جميعا
This post is for charity ...
Links to PowerPoint presentations in poultry diseases, medications, and immunity in addition to soft skills courses
Share to benefit others
ادوية علاج الدواجن من المضادات الحيوية ومستخلصات الأعشاب
Poultry medications (antibiotics and herbal extracts)
Link to download more presentations in powerpoint
https://lnkd.in/gJGGnPY
امراض الدواجن البكتيرية والفيروسية واساسات التحصينات ومناعة الطيور
Poultry diseases, vaccination and immunity
Link to download presentations in powerpoint
https://lnkd.in/g2ef7DP
كورسات التنمية البشرية
Soft skills courses
Link to download presentations in powerpoint
https://lnkd.in/g8W7TYq
Presentations are continiously updated
المكتبة متجددة باستمرار
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Link to download more presentations in PowerPoint
https://drive.google.com/open?id=1EtFtygmlvOYqjqpanRTIgoExIENd-YIB
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Link to download presentations in PowerPoint
https://drive.google.com/open?id=1znC0qeHMivV2ai4_IUweA-VTBQLJSVKu
كورسات التنمية البشرية
Soft skills courses
Link to download presentations in PowerPoint
https://drive.google.com/open?id=1R3CqcFO10bOyi1aRQx0WNSn6B5TMNMxu
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7. C MAX
C MAX describes the maximum concentration a drug reaches in
the blood plasma.
High C MAX indicates:
1. Better absorption.
2. Higher bioavailability.
3. Less doses (based on HALF LIFE)
9. DISTRIBUTION
Once in the circulation, some drugs bind non specifically
and reversibly to various plasma protein; that is, to albumin
or globulin.
Only the free drug exerts a biological effect; the bound
drug stays in the vascular space and is not metabolized or
eliminated.
12. T MAX
T MAX describes the time needed to reach the C MAX.
Short T MAX indicates:
1. Rapid onset of action.
2. More doses (based on HALF LIFE)
Long T MAX indicates:
1. Delayed onset of action.
2. Less doses (based on HALF LIFE)
15. HALF LIFE
HALF-LIFE is the time required for the C MAX to decrease to half
of its initial value.
Long half life indicates:
1. Less doses (based on C MAX)
17. AUC
AREA UNDER THE TIME CONCENTRATION CURVE
TIME
CONCENTRATION
C MAX
T MAX
x HALF-LIFE
AREA UNDER THE CURVE
18. AUC
AREA UNDER THE TIME CONCENTRATION CURVE
AUC represents the total amount of drug absorbed by the body,
irrespective of the rate of absorption.
AUC becomes useful for:
1. Knowing the average concentration over a time
interval.
2. Knowing the elimination rate.