best practices for leachables and extractables testing...best practices for leachables and...
TRANSCRIPT
![Page 1: Best Practices for Leachables and Extractables Testing...Best Practices for Leachables and Extractables Testing Daniel L. Norwood, PhD IPAC-RS Chair – PQRI Leachables and Extractables](https://reader036.vdocument.in/reader036/viewer/2022062312/610f514c2ba8764ddc1e60a6/html5/thumbnails/1.jpg)
Best Practices for Leachables and Extractables Testing
Daniel L. Norwood, PhDIPAC-RS
Chair – PQRI Leachables and ExtractablesWorking Group
PQRI Leachables and Extractables WorkshopBethesda, MD
5 December 2005
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Presentation Outline
• Why produce “Best Practice”recommendations?
• The Working Group’s hypothesis
• Laboratory work in support of recommendations
• Recommendation areas
• Introduction to recommendation specifics
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Why Produce “Best Practice” Recommendations?
• To reduce uncertainty in the pharmaceutical development process for OINDP.
• To reduce or eliminate “Horror Stories” .
• To support Agency initiatives, such as Quality by Design and Risk Management.
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Simulated Project Team Meeting
Can’t we all just get along?
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Simulated Encounter with Senior Management
Simulated Project Team
Leader
Simulated VPBut it was a
Project Team decision!!!!
Simulated NDA
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The Working Group’s Hypothesis
1. Scientifically justifiable thresholds based on the best available data and industry practices can be developed for:
a. the reporting and safety qualification of leachables in orally inhaled and nasal drug products, and
b. reporting of extractables from the critical components used in corresponding container/closure systems.
Reporting thresholds for leachables and extractables will include associated identification and quantitation thresholds.
2. Safety qualification of extractables, would be scientifically justified on a case-by-case basis.
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Laboratory Work• Volunteer laboratories
• Custom made “Test Articles” (3 elastomers and one plastic, all with known formulations)
• Two Phases of extractables work (both protocol driven):
• Phase 1 – Qualitative Controlled Extraction Studies
• Phase 2 – Analytical Method Optimization/Validation
• Placebo leachables studies
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Chemistry: Volunteer Laboratories
• Boehringer Ingelheim Pharmaceuticals, Inc.• Cardinal Health (Magellan Laboratories)• CIBA Expert Services• Merck and Company, Inc• West Monarch Analytical Laboratories• PPD• Valois, Inc• West Pharmaceutical Services• FDA• Owens Illinois• Chevron Phillips
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Rubber Formulation A (Sulfur Cured)Ingredient %
CALCINED CLAY 8.96BLANC FIXE (barium sulfate) 25.80CREPE 38.22BROWN SUB MB 16.841722 MB 2.11
ZINC OXIDE 4.042, 2’ METHYLENE-BIS (6-TERTIARY BUTYL-4-ETHYL PHENOL) 0.56COUMARONE-INDENE RESIN 1.12PARAFFIN 1.12TETRAMETHYLTHIURAM MONOSULFIDE 0.11ZINC 2-MERCAPTOBENZOTHIAZOLE 0.29SULFUR 0.84
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Polypropylene Formulation
Ingredient wt %
• Primary StabilizersTetrakis (methylene(3,5-di-t-butyl-4-hydroxyhydrocinnamate)) methane
Irganox 1010 (Ciba) 0.08 wt%Anox 20 (Great Lakes)
• Secondary StabilizersBis(2,4-di-t-butylphenyl)pentaerythritol diphosphite
Ultranox 626 (GE) 0.05 wt%
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Polypropylene FormulationIngredient wt %
• Corrosion InhibitorsCalcium Stearate 114-50 (Ferro) 0.03 - 0.4 wt%
• AntistaticVegetable oil derived 90% alpha monoglycerides (soybean) Pationic 901 (Patco) 0.3 wt%Dimodan HS-KA (Danisco)
• Nucleating Agents3,4 -dimethyl dibenzylidene sorbitolMillad 3988 (Milliken) 0.2 wt%
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State-of –the-Art InstrumentationState-of –the-Art Instrumentation
X
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A “Modern” LC/MS SystemA “Modern” LC/MS System
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Chemistry: Phase 1 Studies
• Controlled Extraction Studies
• Multiple solvents with differing polarities:
– Dichloromethane, 2-propanol, hexane
• Multiple extraction techniques
– Sonication, Soxhlet, reflux
• Multiple analytical techniques
– GC/MS, LC/UV (DAD), LC/MS
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Representative Extraction Apparatus
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GC/MS Extractables Profile of the Sulfur-Cured Elastomer
5.00 10.00 15.00 20.00 25.00 30.00 35.000
500000
1000000
1500000
2000000
2500000
3000000
3500000
4000000
4500000
5000000
5500000
6000000
6500000
7000000
7500000
8000000
8500000
9000000
9500000
1e+07
1.05e+07
1.1e+07
1.15e+07
1.2e+07
1.25e+07
1.3e+07
1.35e+07
Time-->
Abundance
TIC: 02050302.D
24 hr Soxhlet extractionIn methylene chloride
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GC/MS Extractables Profile of Valois Elastomer Methylene Chloride Soxhlet Extract
5.00 10.00 15.00 20.00 25.00 30.00 35.00
500000
1000000
1500000
2000000
2500000
3000000
3500000
4000000
4500000
5000000
5500000
6000000
6500000
7000000
Time-->
Abundance
TIC: 08190302.D
BHTI.S.
C16
C182246
Irganox 1076
PeroxideFrags.?
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LC/MS Extractables Profile of Polypropylene Methylene Chloride Reflux Extract
Reflux PP Disc/CH2Cl2
5.00 10.00 15.00 20.00 25.00 30.00 35.00 40.00 Time 0
100
%
0
100
%
03270311 280 nm ANALOG
5.22e5 10.55
5.34
8.44
20.92
18.90 33.92
03270311 Scan AP- TIC
1.27e7 18.36
10.64
5.02 3.17 8.55
16.02
13.50
20.25
34.01
25.63 31.38 40.31 37.86 44.91
11
12
9
6
4
8
7
2
4
9
12
3
3 5 10
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Chemistry: Phase 2 Studies
• Sulfur-cured elastomer (Ciba)– Completed optimization of extractions using Soxhlet
extraction with methylene chloride
– Completed validation on GC/FID method
– Details available in poster presentation
• Polypropylene (West Monarch)– Completed optimization of extractions using reflux in
isopropanol and THF
– Completed validation of LC/UV method
– Details available in poster presentation
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SULFUR-CURED ELASTOMER EXTRACTABLES
PQRI Extractives Phase II Exp. 2
0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
0.9
1
0 2 4 6 8 10 12 14 16 18
Time, hours
Are
a ra
tio, a
naly
te to
IS
Phenolic
Docosane
Hexacosane
Coumarone indene
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Placebo Leachables Study
• Samples contained in formulation development bottles (plastic coated)
• CFC-11• Sulfur-cured elastomer
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Laboratory Scale Stability Chamber
• Note inner door• Note placebo
leachables study in storage
• 40°C/75%RH• 3 months storage
anticipated
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Leachables Profile – 1 Week Timepoint
5.00 10.00 15.00 20.00 25.00 30.00 35.000
1000000
2000000
3000000
4000000
5000000
6000000
7000000
8000000
9000000
1e+07
1.1e+07
1.2e+07
1.3e+07
1.4e+07
Time-->
Abundance
TIC: 11100303.D
I.S. 40µg/canister
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Leachables Profile – 1 Week TimepointExpanded
5.00 10.00 15.00 20.00 25.00 30.00 35.00
100000
200000
300000
400000
500000
600000
700000
800000
900000
1000000
1100000
1200000
Time-->
Abundance
TIC: 11100303.D
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Recommendation Areas
• Container/Closure System Components –Composition and Selection
• Controlled Extraction Studies
• Leachables Studies and Routine Extractables Testing
• The Analytical Evaluation Threshold (AET)
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Specific Questions Addressed
1. What does it mean to “identify” a leachable or extractable?
2. How do you “correlate” extractables and leachables profiles? What does the term “correlate” mean?
3. How do you optimize extractables methods? What are “asymptotic” levels?
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Introduction to Recommendation Specifics
1. Component Selection – Fran DeGrazio
2. Controlled Extraction Studies – Tom Feinberg
3. Leachables Studies and Routine Extractables Testing – Diane Paskiet
4. Analytical Evaluation Threshold – Dan Norwood
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Final Points
• The “Best Practice” recommendations are designed to be comprehensive.
• We welcome your comments and suggestions.
• I did not personally create the issue of leachables/extractables in OINDP.