from synthesis to bio-transformation: control and
TRANSCRIPT
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Prof. Marco TerreniFull Professor in Medicinal Chemistry, University of Pavia; Drug Sciences Department
President of Italian Biocatalysis Center (IBC)
EDQM (Council of Europe, Strasburg): Expert for the Commission of Certification of Suitability
From synthesis to bio-transformation: control and management of the quality of APIs
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Qualità di un principio attivo
Nuovi farmaci:EMEA (ICH Guide line)
Farmaci Generici:ICH Guide lineFarmacopea
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Relevance of the impurity content in APIs
Isolation could be impossible:levels should be reduced by improving purification processes
Identification by:GC or HPLC-MS analysis (hypothesis of the possible structure/s)Chemical synthesis (structure correlation)
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General monograph “Substances for pharmaceutical use” (2034)
General monograph “Substances for pharmaceutical use” (2034)
• To be applied to “all” substances for pharma use• Describes the general requirements with regards
quality and purity• In particular when a specific monograph is not in
compliance with its principles • Most sections are applicable to fermentation
products and products obtained by bio-processes
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General monograph 2034 (cont)General monograph 2034 (cont)
• the Related substances Section does not apply to fermentation products, but gives principles to be applied, namely:– Qualify and specify main impurities– As much as possible identify impurities and
specify them– Set a limit of « other impurities »
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General monograph (2034)General monograph (2034)
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PeptidesPeptides
• Generally used at low daily dose• Many potential related substances: isomers, results
of failures in sequences, cleavages or coupling• Requirements for related substances included in
the general monograph 2034 from 1/07/2009:
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Qualification of Impurities
Time consumingDelayed registration and commercialization of the product
The level of any impurity present in a new drug substance that has been adequately tested in safety and/or clinical studies would be considered qualified.
Impurities in known active ingredient can be qualified comparing the impurity profile with existing commercial products
New impurity in known active ingredient (as reported in Eur. Ph) should be adequately tested in safety and/or clinical studies for qualification.
• Genotoxicity studies (point mutation, chromosomal aberration)• General toxicity studies (one species, usually 14 to 90 days)• Other specific toxicity endpoints, as appropriate
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PROBLEMS OF THE CHEMICAL SYNTHESIS
•Use of toxic solvents and reagents polluting waste
•Time-consuming andmulti-step procedures
sometimes•Formation of by-products•residual solvents low yields
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i. Reaction in aqueous medium (low environmental impact);ii. Use of no toxic and no pollutants reagents;iii. Soft reaction conditions;iv. Avoiding of protection and deprotection steps;v. Reduction of the purification steps;vi. High purity of the final product.
Use of enzymes in the synthesis of active ingredients
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MICRO-ORGANISM
ISOLATION OF THE ENZYME
Single step reaction
Solid catalyst
Crude extractFermentation broth
•Lipases•Esterases•Amidases•Glycosidases•Reductases•Oxidases•Transferases
Purification
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ENZYME PREPARATION
Free soluble enzymes
Insoluble preparations of pure or almost pure enzymes
Enzymes immobilized on solid supports
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Isolated Enzymes
•Fermentation Broth•Crude extract
•Purified Enzymes•Solid or Immobilised Enzymes
Mixture of several proteins
Fermentation-like•Residuals arising from micro-organism• Complex downstream
Potential Residual Proteins
No use of animal origins raw material in the production of the enzyme
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REACTORS WITH ULTRAFILTRATION
SOLUBLE ENZYMES CAN BE RE-USED
ALL INACTIVATION MECHANISMS
ARE POSSIBLE:aggregationproteolysisinteraction with interfaces
SS
S
S
S
S
S
P
P
P
P
P
P
P PP
S
FREE SOLUBLE ENZYMES
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1 2 3 4 5 61 2 3 4 5 6
94,00094,00067,00067,000
43,00043,000
30,00030,000
20,10020,100
14,40014,400
1 2 3 4 5 61 2 3 4 5 6
94,00094,00067,00067,000
43,00043,000
30,00030,000
20,10020,100
14,40014,400
1 2 3 4 5 61 2 3 4 5 6
94,00094,00067,00067,000
43,00043,000
30,00030,000
20,10020,100
14,40014,400
FREE ENZYME ARE OFTEN COMPLEX MIXTURES
•Contamination by different proteins•Side reactions catalyzed by different enzymes•Other contaminants contained in the crude extract
SDS-PAGE RML
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OPTIMIZATION OF THE BIO-CATALYST:SOLID AND INSOLUBLE ENZYMES
OPTIMIZED ENZYMESOPTIMIZED ENZYMES
Re-use of the biocatalystStabilisation of the biocatalystSimplification of the downstream
Improved stabilityImproved yieldsNo contamination
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ENZYME DERIVATIVES WITHOUT SUPPORT
All the solid is enzymeNo cost of the supportmechanical stabilityRigidificaction of the enzyme ?Micro-environment ?
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Stabilization of Multimeric Enzymes
Problem
Dissociation of the subunitsin drastic reaction conditions
High pHHigh temperature
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POSSIBILITIES
CLECs
Pure crystalline enzyme:
requirement of extremepure enzyme
Stabilization ofMultimeric enzymes
CLEAs
Crude enzyme:
Co-aggregation of enzyms
Aggregation of enzyme and polymer
Stabilization of multimeric enzymes
Crosslinked Enzyme Crystals Crosslinked Enzyme Aggregates
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CLEAs
Preparation of CLEAs
cross linking agent
+ Floculating agent:
PEGSalts, solvents
Cao L. et al; Org. Lett (2000) 2: 1361-64
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IMMOBILIZATION OF ENZYMES ON PREEXISTING SUPPORTS
covalent multi-point attachment
reversible immobilization by adsorption
cost of the supportresidues after inactivation of the catalyst (covalent
derivatives)possible release of protein in the reaction medium
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-OOC
-OOC
++
HN
HN
CH2
CH2
Extreme temperatureand presence of co-solvents
HYDROPHOBICADSORPTION
Extreme temperatureand pH
IONICADSORPTION
No release;Special case:
multimeric enzymes
COVALENTATTACHMENT
Release of protein from immobilised enzymes
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Optimisation of the catalystOptimisation of the catalyst
Design of theenzyme derivative
Avoid the Release of proteinin the reaction medium
Avoid the Release of proteinin the reaction medium
•Stability•Catalytic properties
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IMMOBILIZATION BY ADSORPTION
Easy protocols of immobilization
The support can be re-usedafter enzyme inactivation
Reduction of residues
Possible product contamination with the enzyme
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pH = 8
Enzyme
Enzyme
HN
OH
OH2N
Covalent Immobilisation on Epoxidic Supports
No residual protein
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Dissociation of the subunits:•Low stability of the enzyme•Residual protein in the final product
Dissociation of the subunits:•Low stability of the enzyme•Residual protein in the final product
Special case: Multimeric enzymes
Covalent immobilisation
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Acylase from A. turbidans
Enzymatic synthesis of Ampicillin
40 % of methanol;Phosphate buffer atlow concentration;
Dissociation of the subunits:Low stability of the enzymeIn the synthetic conditions
Dissociation of the subunits:Low stability of the enzymeIn the synthetic conditions
Enz. Microb. Technol. 25 (1999) 336-343
O
H2NNH2
N
S
COOH
COOCH3
O
HN
O
NH2
N
S
COOH
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AN INTEGRATED APPROACH TO THESTABILIZATION OF MULTIMERIC ENZYMES
2. SUBUNIT CROSSLINKING WHIT POLYFUNCTIONAL MOLECULES
CHO
Polyaldehydes
CHO CHO
CHOCHOCHO
1. MULTI - SUBUNIT COVALENT IMMOBILIZATION
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0
25
50
75
100
0 10 20 30 40
TIME, (hours)
Resi
dual
act
ivity
, (%
)
Stability of the enzyme derivatives
Crosslinked derivative
Free enzyme
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Immobilised EnzymeImmobilised Enzyme
Suitability of the downstream process
Knowledge of the catalyst engineering
Control of residual proteins
Test for residual proteins in thefinal product
Test for release of proteins in thereaction condition
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1. Fermentation Processes
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General monograph « Products of fermentation » (1468)
General monograph « Products of fermentation » (1468)
• Scope:– « Indirect » gene products obtained by fermentation
• Out of the scope:– Vaccines, products from continuous cell lines, of
animal/human origin– Direct gene products– Semi-synthetic products, biocatalytic process
• Provides general requirements for manufacture of fermentation products. Compliance mandatory for these products
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FERMENTATION
Advantages•One step reaction: synthesis of complex molecules
• Low costs
Disadvantages•Complex mixtures
•Contaminants with different structures•Residuals arising from micro-organisms
• Complex downstream•Complex separation and analytical procedure for control of
impurities
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Product of fermentation Complex structures
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Simple compounds, normally prepared by chemical synthesis, are more and more prepared by fermentation.For example:
•Aminoacids•Nucleosides and nucleotides•Vitamins
Control of the quality is depending from the process used.
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RequirementsRequirements• Source and history of the producer micro-organism• Characterisation, stability, of the producer micro-
organism• Detailed description of fermentation, incl materials,
preparation of media, downstream processing• In-process controls at all stages• Purity of the final substance: impurity profile and
specification
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Impurity profileImpurity profile
• Impurities (3.2.S.3)– Describe all potential related substances
(sometimes complex), focus on actual impurities– Address residual solvents according to European
guidelines– Discuss particular impurities arising from
fermentation: residues of substrates, cells residues, proteins,…
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Limits for related substancesLimits for related substances
• Set limits according to the monograph• Set limits for the other known impurities
– Qualify impurity profile by comparison with products already on the market, or tox data
– In line with levels found in batches• Set limits for unknown impurities + total
impurities
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Limits for residual solventsLimits for residual solvents
• According to ICH and CHMP guidelines on Residual solvents
• Show absence of the solvents used during purification
• Set limits and propose methods for solvents used during purification
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Other impuritiesOther impurities
• Demonstrate that there are no residues from fermentation
• Proteins: not a concern for oral use (a lime proposed), to be addressed if parenteral use (absence should be demonstrated)
• DNA• The Ph. Eur provides general methods which
can be used
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downstream:Elimination of residuals from micro-organism
•Extraction with organic solventsallows complete elimination of residuals. Presence of residual indicate a not well separation of phases.•Crystallization in organic solventMost adequate for residuals elimination•Ultra filtrationResiduals of low molecular weight proteins and peptides•Chromatographic columnsComplete elimination of protein is ensured depending from the chromatographic conditions
Problems for high water soluble products:•Peptides•Amino acids•Oligosaccharides•Nucleosides and nucleotides
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Evaluation of residuals arising from the micro-organism
Nucleic acids•Absorbance tests•RT-PCR or PCR
Proteins•Colorimetric tests: Bradford, Lowry or other according to the Monograph for Assay of Total Protein 2.5.33 (01/2008:20533)•Electrophoresis
•Absence of residuals from the microorganism should be demonstratedduring process validation•Product for injection should be carefully controlled
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Example of fermentation product:L-serine
Isolation from fermentation broth:• Filtration of biomass• Anionic and cationic exchange resinsPurification:• Ultrafiltration of water solution (cut-off m.w.>6000)• Crystallization from waterPossible impurities:Aminoacids. Analysis performed with A.A. analyzer (each NMT 0.2%;
total NMT 1.0%).Absence of protein demonstrated by Bradfford assay (colorimetric: LOD
1ug/mL)
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Example of Enzymatic bioprocess: L-serine
Enzyme Isolation from fermentation broth:• Filtration of biomass• Solution is directly used without purification of the enzymePurification:• Ionic exchange colums• Crystallization from organic solvent/water solution• Ultrafiltration of water solution (cut-off m.w.>5000)• Crystallization from waterPossible impurities:Glicine (starting material) and other A.A. Analysis performed with A.A. analyzer (each
NMT 0.5%; total NMT 1.0%).Absence of protein demonstrated by adsorbance at 650 nm (LOD 40 ppm)
Glicine L-SerineEnzyme
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Is a Complex mixture of products. Problems related to:.•Identification•Quality
Example of fermentation product: Teicoplanine….a long story
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Teicoplanine
Composition of the “Complex”and related substances are strictly dependent from:•Microorganism•Control of the Fermentation process•Raw material used for fermentation process
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Teicoplanine New ProducerJapan Pharcopoea (JP)
Commercial Medicinal product (Tangosit) and the new Teicoplanine APImeet specification for JP
Csilla FranK; Controllo della qualità di un prodotto di fermentazione: aspetti tecnici e regolatoriThesis “Master in Discipline Regolatorie 2008”; University of Pavia; Pavia; Italy
JPSpecification
TeicoBatch A
TeicoBatch B
TeicoBatch C
TA2 GroupNLT 80%
95.24 94.04 90.50
TA3 GroupNMT 15%
3.71 4.45 8.28
OtherNMT 5%
1.05 1.51 1.22
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Teicoplanine: satisfaction of EP Specification
EPSpecification
TeicoBatch A
Teico Batch B
TeicoBatch C
TA2-1 GroupNMT 20%
9.3 8.3 7.7
TA2-2 GroupNMT 35-55%
47.7 47.7 48.7
TA2-3 GroupNMT 20%
8.2 7.5 7.0
TA2-4 GroupNMT 20%
14.8 14.1 13.5
TA2-5 GroupNMT 20%
6.7 7.1 7.1
EPSpecification
TeicoBatch A
Teico Batch B
TeicoBatch C
TA2-1 GroupNMT 20%
10.65 6.32 8.62
TA2-2 GroupNMT 35-55%
59.54 56.54 55.01
TA2-3 GroupNMT 20%
9.04 10.69 8.95
TA2-4 GroupNMT 20%
4.27 7.51 5.05
TA2-5 GroupNMT 20%
2.79 5.26 3.57
Modulation of fermentation conditionSelection of the ingredient used during fermentation
Out of Specification Conform with the Specification
Csilla FranK; Controllo della qualità di un prodotto di fermentazione: aspetti tecnici e regolatoriThesis “Master in Discipline Regolatorie 2008”; University of Pavia; Pavia; Italy
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According to Guide line on setting specification for related impurities in antibiotics
Proposed limits for Active Substances manufactured by fermentation: Fanmily of compoundReporting threshold: 0.10%Identification threshold 0.15%Qualification threshold unknown 0.15%Qualification threshold related 0.50%Identification at least by HPLC-MS
Limit for impurities in Teicoplanin?
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Any other peak in the chromatogram should be identified and confirmed to have a teicoplanin-like structure.
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1. Evaluationof the complex according to the EMA guide line.2, Compariosion of the new product with EP-CRS and commercial product
EVALUATION OF TEICOPLANINE QUALITY
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3. Confirmation of Teicoplanine-like impurities by HPLC-MS analysis4. Specification for impurities >0.5% specified by RRT5. Revision of the EP monograph under evaluation accordingly