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On Drug Substances
Author: Srikanth N
4/30/2012 1
http://stabilitystudies.blogspot.com
http://stabilitystudies.blogspot.com
Terminology
 Re-test date
 The date after which samples of the drug substance should be
examined to ensure that the material is still in compliance with the
specification and thus suitable for use in the manufacture of a given
drug product.
 Re-test period
 The period of time during which the drug substance is expected to
remain within its specification and, therefore, can be used in the
manufacture of a given drug product, provided that the drug substance
has been stored under the defined conditions.
 Primary batch
 A batch of a drug substance used in a formal stability study, from which
stability data are submitted in a registration application for the purpose
of establishing a re-test period .A primary batch of a drug substance
should be at least a pilot scale batch.
4/30/2012 http://stabilitystudies.blogspot.com 2
Terminology
 Mass balance
 The process of adding together the assay value and
levels of degradation products to see how closely these
add up to 100% of the initial value, with due
consideration of the margin of analytical error.
4/30/2012 http://stabilitystudies.blogspot.com 3
Objective
 Stability studies are conducted to assesses the effect of
Tempeature, Humidity and Light and to assign the
retest period and to recommend the storage
conditions.
4/30/2012 4
http://stabilitystudies.blogspot.com
Types
 Three types of Stability Studies
 Accelerated
 Studies designed to know the shortterm Excursions of
temperature on the drug Substances
 Intermediate
 Studies conducted, incase of failure in accelerated studies and
the conditions of temperature and humidity are in between
long term and accelerated.
 Long term
 Studies designed to check the stability of the drug substnace.
4/30/2012 5
http://stabilitystudies.blogspot.com
Stability Protocol
 Batch selection
 Container Closure System
 Specifications
 Testing frequency
 Storage conditions
 Sample Quanity
 Statements and labelling
 Stability commitment
4/30/2012 6
http://stabilitystudies.blogspot.com
Batch Selection
 Three Primary batches of drug susbtance are to be
kept for stability studies
 Usually three commercial batches to be kept in studies
and the batches may be first three batches.
 One add-on batch for every year. This might be the
first batch of that year
4/30/2012 7
http://stabilitystudies.blogspot.com
Container Closure System
 Stability Studies to be conducted in the container
closures that are similar to the containers in which the
Drug susbtance is marketting.
 For example, Itraconazole is stored in trasparent
polyethylene bag[primary packing] and which inturn
stored in black polyehtylene bag and finally in HDPE
container[secondary packing].
4/30/2012 8
http://stabilitystudies.blogspot.com
Specification
 Stability analysis is perfomed for the test parameters
which are prone to change during the storage and are
likely to influence the Qality, safety and Efficacy.
4/30/2012 9
http://stabilitystudies.blogspot.com
Testing Frequency
 Testing frequency for accelerated and long term as
follows
 Accelerated: 0,1,2,3 and 6 Months
 Long term: 0,3,6,9,12,18,24,36,48 and 60 Months
4/30/2012 10
http://stabilitystudies.blogspot.com
Storage Conditions
Type of study Accelerated Long term Intermediate
General
Case
40°C±2°C,
70±5% RH
25°C±2°C,
60±5% RH
30°C±2°C,
65±5% RH
Refrigeraed 25°C±2°C,
60±5% RH
5°C±3°C --
Freezer -20°C±5°C -- --
4/30/2012 11
http://stabilitystudies.blogspot.com
Sample Quantity
 Sample Quantity is determined on the analytical
parameters under study
Specification Accepatance
Crieteria
Quantity[G]
Description White to almost white
power
1 g [reusable]
Identification by IR Sample spectrum
should be
concorddant with that
of the sample
spectrum
300 mg
Loss on drying NMT 0.05% 1g
4/30/2012 12
http://stabilitystudies.blogspot.com
Sample Quantity
Specification Acceptance Crieteria Quantity{G}
Related Substances Monaamide impurity –NMT 0.15%
Dimer Impurity-NMT 0.15%
Unknown impurity-NMT 0.10%
Total Impurity-NMT 1,0%
1g
Assay by HPLC Between 98.0-102.0 % 1g
Total 3.3 g(rounded
to 4 g)
4/30/2012 13
http://stabilitystudies.blogspot.com
Sample Quantity
 For accelerated Studies
 Time points: 0,1,2,3 and 6 Months [Total 4 time point
excluding intial]
 For each time point: 4 g
 Total: 4 x 4 g = 16 g
 For Long term Studies
 Time points: 0,3,6,9,12,18,24,36,48 and 60 Months [Total
9 time point excluding intial]
 For each time point: 4 g
 Total: 9 x 4 g = 36 g
4/30/2012 14
http://stabilitystudies.blogspot.com
Sample Quantity
 Accelerated : 16 g+ 5 g extra= 21 g
 Long term: 36 g + 10g =46 g
 Total = 67 g [rounded to 70 grams]
4/30/2012 15
http://stabilitystudies.blogspot.com
Storage Statements and Labelling
Statement condition Label statement
25ºC / 60% RH (Long term)
40ºC / 75% RH (Accelerated term)
Do not store above 25°C
25ºC / 60% RH (Long term)
30ºC / 65% RH (Intermediate, failure
at long term)
Do not store above 25°C
30ºC / 65% RH (Long term)
40ºC / 75% RH (Accelerated term)
Do not store above 30ºC
5ºC +/- 3ºC Store in a refrigerator (2 to 8ºC)
-20ºC +/-5ºC Store in freezer
4/30/2012 16
http://stabilitystudies.blogspot.com
Stability Commitment
 It is commitment given to the reulatory authorities or
customers.
 All three batches of stability from production, studies
to be conducted through the assigned retest period.
 Less than 3 batches, commitment to add the
immediate prodcution batches to make 3 batches and
continue through the retest period assigned.
 No match from production, first three production
batches to be kept for stability studies continue
through the retest period assigned.
4/30/2012 17
http://stabilitystudies.blogspot.com
Stress Testing
 Stress testing of the drug substance can help identify the
likely degradation products, which can in turn help
establish the degradation pathways and the intrinsic
stability of the molecule and/or validate the stability
indicating power of the analytical procedures used.
 Stress testing to be carried out on a single batch of the drug
substance.
 Parameters in stress testing
 Acid Hydrolysis[0.1N HCl]
 Base Hydrolysis[0.1N NaoH]
 Oxidation[3% H2O2]
 Temperature with Humidity
 Photodegradation
4/30/2012 http://stabilitystudies.blogspot.com 18
Conditions
Study Chanllenge conditions Time Points
Acid/solution HCl (1.0N, RT, 70°C) Initial –7 days
Basic/Solution NaOH (1.0N, RT, 70°C) Initial –7 days
Oxidative/Solution H2O2+ Initiator 7 Days
Thermal 70°C/30% RH 6 weeks
Thermal/Humidity 70°C/75% RH 6 weeks
Photo (UV light)* 1,000 watt hrs/m2, RT 5 X ICH
Photo (Fluorescent
light)*
6 x 106 lux hrs, R.T. 5 X ICH
4/30/2012 http://stabilitystudies.blogspot.com 19
Others
 Stability Evaluation
 Data Variability and many more refer to
 http://stabilitystudies.blogspot.com
4/30/2012 20
http://stabilitystudies.blogspot.com

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stabilitystudies-120430065232-phpapp01.pdf

  • 1. On Drug Substances Author: Srikanth N 4/30/2012 1 http://stabilitystudies.blogspot.com http://stabilitystudies.blogspot.com
  • 2. Terminology  Re-test date  The date after which samples of the drug substance should be examined to ensure that the material is still in compliance with the specification and thus suitable for use in the manufacture of a given drug product.  Re-test period  The period of time during which the drug substance is expected to remain within its specification and, therefore, can be used in the manufacture of a given drug product, provided that the drug substance has been stored under the defined conditions.  Primary batch  A batch of a drug substance used in a formal stability study, from which stability data are submitted in a registration application for the purpose of establishing a re-test period .A primary batch of a drug substance should be at least a pilot scale batch. 4/30/2012 http://stabilitystudies.blogspot.com 2
  • 3. Terminology  Mass balance  The process of adding together the assay value and levels of degradation products to see how closely these add up to 100% of the initial value, with due consideration of the margin of analytical error. 4/30/2012 http://stabilitystudies.blogspot.com 3
  • 4. Objective  Stability studies are conducted to assesses the effect of Tempeature, Humidity and Light and to assign the retest period and to recommend the storage conditions. 4/30/2012 4 http://stabilitystudies.blogspot.com
  • 5. Types  Three types of Stability Studies  Accelerated  Studies designed to know the shortterm Excursions of temperature on the drug Substances  Intermediate  Studies conducted, incase of failure in accelerated studies and the conditions of temperature and humidity are in between long term and accelerated.  Long term  Studies designed to check the stability of the drug substnace. 4/30/2012 5 http://stabilitystudies.blogspot.com
  • 6. Stability Protocol  Batch selection  Container Closure System  Specifications  Testing frequency  Storage conditions  Sample Quanity  Statements and labelling  Stability commitment 4/30/2012 6 http://stabilitystudies.blogspot.com
  • 7. Batch Selection  Three Primary batches of drug susbtance are to be kept for stability studies  Usually three commercial batches to be kept in studies and the batches may be first three batches.  One add-on batch for every year. This might be the first batch of that year 4/30/2012 7 http://stabilitystudies.blogspot.com
  • 8. Container Closure System  Stability Studies to be conducted in the container closures that are similar to the containers in which the Drug susbtance is marketting.  For example, Itraconazole is stored in trasparent polyethylene bag[primary packing] and which inturn stored in black polyehtylene bag and finally in HDPE container[secondary packing]. 4/30/2012 8 http://stabilitystudies.blogspot.com
  • 9. Specification  Stability analysis is perfomed for the test parameters which are prone to change during the storage and are likely to influence the Qality, safety and Efficacy. 4/30/2012 9 http://stabilitystudies.blogspot.com
  • 10. Testing Frequency  Testing frequency for accelerated and long term as follows  Accelerated: 0,1,2,3 and 6 Months  Long term: 0,3,6,9,12,18,24,36,48 and 60 Months 4/30/2012 10 http://stabilitystudies.blogspot.com
  • 11. Storage Conditions Type of study Accelerated Long term Intermediate General Case 40°C±2°C, 70±5% RH 25°C±2°C, 60±5% RH 30°C±2°C, 65±5% RH Refrigeraed 25°C±2°C, 60±5% RH 5°C±3°C -- Freezer -20°C±5°C -- -- 4/30/2012 11 http://stabilitystudies.blogspot.com
  • 12. Sample Quantity  Sample Quantity is determined on the analytical parameters under study Specification Accepatance Crieteria Quantity[G] Description White to almost white power 1 g [reusable] Identification by IR Sample spectrum should be concorddant with that of the sample spectrum 300 mg Loss on drying NMT 0.05% 1g 4/30/2012 12 http://stabilitystudies.blogspot.com
  • 13. Sample Quantity Specification Acceptance Crieteria Quantity{G} Related Substances Monaamide impurity –NMT 0.15% Dimer Impurity-NMT 0.15% Unknown impurity-NMT 0.10% Total Impurity-NMT 1,0% 1g Assay by HPLC Between 98.0-102.0 % 1g Total 3.3 g(rounded to 4 g) 4/30/2012 13 http://stabilitystudies.blogspot.com
  • 14. Sample Quantity  For accelerated Studies  Time points: 0,1,2,3 and 6 Months [Total 4 time point excluding intial]  For each time point: 4 g  Total: 4 x 4 g = 16 g  For Long term Studies  Time points: 0,3,6,9,12,18,24,36,48 and 60 Months [Total 9 time point excluding intial]  For each time point: 4 g  Total: 9 x 4 g = 36 g 4/30/2012 14 http://stabilitystudies.blogspot.com
  • 15. Sample Quantity  Accelerated : 16 g+ 5 g extra= 21 g  Long term: 36 g + 10g =46 g  Total = 67 g [rounded to 70 grams] 4/30/2012 15 http://stabilitystudies.blogspot.com
  • 16. Storage Statements and Labelling Statement condition Label statement 25ºC / 60% RH (Long term) 40ºC / 75% RH (Accelerated term) Do not store above 25°C 25ºC / 60% RH (Long term) 30ºC / 65% RH (Intermediate, failure at long term) Do not store above 25°C 30ºC / 65% RH (Long term) 40ºC / 75% RH (Accelerated term) Do not store above 30ºC 5ºC +/- 3ºC Store in a refrigerator (2 to 8ºC) -20ºC +/-5ºC Store in freezer 4/30/2012 16 http://stabilitystudies.blogspot.com
  • 17. Stability Commitment  It is commitment given to the reulatory authorities or customers.  All three batches of stability from production, studies to be conducted through the assigned retest period.  Less than 3 batches, commitment to add the immediate prodcution batches to make 3 batches and continue through the retest period assigned.  No match from production, first three production batches to be kept for stability studies continue through the retest period assigned. 4/30/2012 17 http://stabilitystudies.blogspot.com
  • 18. Stress Testing  Stress testing of the drug substance can help identify the likely degradation products, which can in turn help establish the degradation pathways and the intrinsic stability of the molecule and/or validate the stability indicating power of the analytical procedures used.  Stress testing to be carried out on a single batch of the drug substance.  Parameters in stress testing  Acid Hydrolysis[0.1N HCl]  Base Hydrolysis[0.1N NaoH]  Oxidation[3% H2O2]  Temperature with Humidity  Photodegradation 4/30/2012 http://stabilitystudies.blogspot.com 18
  • 19. Conditions Study Chanllenge conditions Time Points Acid/solution HCl (1.0N, RT, 70°C) Initial –7 days Basic/Solution NaOH (1.0N, RT, 70°C) Initial –7 days Oxidative/Solution H2O2+ Initiator 7 Days Thermal 70°C/30% RH 6 weeks Thermal/Humidity 70°C/75% RH 6 weeks Photo (UV light)* 1,000 watt hrs/m2, RT 5 X ICH Photo (Fluorescent light)* 6 x 106 lux hrs, R.T. 5 X ICH 4/30/2012 http://stabilitystudies.blogspot.com 19
  • 20. Others  Stability Evaluation  Data Variability and many more refer to  http://stabilitystudies.blogspot.com 4/30/2012 20 http://stabilitystudies.blogspot.com