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Foam Drying and Foam Freeze Drying Process Loss and Stability
Reinhard Vehring
Associate Director, Solid Dosage FormsMedImmune Inc.
319 North Bernardo Ave, Mountain View, CA 94043
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Outline
Introduction to Vacuum Foam Drying− History− Process− Dosage form properties
Stability and Process Loss
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Foam Drying of Milk in 1917
Foam drying is an established technique in the food industryKey features were recognized early − Concentration step− Foaming− Drying on drum or belt− Fast reconstitution
Concentrator
Whipper
Drying Drum
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Vacuum Foam Drying in the Food Industry
“Puff-drying” was established for food products in the 40’s
Department of Agriculture (Eastern Utilization Research and Development Division)developed vacuum foam drying of whole milk in the 50’s and 60’s
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Preserving Biologicals by Vacuum Foam Drying
Douglas I. Annear stabilized various bacteria by vacuum foam drying on freeze dried peptone plugs in the 50’s.
Commercialized in the 90’s (Universal Drying Technology, Victor Bronshtein; Quadrant Healthcare, Bruce Roser) Now VitriLife®; Avant Immunotherapeutics
Annear, D. I.: (1954) Nature 174, 359; (1956) Journal of Hygiene 54, 487;(1966) Nature 211, 761; (1970) Journal of Hygiene 68, 457.
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Vacuum Foam Drying Steps
PreconditioningBubble formation (boiling)Foam formation Foam desiccation / foam aging
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Bubble FormationPrecondition to set viscosity and surface tension of solutionDrop pressure below saturation pressure of the solutionHeterogeneous bubble nucleationBubble rising and inflation
Common problems− Violent boiling / splattering− Inconsistent onset of bubble
nucleation
Suggested solutions− Mixing− Chamber rotation− Seed crystals− Ultrasound− Entrained gases
latenever
+33 ms +66 ms
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Foam Formation
Bubble inflation is arrested by increasing membrane viscosityMembranes and foam cells rupture and collapse repeatedly until foam is stabilized.
Process depends on− P, T− Container geometry− Surface tension− Viscosity− Bubble nucleation and growth
rate
viscosity
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Foam Aging
Foam ages by draining and coarsening
Foam aging slows down because of − Desiccation → increase in Tg (Vacuum Foam Drying)− Evaporative cooling → freezing (Vacuum Foam Freeze
Drying)
+ 0.5 s + 1 s + 5 s + 10 s
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Foam Desiccation
Foam desiccated under collapse conditions (Drying temperature above glass transition temperature)Results in low specific surface area
VFFD Sucrose
Specific Surface Area: 0.06 m2/g
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Foam Structure
Foam can be modeled as non-porous, thin membranesSpecific surface area lower than lyo-cakeInhomogeneous structure Control of membrane thickness is important
50 µm
tA
ρ2ˆ =
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Sucrose Water State Diagram
0.0 0.2 0.4 0.6 0.8 1.0-150
-100
-50
0
50
100dry T
g
Tem
pera
ture
, °C
Sucrose Mass Fraction
Tg', C
g'
Te
glass
rubber
solution
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Drying Process Comparison
0.0 0.2 0.4 0.6 0.8 1.0-60
-40
-20
0
20
40
60
Tem
pera
ture
in °
C
Sucrose Mass Fraction
Start End
Freeze Drying
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Drying Process Comparison
0.0 0.2 0.4 0.6 0.8 1.0-60
-40
-20
0
20
40
60
Tem
pera
ture
in °
C
Sucrose Mass Fraction
Start End
Freeze Drying
Freeze FoamDrying
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Drying Process Comparison
0.0 0.2 0.4 0.6 0.8 1.0-60
-40
-20
0
20
40
60
Tem
pera
ture
in °
C
Sucrose Mass Fraction
Start End
Freeze Drying
Freeze FoamDrying
Spray Drying
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Dried Foam Characteristics
Low specific surface area− Much lower than lyo-cake− Much lower than typical spray dried powder− Slow water release and uptake
Relaxed glass − Low enthalpic relaxation− Different glass properties and crystallization
propensity compared to spray dried or freeze dried glasses
Connection to stability still unclear
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Stabilization of Live Attenuated Influenza Vaccine
0 12 24 365.5
6.0
6.5
7.0
25oC 4oC
Infe
ctiv
ity in
Log
FFU
/ml
Time in Months
Foam Formulation Influenza A/Beijing CAZ021
Long-term stability during refrigerated and room temperature storage.
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Stabilization of Live Attenuated Influenza Vaccine
4oC 25oC
Slope Time to 1 Log loss Slope Time to 1
Log loss
Formulation A/Beijing
-0.003+/-0.002 > 20 y -0.017+/- 0.006 > 4 y
FormulationA/Sydney
-0.005+/-0.002 > 15 y -0.020+/-0.006 > 4 y
FormulationB/Harbin
-0.009+/-0.002 > 9 y -0.023+/-0.005 > 3 y
Excellent long term stability for different influenza vaccines
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Stabilization of a Bacterium
0 8 16 24 32 40 48 563
4
5
6
7
8
9
-0.03+/-0.007
-0.006+/-0.003
Stability at 4°C
Lyophilized Vacuum Freeze Foam DriedVi
abili
ty in
log 10
CFU
/ml
Time in Weeks
0 8 16 24 32 40 48 563
4
5
6
7
8
9 Stability at 15°C
-0.03+/-0.006
-0.05+/-0.005
Lyophilized Vacuum Freeze Foam Dried
Viab
ility
in
log 10
CFU
/ml
Time in Weeks
Identical formulations of listeria monocytogenesprocessed by lyophilization and vacuum freeze foam drying
Lyophilized dosage form has better stability and lower process loss
Stability advantage of foam drying is not universal
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Process Loss during Foam Drying
Comparatively large process loss is often observed in foam drying.
Potential loss mechanisms:
Boiling – high shear forces, cavitation.Foaming – rapid and repeated change of local environment.Freezing – repeated freeze thaw with varying freezing rates.Drying under collapse conditions– desiccation and temperature stress.
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Process Loss Tracking
0.0 0.2 0.4 0.6 0.8 1.0-60
-40
-20
0
20
40
60
Te
mpe
ratu
re in
°C
Sucrose Mass Fraction
Start
EndFoaming
Freezing- 0.1 log
- 0.4 log
- 1 log - 1.6 log
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Process Modification Reduces Loss
Identical formulations of listeria monocytogenes processed using two different vacuum freeze foam drying cyclesSignificant improvements can be achieved by modifying drying temperatures for partially desiccated foam
70 60 50 40 30 20 10 0
1.5
1.0
0.5
0.0
Loss
in V
iabi
lity
in Δ
log 10
CFU
/ml
Water Content in %
Aggressive Process Reduced Drying Temperature
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Summary
Some biologics have superior stability when processed by vacuum foam drying.The stability advantage is not universal and not well understood.Listeria monocytogenes lost viability due to a combination of desiccation and temperature stress. Foaming and freezing did not cause damage.Process loss during foam drying can be reduced by cycle optimization.Controlling foam structure is key to process control.