This document provides an overview of bioavailability, bioequivalence, and BCS classification. It defines key terms like bioavailability, absolute and relative bioavailability, and factors affecting bioavailability. Measurement methods like pharmacokinetic and pharmacodynamic approaches are discussed. Bioequivalence studies and their types are summarized. The six classes of BCS classification and its applications in drug development are highlighted in brief. In conclusion, the document notes that BCS classification provides guidance in drug formulation and review processes to reduce costs and time of approval.
It is defined as “the predictive mathematical model that describes the relationship between in vitro property (such as rate & extent of dissolution) of a dosage form and in vivo response (such as plasma drug concentration or amount of drug absorbed)”.
It is defined as “the predictive mathematical model that describes the relationship between in vitro property (such as rate & extent of dissolution) of a dosage form and in vivo response (such as plasma drug concentration or amount of drug absorbed)”.
It includes Introductory part about what is Dissolution...then Mechanism of Dissolution is elaborated...Theories of Dissolution also given..It also includes Factors affecting Dissolution profile..Along with References given below for easily searching..
In this slide contains introduction, copmpression, consolidation, compaction, heckel plots and equation, interpretation and application.
Presented by: NARAYAN SINGH UDIT (Department of pharmaceutics).
RIPER, anantapur
An in-vitro in-vivo correlation (IVIVC) has been defined by the U.S. Food and Drug Administration (FDA) as "a predictive mathematical model describing the relationship between an in-vitro property of a dosage form and an in-vivo response".
Gastrointestinal tract, Mechanism of drug absorption, Factors
affecting drug absorption, pH–partition theory of drug absorption. Formulation and physicochemical factors: Dissolution rate, Dissolution process, Noyes–Whitney equation and drug dissolution, Factors affecting the dissolution rate. Gastrointestinal absorption: Role of the dosage form: Solution (elixir, syrup and solution) as a dosage form ,Suspension as a dosage form, Capsule as a dosage form, Tablet as a dosage form ,Dissolution methods ,Formulation and processing factors, Correlation of in vivo data with in vitro dissolution data. Transport model: Permeability-Solubility-Charge State and the pH Partition Hypothesis, Properties of the Gastrointestinal Tract (GIT), pH Microclimate Intracellular pH Environment, Tight Junction Complex.
It includes Introductory part about what is Dissolution...then Mechanism of Dissolution is elaborated...Theories of Dissolution also given..It also includes Factors affecting Dissolution profile..Along with References given below for easily searching..
In this slide contains introduction, copmpression, consolidation, compaction, heckel plots and equation, interpretation and application.
Presented by: NARAYAN SINGH UDIT (Department of pharmaceutics).
RIPER, anantapur
An in-vitro in-vivo correlation (IVIVC) has been defined by the U.S. Food and Drug Administration (FDA) as "a predictive mathematical model describing the relationship between an in-vitro property of a dosage form and an in-vivo response".
Gastrointestinal tract, Mechanism of drug absorption, Factors
affecting drug absorption, pH–partition theory of drug absorption. Formulation and physicochemical factors: Dissolution rate, Dissolution process, Noyes–Whitney equation and drug dissolution, Factors affecting the dissolution rate. Gastrointestinal absorption: Role of the dosage form: Solution (elixir, syrup and solution) as a dosage form ,Suspension as a dosage form, Capsule as a dosage form, Tablet as a dosage form ,Dissolution methods ,Formulation and processing factors, Correlation of in vivo data with in vitro dissolution data. Transport model: Permeability-Solubility-Charge State and the pH Partition Hypothesis, Properties of the Gastrointestinal Tract (GIT), pH Microclimate Intracellular pH Environment, Tight Junction Complex.
Bio pharmaceutical classification System [BCS]Sagar Savale
The Biopharmaceutical Classification System was first developed by in 1995, by Amidon et al & his colleagues.
Definition:
“The Biopharmaceutical Classification System is a scientific framework for classifying a drug substance based on its aqueous solubility & intestinal permeability & dissolution rate”.
To saved time fast screening is required so drug substances are classified on basis of solubility and permeability. This classification is called Biopharmaceutical Classification System
Biopharmaceutics Classification System (BCS) & Waiver of BioequivalenceAjaz Hussain
Graduate Lecture at the University of Maryland (August 2012). Learning Objective: Identify and explain how future regulatory applications of BCS may be realized in the context of ‘Quality by Design’.
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2. Change permeability boundary from 90% to 85%
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OMICS Publishing Group, Journal of Bioequivalence & Bioavailability provides an immediate Open Access to its content making research freely available to the public which supports a greater global exchange of knowledge in the chemical and pharmacological areas.
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“ Bioavailability-
means the rate and extent to which the active ingredient or active moiety is absorbed from a drug product and becomes available at the site of action."
Methods For Assesment Of Bioavailability Anindya Jana
Bioavailability means the rate and extent to which the active ingredient or active moiety is absorbed from a drug product and becomes available at the site of action. 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.
Bioavailability studies are important in the Primary stages of development of a suitable dosage form for a new drug entity, determination of influence of excipients, patient related factors & possible interaction with other drugs on the efficiency of absorption, development of new formulations of the existing drugs, control of quality of a drug product during the early stages of marketing in order to determine the influence of processing factors, storage & stability on drug absorption
It contain the Per oral administration of drug ,
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4. Regulatory Definition
(21 CFR 320.1(a)):
“Bioavailability means the
rate and extent to which the active ingredient or
active moiety is absorbed from a drug product
and becomes available at the site of action.”
4
5. Primary stages of development of a suitable dosage form for
new drug entity.
Determination of influence of excipients, patient related factors
and interaction with other drugs on the efficiency of absorption.
To evaluate the absolute systemic availability of active drug
substance from a dosage form.
Control quality of drug in early stages of development.
Develop new formulation for existing drug.
5
6. Systemic availability the amount that reaches
systemic circulation is simply known as availability.
Absolute bioavailability of a drug product may be
comparing the respective bioavailabilites after an
oral and iv bolus injection.
Relative bioavailability is defined as a ratios of
bioavilabilities of a drug product and reference
standard.
6
10. The methods available are:Pharmacokinetic (Indirect) Method
Pharmacodynamic (Direct) Method.
Selection of method depends upon :Nature Of The Study
Nature Of Dosage Form
Analytical Method Development.
10
13. Cmax
- Maximum plasma concentration .
The concentration of drug at therapeutic response is elicited.
Increase with increase in dose and with an increase in absorption.
Tmax
- Time to reach maximum concentration
Indicates rate of absorption.
It decrease as the rate of absorption increases.
AUC - Area under the curve.
Indicates the extent of drug absorption from a dosage form.
The fraction of dose that reaches the systemic circulation.
13
15. Maximum urinary excretion rate
It is obtained from peak of plot between rate of urinary
excretion data versus time.
Time for maximum excretion rate
It is the maximum time required to reach maximum excretion
rate.
Cumulative amount of drug excreted
It is the drug excreted in urine till the drug level falls zero.
15
16. Sl. no
Plasma data
Urinary data
1.
Maximum plasma
concentration
C max
Time to maximum
concentration
T max
Area under the curve
AUC
Maximum urinary excretion
rate
2.
3.
Time to maximum
excretion rate
Cumulative amount of drug
excreted
16
18. Acute pharmacological response
When bioavailability measurement by pharmacokinetic method is
difficult, an acute pharmacologic effect are taken into consideration
Dose
response
curve
Can
be
determined
by
construction
of
Pharmacological effect Vs Time curve
E.g.: pupil diameter, heart rate or BP can be useful as an index of drug
bioavailability
Clinical response / Therapeutic response
Best method Clinical response of the drug for which it is intended to be
used is measured
Based on clinical response to the drug formulation given to the patients
E.g.: for anti-inflammatory drugs, reduction in inflammation is determined
18
20. Bioequivalence
When the drug from two or more similar dosage form
reaches the general circulation at the same relative rate
and extent then the dosage forms are termed as
Bioequivalent.
Statistical significant differences are observed in the
bioavailability
of
Bio-inequivalence.
two
or
more
drug
products,
20
21. When significant changes are made in the manufacture of the
marketed formulation
When a new generic formulation is tested against the
innovator's marketed product
Comparison of availability of drug substance from different
dosage forms
when changes in formulation have occurred after an
innovator product has been approved.
Comparison of availability's of same dosage form produced
by different manufactures
21
26. Valuable tool for formulation scientist for selection of
design of formulated drug substance.
Efficiency of drug development and review process.
To Reduces cost and time of approving Scale- up and post
approval challenges.
Applicable
in
both
pre-clinical
and
clinical
drug
development process.
Works as a guiding tool in development of various oral drug
delivery systems.
26
27. It’s a theoretical basis for correlating in vitro drug dissolution
with in vivo availability, developed by Dr. Gordon Amidon et
al(1995) and submitted at FIP, Brazil.
Based on Aqueous solubility and intestinal permeability.
Classification on Fick’s first law
J w = Pw C w
Where J w = Drug flux across the GUT wall
Pw = Permeability of membrane
C w = Drug concentration at GI membrane
27
29. Sl. no
Class of drug
solubility
permeability
1
Ia
High and site
independent
High and site
independent
2
Ib
High and site
independent
Depend on site and
narrow therapeutic
window
3
II a
Low and site
independent
High and site
independent
4
II b
Low and site
independent
Depend on site and
narrow therapeutic
window
5
V a : acidic
Variable
variable
6
V b : basic
Variable
variable
29
30. Berstrom
et
al
(2003) modified BCS to six classes
Development is based on calculated surface area, solubility
and permeability.
Based on solubility and permeability was classified into 6
classes as low, intermediate and high.
Based on surface area Non-polar part - good solubility, Polar
part – good permeability.
Three compounds are wrongly classified amitryptiline,
acyclovir and doxycycline
30
31. Applications in both pre - clinical and clinical drug
development.
Regulatory toll for replacement of certain be studies.
Reduces the time in the drug development process as
time is an important aspect in industry.
Leads to direct and indirect savings of pharmaceutical
companies.
31
32. Solubility profile should be determined
PH range of 1-7.5 at 37
1 c.
The drug is said to be highly soluble in a solution with
defined pH when the highest dose is soluble in 250ml of
aqueous media over pH range of 1-7.5.
Shake flask method is used to for invitro determination of
solubility.
E.g. Acid or base titration methods.
32
33. Sl. No
Terms
Parts Of Solute Required To
Dissolve One Part Of Solvent
1.
2.
3.
Very Soluble
Freely Soluble
Soluble
Less Than 1 Part
1 To 10 Part
10 To 30 Part
4.
5.
6.
Sparingly Soluble
Slightly Soluble
Very Slightly Soluble
Practically Insoluble Or
Insoluble
30 To 100 Part
100 To 1000 Part
1000 To 10,000 Part
7.
More Than 10,000 Part
33
34. Highly permeable is said to be when the
extent of absorption is determined 90% or more than it
Human studies include mass balance studies, absolute
bioavailability, intestinal perfusion methods in vivo studies
Drug absorption
Prediction in humans is by In vitro
permeability by intestinal tissue and mono layer of epithelial
cells
E.g. Caco – 2cells or TC – 7
34
35. There are some methods to determine permeability of drug in
GI track include
1. In vivo intestinal perfusion studies in humans
2. In vivo intestinal perfusion studies in animals
3. In vitro permeation in experiments using excised human or
animal tissue intestinal tissue
4. In vitro permeation experiments across monolayer of
cultured human intestinal cells.
35
36. Dissolution class includes IR product following
conditions to be applied
Dissolving not less than 85% amount of drug with in
30 min
Using USP Dissolution apparatus 1 at 100 rpm in a
volume of 900ml or less
In 0.1 N HCl or simulated gastric fluid or PH 4.5
buffer and PH 6.8 buffer or stimulated intestinal fluid.
36
37. (FDA Guidelines for industry , 2000; Adomin et al, 1995)
Applicable in NDA’s, ANDA’s and post approval changes.
Primary evidence of safety and efficacy.
Significant in pre and post approval changes in
pharmaceutical equivalents.
BCS eliminates the need human subjects to reference and
test products.
37
38. Conclusions
Every drug in the development process must undergo BABE
studies.
Primary stages of drug development and formulation of
dosage includes Bioavailability.
Presently, there is international harmonization of regulatory
requirements for bioequivalence studies
BCS eliminates unnecessary drugs exposures to healthy
subjects and provides economic relief and maintain high
public standard for therapeutic equivalence.
38
39. Previous GPAT Bits Covered In
This Topic
A drug (200 mg dose) administered in tablet form and as intravenous
injection (50 mg dose) showed AUC of 100 and 200 microgram hr/mL,
respectively. The absolute availability of the drug through oral
administration is : (GPAT 2012)
(A) 125% (B) 250 % (C) 12.5% (D) 1.25%
Half life is the time it takes for the concentration of drug to halve, no matter
what the starting concentration is. If the drug is eliminated by First order
kinetics how many half-lives it takes for a drug for total elimination of 97%
of drug (GPAT 2010)
a)
3 half-lives B) 5 half-lives
C) 8 half-lives
D) 10 half-lives
39
40. Previous GPAT Bits Cover In This
Topic (cont….)
The characteristic of non-linear pharmacokinetics include ( GPAT 2011)
(A) Area under the curve is proportional to the dose
(B) Elimination half-life remains constant,
(C) Area under the curve is not proportional to the dose
(D) Amount of drug excreted through remains constant
The percentage of a dose of drug product administered via extravascular
route that is systemically available as compared to an intravenous dose is
referred as (GPAT 2010)
A) Absolute bioavailability
C) AUC
B) Relative bioavailability
D) T max
40
41. Previous GPAT Bits Cover In This
Topic (cont….)
Which conditions does not apply as per Indian lw while conducting
single dose bioavailability study of an immediate release product?
(GPAT 2011)
a)
Sampling Period should be at least three t ½ el
b) Sampling should represent pre-exposure, peak exposure and post
exposure phases.
c) There should be at least four sampling points during elimination
phase
d) Sampling should be continued till measured AUC is at least equal
to 80% of AUC
41
42. List Of References
Guidelines for bioavailability and bioequivalence studies,
CDSCO, directorate general of health service, Ministry of family and health
welfare, new Delhi.
Applied Biopharmaceutics and pharmacokinetics, 6th edition, pg no 431-433 –
leon shargel
Remington the scientists practice of pharmacy 21st edition, vol 1 1037-1046
Biopharmaceutics and clinical pharmacokinetics 4th edition, pg no 3, 352,171 –
robert notori
Biopharmaceutics and pharmacokinetics a treatise pg no- 315-363, - DM
Bramankar
Biopharmaceutics and clinical pharmacokinetics – pg 7-9, 146-175, milo gibadi
Martins physical pharmacy and pharmaceutical sciences 6th edition pg no -232
42
43. List Of References (cont…..)
Biopharmaceutics and pharmacokinetics pg no 331-356, - v. venkateshvarulu
Biopharmaceutics classification a strategic tool for classifying drug substances
ISSN 2230-8407 – rohila seema www.irjponline.com
What is bioavailability and bioequivalence Candida agency for drug and technology
for health www.cadth.generics/ca
Bioavailability and Bioequivalence- Jake J. Thiessen, Ph.D, University of Toront,
Canada, Email jj.thiessen@utoronto.ca
Bioavailability and Bioequivalence Studies, “ Standard Approach”, www.ivivc.com
Bioavailability & bioequivalence trials, Shubha Rani, Ph.D, Synchron Research
Services Pvt. Ltd., Ahmadabad, drshubha@synchronresearch.com
43
44. Acknowledgement
I sincerely thank and regards
to my guide K. Pallavi, and
other staff members for their
support. I would also thank
my
family,
friends
and
finally our beloved Principal
Dr. P. Srinivasa Babu.
44