The document summarizes analytical techniques for characterizing polymeric excipients processed with hot melt extrusion (HME). It discusses using size exclusion chromatography coupled with infrared spectroscopy (SEC-IR) to analyze three case studies:
1) SoluPlus copolymer stability after HME at different temperatures and screw speeds showed compositional drifts but no degradation.
2) HPMCAS processing showed succinic acid formation above 190°C indicating degradation.
3) PEA/MAA crosslinking was observed at 190°C forming anhydrides from carboxylic acids. SEC-IR identified changes and degradation products from HME for each excipient.
Determination of the Gas-Phase Acidities of the Cysteine-Polyglycine Peptideskiran_uoh
ASMS 2008 Poster:
• The gas-phase acidities of eighteen cysteinepolyglycine
peptides were determined using
the extended kinetic method. The entropy
factor is important in these systems.
• The gas-phase acidity of the cysteine residue
increases systematically with the increase in
the length of the peptide.
• It is worth mentioning that the CGn peptides are
more acidic than the corresponding GnC
peptides.
Determination of the Gas-Phase Acidities of the Cysteine-Polyglycine Peptideskiran_uoh
ASMS 2008 Poster:
• The gas-phase acidities of eighteen cysteinepolyglycine
peptides were determined using
the extended kinetic method. The entropy
factor is important in these systems.
• The gas-phase acidity of the cysteine residue
increases systematically with the increase in
the length of the peptide.
• It is worth mentioning that the CGn peptides are
more acidic than the corresponding GnC
peptides.
This presentation by Cray Valley talks about surface treatments for optimizing dispersion of halogen-free, flame retardant minerals. It highlights water-based coatings and the reasons behind investigating fire-resistant plastics. This slideshow reveals Cray Valley's investigation into relevant surface treatments for specific mineral systems, methods to coat filler and elongating dispersion.
"Polymers in Cables" takes a close and comprehensive approach to wire and cable material enhancements. Focus areas for this study include curing performance rubber, inorganic mineral dispersion, and flow and processibility optimization.
Cray Valley's ongoing study of polymer modification is presented, in part, in this slideshow. It specifically focuses on dissecting the differentiating commodity minerals with unique surface treatments. Topics covered include dispersing technology, the effect of dispersion in CaCO3-filled PP, and the analogue in PA6.
Adding Value to Recycled Polyamides with Polyfunctional Chain ExtendersTotal Cray Valley
Cray Valley performed research to improve the mechanical properties of reprocessed recycled nylon derived from carpet using a functional additive and expand the application space of virgin grade nylon using the same chain extension mechanism.
For more information on Cray Valley, go to www.crayvalley.com
This paper will focus on Cooperative learning in science education.
Curcumin extract is subjected to 1H NMR, 13C NMR, and 2D -HSQC FT-NMR analysis for structure
the 2D NMR specra may be obtained that indicate coupling between hydrogens and carbons to which they are attached. In this case it is called heteronuclear correlation spectroscopy (HECTOR, HSQC, or C-H HECTOR).
Highly stable pt ru nanoparticles supported on three-dimensional cubic ordere...suresh899
The cost of the catalysts used in the direct methanol fuel cell
poses a challenge to its widespread use as an energy efficient and environment
friendly fuel conversion technology. In this study, two types of highly ordered
mesoporous carbon CMK-8 (I and II) with high surface area and 3-D
bicontinuous interpenetrating channels were synthesized and deposited with
PtRu nanoparticles using the sodium borohydride reduction method. The
electrocatalytic capabilities for methanol oxidation were investigated using
cyclic voltammetry and chronoamperometry, and the results were compared
with that of PtRu deposited on Vulcan XC-72 using the same preparation
method as well as with commercial PtRu/C (E-TEK) catalyst. Pt Ru/CMK-8-I synthesized by the method developed in this work revealed an
outstanding specific mass activity (487.9 mA/mg) and superior stability
compared with the other supports, thus substantiating its potential to reduce
the costs of DMFC catalysts.
This presentation by Cray Valley talks about surface treatments for optimizing dispersion of halogen-free, flame retardant minerals. It highlights water-based coatings and the reasons behind investigating fire-resistant plastics. This slideshow reveals Cray Valley's investigation into relevant surface treatments for specific mineral systems, methods to coat filler and elongating dispersion.
"Polymers in Cables" takes a close and comprehensive approach to wire and cable material enhancements. Focus areas for this study include curing performance rubber, inorganic mineral dispersion, and flow and processibility optimization.
Cray Valley's ongoing study of polymer modification is presented, in part, in this slideshow. It specifically focuses on dissecting the differentiating commodity minerals with unique surface treatments. Topics covered include dispersing technology, the effect of dispersion in CaCO3-filled PP, and the analogue in PA6.
Adding Value to Recycled Polyamides with Polyfunctional Chain ExtendersTotal Cray Valley
Cray Valley performed research to improve the mechanical properties of reprocessed recycled nylon derived from carpet using a functional additive and expand the application space of virgin grade nylon using the same chain extension mechanism.
For more information on Cray Valley, go to www.crayvalley.com
This paper will focus on Cooperative learning in science education.
Curcumin extract is subjected to 1H NMR, 13C NMR, and 2D -HSQC FT-NMR analysis for structure
the 2D NMR specra may be obtained that indicate coupling between hydrogens and carbons to which they are attached. In this case it is called heteronuclear correlation spectroscopy (HECTOR, HSQC, or C-H HECTOR).
Highly stable pt ru nanoparticles supported on three-dimensional cubic ordere...suresh899
The cost of the catalysts used in the direct methanol fuel cell
poses a challenge to its widespread use as an energy efficient and environment
friendly fuel conversion technology. In this study, two types of highly ordered
mesoporous carbon CMK-8 (I and II) with high surface area and 3-D
bicontinuous interpenetrating channels were synthesized and deposited with
PtRu nanoparticles using the sodium borohydride reduction method. The
electrocatalytic capabilities for methanol oxidation were investigated using
cyclic voltammetry and chronoamperometry, and the results were compared
with that of PtRu deposited on Vulcan XC-72 using the same preparation
method as well as with commercial PtRu/C (E-TEK) catalyst. Pt Ru/CMK-8-I synthesized by the method developed in this work revealed an
outstanding specific mass activity (487.9 mA/mg) and superior stability
compared with the other supports, thus substantiating its potential to reduce
the costs of DMFC catalysts.
LC-IR Applications In Polymer Related Industriesmzhou45
LC-IR Application Overview for Polymer Related Industries with Many Case Studies: characterize copolymer compositions across MWD and de-formulate complex polymer mixtures
New LC-IR Technique To Characterize Polymeric Excipients In Pharmaceutical Fo...mzhou45
GPC-IR combined technique to characterize polymeric excipients for lot-to-lot variations and degradation/stability from thermal processing in drug formulations
Deformulating Complex Polymer Mixtures By GPC-IR Technologymzhou45
GPC-IR to de-formulate complex polymer mixtures such as adhesives, coatingg, inks, additives to identify polymer components and find their specific raw material suppliers by IR database search. The presentation was given at American Coating Conference 2012 on May 7 in Indy.
Plant hormones are of vital importance for normal functioning of plants that coordinate the growth and development of plants with response to the environment. Plant hormones are difficult to analyze because they occur in very low amounts in plant extracts which are very rich in interfering substances, especially secondary metabolites. To cope with this problem the plant extract must undergo several purification steps using unrelated separation mechanisms in order to increase orthogonality and purification efficiency (Dobrev et al., 2005). High performance liquid chromatography and Gas liquid chromatography are frequently used in the purification and quantification of plant hormones like Abscisic acid, Indole acetic acid etc.
A method for estimation of Abscisic acid in Arabidopsis thaliana includes an extraction of plant tissues with acetone/water/acetic acid (80:19:1, v/v), evaporation of the extracts and finally injection into the liquid chromatography-electrospray ionization tandem mass spectrometry (LC–ESI–MS–MS) system in multiple reaction monitoring (MRM) mode (Carbonell and Jáuregui, 2005).
A novel metabolic profiling approach to the analysis of acidic phytohormones and other metabolites based on a simplistic preparation scheme and analysis by chemical ionization-gas chromatography/mass spectrometry has also been developed (Schmelz et al., 2004). But Current metabolomic approaches are able to quantify highly abundant primary and secondary metabolites but do not perform well at detecting trace levels of phytohormones.
Separate profiling methods, with comparatively more elaborate sample preparation procedures, are now making phytohormone profiles accessible using trace analysis chemical ionization GC/MS techniques. Using LC/MS detection, a significant phytohormone profiling advance was recently achieved (Chiwocha et al. 2003).
Similar to AAPS2011 Oral--Analytical Techniques To Characterize Excipient Stability & Degradation From Hot Melt Extrusion (9)
AAPS2011 Oral--Analytical Techniques To Characterize Excipient Stability & Degradation From Hot Melt Extrusion
1. AAPS 2011 Meeting 10/26/2011
Analytical Techniques to Characterize the Stability
and Degradation of Polymeric Excipients
from Hot Melt Extrusion Processing
Ming Zhou, PhD
Director of Applications Engineering
Spectra Analysis Instruments, Inc.
Contact: ZhouM@Spectra-Analysis.com
Tel. 508-281-6276 1
2. OUTLINE
Overview: Analytical Techniques to Characterize Polymers
Introduce SEC-IR Hyphenated Technique
SEC-IR to Characterize Excipient Degradation from HME:
SoluPlus, HPMCAS, PEA/MAA
Summary
Note: Size Exclusion Chromatography (SEC) = Gel Permeation Chromatography (GPC)
2
3. Analytical Techniques to
Characterize Homopolymers Poly(A)
Absorption
High MW Low MW Molar Mass
Polymer MWD Affects Many Application Properties
4. Analytical Techniques to
Characterize Homopolymers Poly(A)
SEC / GPC
(FFF)
Absorption
High MW Low MW Molar Mass
Composition Analysis Thermal Analysis
NMR DSC or DMA: Tg, Tm
IR, ATR-IR, Raman TGA: Weight Loss w/ Temp.
NIR Pyrolysis GC-MS: Volatile Degradant
MS (MW<10K), difficult to ionize
UV-Vis
5. Analytical Techniques to Characterize
Copolymers Poly(A-B)
Absorbance
A/B composition
molar mass
ratio
high MW low MW
polymer chains
comonomer A
comonomer B
5
6. Analytical Techniques to Characterize
Copolymers Poly(A-B): Compositions
Composition
Analysis:
NMR
FTIR, Raman
Absorbance
A/B composition
molar mass
ratio NIR
Bulk Average
high MW low MW
polymer chains
comonomer A
comonomer B
6
7. Analytical Techniques to Characterize
Copolymers Poly(A-B): Compositions
Absorbance SEC / GPC
A/B composition
molar mass
ratio
Bulk Average
high MW low MW SEC / GPC
ElutionTime
Composition
Analysis:
IR
polymer chains
NMR comonomer A
MS
HPLC comonomer B
7
8. Hyphenated Techniques to
Characterize Copolymers Poly(A-B)
Absorbance SEC / GPC
A/B composition
molar mass
ratio
high MW low MW SEC Time
Hyphenated (Coupling) Techniques
Composition SEC-IR
Analysis: LC—NMR: Fractionation (Batching)
IR
polymer chains
LC-MS: for Low MW Portion
NMR 2D LC: HPLC x SEC; IPC x SEC
comonomer A
MS
HPLC TGA-IR: Volatilecomonomer B
Degradant
TGA + GC-MS: Volatile Degradant 8
9. SEC-IR to Characterize Compositional
Variations of Copolymers Poly(A-B)
IR Spectra
A
B
Absorbance
A/B composition
molar mass
ratio
high MW low MW SEC Time
polymer chains
comonomer A
comonomer B
9
12. ZnSe Sample Disk
Rotate at tunable speed
10-0.3 mm/min
The yellow ZnSe disk is under
vacuum without moisture or
CO2 interference
Disk Temp: -140C ~ 100C
Transmission IR analysis is
done on the solid deposit.
Unattended overnight runs
Re-usable after solvent
cleaning
12
13. Features of LC-IR System
Real-Time On-line Detection
Microgram Sensitivity
All HPLC Solvents, Gradients & Volatile Buffers
• e.g. Water, ACN, Methanol, THF, DMSO …
All SEC/GPC Solvents: e.g. THF, DMF, Chloroform, TCB, HFIP
High Quality Solid Phase Transmission IR Spectra
Fully Automated Operation: No More Manual Fractionation
Multi-Sample Processing: 10 Hr ZnSe Disk Time
15. OUTLINE
Overview: Analytical Techniques to Characterize Polymers
Introduce SEC-IR Hyphenated Technique
SEC-IR to Characterize Excipient Degradation from HME:
SoluPlus, HPMCAS, PEA/MAA
Summary
Note: Size Exclusion Chromatography (SEC) = Gel Permeation Chromatography (GPC)
15
16. Case #1: SoluPlus Copolymer
Stability from HME Processing
Sample # Temp. Screw Sample Solution Degradant Polymer
(C) Speed Color in DMF Formed Changed ?
(rpm) (~2%) ?
R Not White Clear
(Ref.) Processed Powder Solution
A 120 125 Off Clear ? ?
White Solution
B 120 250 Off Clear ? ?
White Solution
C 180 125 Yellowish Clear ? ?
White Solution
D 180 250 Yellowish Clear ? ?
White Solution 16
17. SoluPlus Sample Preparation &
SEC-IR Operating Conditions
Sample Preparation:
• SoluPlus excipient was extruded at different temperatures: 120oC &
180oC and at different extrusion speed 125 rpm & 250 rpm.
• 0.20 g SoluPlus solid samples were dissolved in 10 ml DMF in ~1.5
hr and filtered with 0.45 mm PTFE syringe filter before GPC injection
SEC Chromatography: Agilent® 1200
• SEC Column Temperature: Ambient
• Solvent: DMF at 1.0 ml/min
• Column: Jordi Gel DVB Mixed Bed– 250 x 10 mm
• Sample Injections: 25 ml at ~2% weight / volume DMF
IR Detection
• DiscovIR-LC® solvent-removing direct-deposition solid phase FTIR
• Cyclone Temperature: 225oC
• Condenser Temperature: -5oC
• ZnSe Disk Temperature: 55oC
18. IR Band Identifications
of SoluPlus Copolymer
HO
Group VAc VCap Note
PEG VCap
O
O
N C=O 1738 cm-1 1642 cm-1 Peak Ratios for
Compositional
l
O m
Drifts w/ MWD
n
O Acetyl 1244 cm-1 Internal Ratio
O Check vs.
O Peak 1738
VAc
CH3 1374 cm-1
HO
Peak 1642 cm-1 from VCap comonomer Methyl Acetyl
1374 1244
Peak 1738 cm-1 from VAc comonomer
19. Acetyl Internal Ratio Check
Almost Flat across MWD for Sample B
1738/1244 Peak Height Ratios
All from VAc Group
Polymer IR Spectrum at Red Marker
Polymer IR Spectrum at Blue Marker
20. SEC-IR Band Chromatogram & IR
Spectra of SoluPlus Ref. Sample
Band Chromatogram at 1642 cm-1
1642
Polymer IR Spectrum at Red Marker
1738
1642
Polymer IR Spectrum at Blue Marker 1738 VCap
VAc
21. SoluPlus Ref. Compositional Drifts w/
Elution Time (MWD) by IR Peak Ratios
Comonomer VAc/VCap Ratio ~ Carbonyl Peak 1738/1642 Height Ratio:
Abs(VAc) / Abs(VCap) = (k1*b*MVAc) / (k2*b*MVCap) = k (MVAc / MVCap)
Peak 1738/1642 Height Ratio
Peak 1738/1642 Height Ratio
1642
IR Polymer IR Spectrum at Red Marker
Spectrum at Red Cursor (Elution Time)
1738
1642
IR Spectrum atIR Spectrum at Blue Marker
Polymer Blue Cursor (Peak Chromatogram) 1738 VCap
VAc
(Molecular Weight Distribution)
22. SoluPlus Stability: VAc/VCap Ratios
Drift Similarly w/ MWD after HME
R – Green Unprocessed Reference
A – Black Processed at 120C @ 125rpm
B – Blue Processed at 120C @ 250rpm
C – Brown Processed at 180C @ 125rpm
D – Violet Processed at 180C @ 250rpm
22
24. SEC-IR Matrix Study Summary:
SoluPlus Stability in HME Processing
Sample # Temp. Screw Sample Solution Degradant Polymer
(C) Speed Color in DMF Formed Changed ?
(rpm) (~2%) ?
R Not White Clear Not VAc/VCap
(Ref.) Processed Powder Solution Detected Ratio Drift
w/ MWD
A 120 125 Off Clear Not Same
White Solution Detected VAc/VCap
Ratio Drift
B 120 250 Off Clear Not Same
White Solution Detected VAc/VCap
Ratio Drift
C 180 125 Yellowish Clear Not Same
White Solution Detected VAc/VCap
Ratio Drift
D 180 250 Yellowish Clear Not Same
White Solution Detected VAc/VCap
24
Ratio Drift
25. Case #2: HPMCAS Stability &
Degradation from HME
Sample # Extrusion Sample Sample Degradant Polymer
Temp. Color in THF Formed ? Change?
(~0.5%)
Ref. Not White Clear None None
Processed Powder Solution
A 180 C Yellowish Clear
Powder Solution
B 200 C Yellowish Some ? ?
Powder Residue
C 220 C Brownish Some ? ?
Powder Residue
25
26. SEC-IR Band Chromatogram & IR
Spectra of HPMCAS Sample (220oC)
Band Chromatogram at 1720 cm-1
Low MW Degradant
at 14.6’
Polymer
Polymer IR Spectrum at Red Marker
Polymer IR Spectrum at Blue Marker
28. SEC-IR Band Chromatogram to
Identify Degradant & Additive
Band Chromatogram at 1670 cm-1 Sample C
for HPMCAS & Additive & Degradant (HME @220oC)
Polymer
Degradant IR Spectrum at 14.6 Min. (Red Marker)
Succinic Acid
Additive IR Spectrum at 14.1 Min. (Blue Marker)
Baseline Not Corrected
29. IR Spectra Overlay of HPMCAS,
Additive & Degradant from Sample C
1670cm-1
Baselines Not Corrected
Succinic Acid at 14.65 Min
Additive at 14.1 Min
HPMCAS at 11.2 Min
Additive-Specific Peak
30. SEC-IR Band Chromatogram of
Additive only for HPMCAS Ref. Sample
Band Chromatogram at 3360 cm-1 No Degradant
for Additive Only at 14.1 Min. (Succinic Acid)
Additive IR Spectrum at 14.6 Min. (Red Marker)
No Succinic Acid
Additive IR Spectrum at 14.1 Min. (Blue Marker)
31. Degradant Level Comparison of
HPMCAS Samples after HME
Band Chromatograms at 1670 cm-1
Sample C: Violet (220C)
Sample B: Brown (200C)
Sample A: Aqua (180C)
Sample R: Blue (Ref.)
Degradant
at 14.6 Min.
Normalized to Additive Level
Additive
at 14.1 Min.
32. Degradant Level Increases with
Higher HME Processing Temp.
Succinic Acid Formation with Hot Melt ExtrusionTemperature
5
Succinic Acid Normalized Peak Height
4.5
4
3.5
3
2.5
2
1.5
1
0.5
0
0 50 100 150 200 250
Process Temperarure (C) ~190oC
Samples: Ref. A B C
33. HPMCAS Matrix Study Summary:
Degradation & Stability from HME
Sample # Extrusion Sample Sample Degradant Polymer
Temp. Color in THF Formed Change
(~0.5%)
Ref. Not White Clear None None
Processed Powder Solution
A 180 C Yellowish Clear Little None
Powder Solution Succinic
Acid
B 200 C Yellowish Some Succinic
Powder Residue Acid
C 220 C Brownish Some Succinic Higher
Powder Residue Accid OH/C=O
Ratio
33
34. Case #3: PEA/MAA Samples
from Hot Melt Extrusion Process
Sample # Extrusion Screw Sample Sample Degradant Polymer
Temp. Speed Color in THF Formed Changed
(~0.5%) ? ?
S0 Not White Clear
Processed Solution
S1 130 C 250 rpm Off Clear
White Solution
S2 160 C 250 rpm Off Clear
White Solution
S3 190 C 250 rpm Brownish Some ? ?
Residue
Note: Samples S1-S3 contain 20% plasticizer TEC to assist extrusion process. 34
35. IR Spectra of PEA/MAA Samples
at Polymer MWD Center (ET ~9.4’)
S0 – Green Ref COOEt
S1 – Violet 130C 1735
S2 – Blue 160C
S3 – Black 190C
COOH
1705
NCE?
1805 cm-1
CO-OH
35
36. PEA/MAA Crosslinked to Anhydride
from COOH at Higher HME Temp
COOEt
1735 S0 – Green Ref
S1 – Violet 130C
S2 – Blue 160C
COOH S3 – Black 190C
1705
NCE?
1805 cm-1
36
37. PEA/MAA Matrix Study Summary:
Degradation & Stability from HME
Sample # Extrusion Screw Sample Sample Degradant Polymer
Temp. Speed Color in THF Formed Change
(~0.5%)
S0 Not White Clear None None
Processed Solution
S1 130 C 250 rpm Off Clear Trace
White Solution Anhydrides
S2 160 C 250 rpm Off Clear Anhydrides Acid/Ester
White Solution Ratio
Decreased
S3 190 C 250 rpm Brownish Some Anhydrides Acid/Ester
Residue Ratio
Decreased
37
38. Common Polymeric Excipients
for Hot Melt Extrusion by SEC-IR
?
HOOC-CH2-CH2-C=O
HPMCAS ~ 190C COCH3
PEA/MAA ~ 160C
HO
O
O
N
l
O m
n
Copovidone > 200C O
O
O
H - (OCH2CH2 )n - OH SoluPlus > 200C
PEG HO
Excipient Combinations with Plasticizers and Additives
38
40. Summary
SEC-IR Maps out Polymer Compositions across MWD (Sizes) for
Copolymers and Formulated Polymer Mixtures
SEC-IR Useful to Characterize Excipient Stability/Degradation
from HME Processing: SoluPlus, HPMCAS, PEA/MAA
Detected Degradants (Low MW)
Analyzed Polymer Compositional / Structural Changes:
• Cross-Linking (New Chemical Entity) & Functional Group Changes
Define Safe Processing Windows / QbD to Validate Excipient Stability
40
41. Summary: SEC-IR Applications
Profile Polymer Compositions = f (Sizes)
IR Spectra B A
A/B Ratio
Absorbance
High MW Low MW SEC
Elution
Time
Map out Copolymer Compositions (A/B Ratio) across MWD (Sizes)
41
42. Summary: SEC-IR Applications
Profile Polymer Compositions = f (Sizes)
IR Spectra B A
A/B Ratio
Absorbance
High MW Low MW SEC
Elution
Time
Map out Copolymer Compositions (A/B Ratio) across MWD (Sizes)
Study Lot-to-Lot Variations
42
43. Summary: SEC-IR Applications
Profile Polymer Compositions = f (Sizes)
IR Spectra B A
A/B Ratio
Absorbance
High MW Low MW SEC
Elution
Time
Map out Copolymer Compositions (A/B Ratio) across MWD (Sizes)
Study Supplier-to-Supplier Variations (2nd Source)
43
44. Summary: SEC-IR Applications
Profile Polymer Compositions = f (Sizes)
IR Spectra B A
A/B Ratio
Absorbance
High MW Low MW SEC
Elution
Time
Map out Copolymer Compositions (A/B Ratio) across MWD (Sizes)
Study Lot-to-Lot or Supplier-to-Supplier Variations
Characterize Polymer Degradation from Processing:
Loss of functional group A (Reduced A/B)
44
45. Summary: SEC-IR Applications
Profile Polymer Compositions = f (Sizes)
Cross Linking
IR Spectra B A
A/B Ratio
Absorbance
High MW Low MW SEC
Elution
Time
Map out Copolymer Compositions (A/B Ratio) across MWD (Sizes)
Study Lot-to-Lot or Supplier-to-Supplier Variations
Characterize Polymer Degradation from Processing:
Loss of functional group A (Reduced A/B)
45
Cross-linking ( Higher MW)
46. Summary: SEC-IR Applications
Profile Polymer Compositions = f (Sizes)
Break Down
IR Spectra B A
A/B Ratio
Absorbance
High MW Low MW SEC
Elution
Time
Map out Copolymer Compositions (A/B Ratio) across MWD (Sizes)
Study Lot-to-Lot or Supplier-to-Supplier Variations
Characterize Polymer Degradation from Processing:
Loss of functional group (Reduced A/B)
46
Cross-linking ( Higher MW)
Break down ( Lower MW) & Detect low MW degradant
47. Summary: SEC-IR Applications
Profile Polymer Compositions = f (Sizes)
Cross Linking Break Down
IR Spectra B A
A/B Ratio
Absorbance
High MW Low MW SEC
Elution
Time
Map out Copolymer Compositions (A/B Ratio) across MWD (Sizes)
Study Lot-to-Lot or Supplier-to-Supplier Variations
Characterize Polymer Degradation from Processing:
Loss of functional group (Reduced A/B)
47
Cross-linking ( Higher MW)
Break down ( Lower MW) & Detect low MW degradant
De-Formulate Complex Polymer Mixtures
48. Summary: SEC-IR Characterization
of Excipient Copolymers Poly(A-B)
IR Spectra B A
A/B Ratio
Absorbance
High MW Low MW SEC
Elution
Time
Map out copolymer compositions across MWD (sizes)
Lot-to-lot or supplier-to-supplier variations
Degradation from processing:
Loss of functional group
Cross-linking
Break down, Low MW degradant
Validate Excipient Stability: To define safe processing window (QbD)
49. LC-IR Applications for Excipient
Analysis in Drug Formulations
Excipient Formulation Develop. Formulated Drugs
Manufacturing Drug Manufacturing Shelf Life Stability
• Process Control • Incoming QC-Variations • Stressed
• Lot-to-lot Variations • Excipient Functionality Degradation
• CoA • Formulation Development
• QbD • De-Formulate
• Novel Excipient Excipient Blends
R&D • Process Degradation
(Hot Melt Extrusion)
• Define Safe Process
Window / QbD
• Process Monitoring
• Trouble Shooting • Trouble Shooting
• Trouble-Shoot
Problem Drugs in
the Market
Users: Excipient Pharma Co. Pharma Co.
Manufacturers HME Service Providers Generic Drug Co.