monash institute of pharmaceutical sciences sheep as a clinically relevant model to assess the...
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Monash Institute of Pharmaceutical Sciences
Sheep as a clinically relevant model to assess the pharmacokinetics of colistin and colistin methanesulfonate after pulmonary and intravenous administration
Dr Tri-Hung NguyenDrug Delivery to the Lung Conference Edinburgh, December 2012
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• Increasing prevalence in hospital environments
• Product of antimicrobial misuse
• Sources of MDR lung infections
• Klebsiella pneumoniae
• Acinetobacter baumanii
• Pseudomonas aeruginosa
• Opportunistic infections
• Prevalent amongst immunocompromised patients
• Cystic fibrosis
• Critically ill
Multiple drug resistant Gram negative infections
Soon et al. Antimicrob Agents Chemother 2006
0 5 µm
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Antimicrobial Development
Clatworthy et al., Nat Chem Biol 2007.
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Antimicrobial Resistance
Clatworthy et al., Nat Chem Biol 2007.
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Declining numbers of new antimicrobial agents
1983-87 1988-92 1993-97 1998-2002 2003-07 2008-12
To
tal n
um
be
r o
f n
ew
ag
ents
0
2
4
6
8
10
12
14
16
18
Adapted from Spellberg et al. Clin Infect Dis 2011 Antimicrobials with activity against Gram-negatives
EMEA 2009
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Antimicrobial Resistance
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Colistin (Polymyxin E)
O
OO
O
O
O
O
O
O
OHO
HO
O
NH
HN
HNH
N
HN
NH
HN
NH
HN
HN
NH
NH2
NH2
NH2
NH2
NH2 R6
R1
1 L-Dab
2 L-Thr
3 L-Dab
4 L-Dab
5 L-Dab
7 L-Leu
8 L-Dab
9 L-Dab
10 L-Thr
Colistin R6 = D-LeuPolymyxin B R6 = D-PheColistin A & polymyxin B1 R1 = 6-methyloctanoic acidColistin B & polymyxin B2 R1 = 6-methylheptanoic acid
• Cationic polypeptide antimicrobial
• First used in the 1950’s and 1960’s
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Colistin (Polymyxin E)
• Cationic polypeptide antimicrobial
• First used in the 1950’s and 1960’s
• Amphiphilic molecule
• Hydrophilic peptide ring
O
OO
O
O
O
O
O
O
OHO
HO
O
NH
HN
HNH
N
HN
NH
HN
NH
HN
HN
NH
NH2
NH2
NH2
NH2
NH2 R6
R1
1 L-Dab
2 L-Thr
3 L-Dab
4 L-Dab
5 L-Dab
7 L-Leu
8 L-Dab
9 L-Dab
10 L-Thr
Colistin R6 = D-LeuPolymyxin B R6 = D-PheColistin A & polymyxin B1 R1 = 6-methyloctanoic acidColistin B & polymyxin B2 R1 = 6-methylheptanoic acid
Peptide Ring
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Colistin (Polymyxin E)
• Cationic polypeptide antimicrobial
• First used in the 1950’s and 1960’s
• Amphiphilic molecule
• Hydrophilic peptide ring
• Hydrophobic tail
O
OO
O
O
O
O
O
O
OHO
HO
O
NH
HN
HNH
N
HN
NH
HN
NH
HN
HN
NH
NH2
NH2
NH2
NH2
NH2 R6
R1
1 L-Dab
2 L-Thr
3 L-Dab
4 L-Dab
5 L-Dab
7 L-Leu
8 L-Dab
9 L-Dab
10 L-Thr
Colistin R6 = D-LeuPolymyxin B R6 = D-PheColistin A & polymyxin B1 R1 = 6-methyloctanoic acidColistin B & polymyxin B2 R1 = 6-methylheptanoic acid
Hydrophobic tail
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Colistin (Polymyxin E)
• Cationic polypeptide antimicrobial
• First used in the 1950’s and 1960’s
• Amphiphilic molecule
• Hydrophilic peptide ring
• Hydrophobic tail
• Mode of action
• Positively charged amino groups
• Interaction with bacterial cell membrane
O
OO
O
O
O
O
O
O
OHO
HO
O
NH
HN
HNH
N
HN
NH
HN
NH
HN
HN
NH
NH2
NH2
NH2
NH2
NH2 R6
R1
1 L-Dab
2 L-Thr
3 L-Dab
4 L-Dab
5 L-Dab
7 L-Leu
8 L-Dab
9 L-Dab
10 L-Thr
Colistin R6 = D-LeuPolymyxin B R6 = D-PheColistin A & polymyxin B1 R1 = 6-methyloctanoic acidColistin B & polymyxin B2 R1 = 6-methylheptanoic acid
Positively charged
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Colistin and colistin methanesulfonate (CMS)
• Colistin
• Nephrotoxicity and neurotoxicity on high systemic exposure
• Superseded by newly developed antibiotics
• Bronchoconstriction when inhaled
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Colistin and colistin methansulfonate (CMS)
• Colistin
• Nephro- and neurotoxicity on high systemic exposure
• Superseded by newly developed antibiotics
• Bronchoconstriction on inhaled use
• Inactive prodrug
• Colistin methanesulfonate (CMS)
• Amines replaced with methylene sulfonic acid moieties
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Clinical use of colistin and CMS
•Colistin currently used in clinical practice
•Inconsistencies with doses administered
•Need to refine dosing regimens
• Improve efficacy
• Prevent resistance
•Potential toxicity at high dose limits dose excursions
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Clinical use of colistin and CMS
•Colistin currently used in clinical practice
•Inconsistencies with doses administered
•Need to refine dosing regimens
• Improve efficacy
• Prevent resistance
•Potential toxicity at high dose limits dose excursions
Can a pre-clinical model be used to assess targeted delivery of antibiotics and inform clinical practice?
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In vivo lung models Mouse Rat Guinea-pig Dog Sheep Human
Body mass (kg) 0.02-0.04 0.25-0.35 0.4 10-15 45 70-80
Nose/mouth breathers
Nose Nose Nose Nose/mouth Nose/mouth Nose/mouth
Trachea-bronchial branching pattern
Monopodial Monopodial Monopodial Monopodial Dichotomous Irregularly
dichotomous
Lung mass (g) 0.12 1.5 - 100 250-1000 1000
Lung volume (mL) 0.74 8.6 13 736 2800 4341
Lung Lobation5 lobes
left lung (1) and right lung (4)
Left lung is not divided
-6 lobes
left lung (2) and right lung (4)
6 lobes left lung (2) and
right lung (4)
5 lobes left lung (2) and
right lung (3)
Alveoli diameter (μm)
47 70 65 126 150-300 200-400
Tidal volume (ml) 0.15-0.18 0.87-2.08 1.72 – 1.75
11.4 – 16.6
180 – 405 400 – 616
Respiratory rate (breaths/min)
163 85 90 23 15 – 40 12
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Hypothesis
Sheep are a suitable preclinical model to assess the localised delivery of an antimicrobial to the lung
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• 6 merino sheep
• Four way randomised crossover study
• Surgical cannulation
• Jugular vein: IV administration
• Carotid artery: Blood collection
• IV administration
• 2.5 mg/kg or equivalent
• Colistin (sulfate salt)
• CMS (sodium salt)
• IV infusion at 1 mL/min
• Blood and broncho-alveolar lavage (BAL) fluid sampled up to 24 hr after administration
In-vivo studies
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Pulmonary administration of colistin and CMS
• Conducted in conscious sheep
• Endotracheal tube directed via nostril into the trachea
• Colistin and CMS solution nebulised over 25 min
• Blood sampled up to 24 hr after administration
• BAL fluid collected from lung sections
• 1, 4 and 24 hr after administration
• Colistin and CMS plasma analysed via HPLC
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Data analysis
• Non-compartmental analysis
• Population modeling (S-ADAPT and SADAPT-TRAN software/MC-PEM algorithm)
• Takes into account the true biological variability between sheep
• Enables prediction of concentration vs. time profiles at other dosage regimens
• Supports translation from sheep into humans and allometric scaling
• The PK model can be combined with a pharmacodynamic model to predict antibacterial effects
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IV colistin pharmacokinetics
• IV colistin sulfate
• Fits 3 compartment model
• Decrease in plasma concentrations over time
Time (h)
0 2 4 6 8 10
Dru
g plasma concentration (m
g/L)
0.1
1
10
100
1000Colistin sulfate
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IV CMS pharmacokinetics
• IV CMS
• Fits 3 compartment model
• Decrease in plasma concentrations over time
• Similar elimination phase
• Colistin conversion from CMS
• Increased concentration over time
• No colistin/CMS concentrations were detected in epithelial lung fluid (ELF)
Time (h)
0 2 4 6 8 10
Dru
g plasma concentration (m
g/L)
0.1
1
10
100
1000CMSColistin from CMS
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IV colistin and CMS pharmacokinetics
• IV colistin sulfate and CMS
• Fits 3 compartment model
• Decrease in plasma concentrations over time
• Similar elimination phase
• Colistin conversion from CMS
• Increased concentration over time
• No colistin/CMS concentrations were detected in epithelial lung fluid (ELF)
Time (h)
0 2 4 6 8 10
Dru
g plasma concentration (m
g/L)
0.1
1
10
100
1000Colistin sulfateCMSColistin from CMS
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IV colistin from CMS pharmacokinetics
Pharmacokinetic Parameter
Colistin from CMS Sheep
Colistin from CMS Human
Colistin from CMS Rat
AUC (mg/L x h) 23.9 ± 7.5
t1/2 (h) 9.1 ± 6.1
Tmax (h) 3.1 ± 0.55
Cmax (mg/L) 2.6 ± 0.4
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IV colistin from CMS pharmacokinetics
Pharmacokinetic Parameter
Colistin from CMS Sheep
Colistin from CMS Humans
Colistin from CMS Rats
AUC (mg/L x h) 23.9 ± 7.5
t1/2 (h) 9.1 ± 6.1 *5.9-14.4
Tmax (h) 3.1 ± 0.55
Cmax (mg/L) 2.6 ± 0.4
٭ Imberti et al. Chest (2010) Garonzik et al. Antimicrob. Agents Chemother. (2011) Plachouras et al. Antimicrob. Agents Chemother. (2009)
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IV colistin from CMS pharmacokinetics
Pharmacokinetic Parameter
Colistin from CMS Sheep
Colistin from CMS Humans
Colistin from CMS Rats
AUC (mg/L x h) 23.9 ± 7.5
t1/2 (h) 9.1 ± 6.1 *5.9-14.4 #0.4-1.2
Tmax (h) 3.1 ± 0.55
Cmax (mg/L) 2.6 ± 0.4
٭ Imberti et al. Chest (2010) Garonzik et al. Antimicrob. Agents Chemother. (2011) Plachouras et al. Antimicrob. Agents Chemother. (2009)
# Marchand et al. J. Antimicrob. Chemother. (2010) Li et al. Antimicrob Agents Chemother (2003) Li et al. Antimicrob Agents Chemother (2004)
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Population PK model: IV clearance
Pharmacokinetic Parameter
ColistinSheep
Colistin Humans
ColistinRats
Clearance (L/h) 1.3 *1.1 #0.1
* Reed et al. J. Clin Pharmacol. (2002) # Li et al. J. Antimicrob. Chemother. (2003)
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Local delivery of colistin and CMS to the lung
• Epithelial lung fluid concentration
• Colistin and CMS concentration decreased over time
• Colistin from CMS increased then decreased
• Conversion from CMS
• No detectable colistin concentration measured in plasma
• Consistent with human data
• < 0.14mg/L*
• Colistin binding to tissues?Time (h)
1 4 24
Colistin/C
MS
Concentration (m
g/L)
10
100
1000
10000Colistin Sulfate CMSColistin from CMS
* Ratjen et al. J. Antimicrob. Chemother. (2006) Jensen et al. J. Antimicrob. Chemother. (1987)
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Local delivery of colistin and CMS to the lung
• Epithelial lung fluid concentration
• Colistin and CMS concentration decreased over time
• Colistin from CMS increased then decreased
• Conversion from CMS
• No detectable colistin concentration measured in plasma
• Consistent with human data
• < 0.14 mg/L*
• Colistin binding to tissues?
* Ratjen et al. J. Antimicrob. Chemother. (2006) Jensen et al. J. Antimicrob. Chemother. (1987)
Marchand et al. Antimicrob. Agents Chemother (2010)
Systemic plasma concentrations measured in rats
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Population PK model: Lung delivery
PUL colistin dose
Colistin in
ELFColistin in lung
tissues
Colistin clearance (4.6 mL/h)
distributionColistin in absorption
compartment
absorption
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Population PK model: Lung delivery
PUL CMS dose
PUL colistin dose
CMS in ELF
Colistin in
ELF
CMS in lung tissues
Colistin in lung tissues
Metabolism to colistin
Colistin clearance (4.6 mL/h)
distribution
Metabolism to colistin
distribution
CMS in absorption compartment
Colistin in absorption
compartment
absorption
absorption
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Summary• Sheep were examined as a clinically relevant model to assess the PK of the
antimicrobial colistin and CMS
• Decreases in CMS plasma concentrations after IV administration corresponded to an increase in formed colistin
• No colistin or CMS detected in ELF after IV administration
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Summary• Sheep were examined as a clinically relevant model to assess the PK of the
antimicrobial colistin and CMS
• Decreases in CMS plasma concentrations after IV administration corresponded to an increase in formed colistin
• No colistin or CMS detected in ELF after IV administration
• CMS concentrations decreased in ELF over 24 h with increasing colistin concentrations after pulmonary administration
• No colistin or CMS detected in plasma
• Correlates to clinical data
• Population PK modeling indicated that CMS was distributed and metabolised in ELF and lung tissue after pulmonary administration
• Sheep have been demonstrated to be a clinically relevant model to evaluate the PK of antimicrobials administered to the lung.
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Acknowledgments
Monash Institute of Pharmaceutical Sciences
Dr Michelle McIntosh
Linh Lieu
Biotechnology Research Laboratories (Monash University)
Prof Els Meeusen
Dr Robert Bishcof
Gary Nguyen
Centre for Medicine Use and Safety (Monash University)
Dr Cornelia Landersdorfer
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Monash Institute of Pharmaceutical Sciences
Sheep as a clinically relevant model to assess the pharmacokinetics of colistin and colistin methansulfonate after pulmonary and intravenous administration
Dr Tri-Hung NguyenDrug Delivery to the Lung Conference Edinburgh, December 2012
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Population PK model: IV administration
IV CMS dose
IV colistin dose
CMS in plasma
Colistin in
plasma
CMS in slowly equilibrating
tissues
Colistin in
slowly equilibrating
tissues
Metabolism to colistin
colistin elimination
distribution
Metabolism to colistin
distribution
Metabolism to colistin
CMS in rapidly equilibrating
tissues
Colistin in
rapidly equilibrating
tissues
CMS elimination
distribution
distribution
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Population PK model: IV clearance
Parameter Colistin from CMS Colistin
Clearance (L/h) 1.32 0.784
Central volume of distribution (L) 0.50 0.32
Peripheral volume of distribution (Fast equilibrating, L)
7.45 3.25
Peripheral volume of distribution (Slow equilibrating, L)
92.9 59.1
Conversion of CMS to colistin in central and fast equilibrating peripheral compartment (h-1)
0.05