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Academic-industrial collaborations in
  respiratory drug delivery & development
Dr. Sally-Ann Cryan, School of Pharmacy, RCSI
Gobal BioPharma Summit, Dublin Oct 31st 2012




                                                1
Pharmaceutical Development
                 Drug Compound
                (Discovery Phase)




                 Pharmaceutical
                  Development




                Medicinal product
                (patient-end user)
Translational pharmaceutics for respiratory therapeutics
• Basic biomedical research
   – Molecular pharmaceutics
   – In vitro cell culture studies
   – HTS for respiratory cells
• Applied clinical research
   – Translational pharmaceutics
       • formulation of “therapeutic” cargoes
   – In vivo pre-clinical studies
       • delivery, toxicology, pharmacokinetics
• Industrial research/commercialisation
   – Product development
   – Device development
   – Particle delivery platforms
Inhaled medicines

•   Ancient civilisations, current smokers
    and drug abusers know the efficacy of
    inhaled drugs
•   Route harnessed by scientists and
    physicians for therapeutic drug delivery
•   Convenient and targeted drug delivery
    directly to site of action for respiratory
    conditions
•   Growing interest in its use for systemic
    delivery and delivery of
    biopharmaceuticals
Currently inhaled medicines
•   Beta-2 agonists e.g. salbutamol, terbutaline
•   Corticosteroids e.g. budesonide, beclomethasone
•   Anti-cholinergics e.g ipratropium bromide
•   Anti-inflammatory e.g. comoglycate
•   Mucolytics e.g. DNase, N-acetylcysteine
•   Antibiotics e.g. tobramycin, pentamidine
•   Anti-proteases e.g. Alpha-1-antitrypsin

     – Applications
         • Asthma
         • COPD
         • Cystic fibrosis
Respiratory drug delivery market
• Worldwide market for prescription respiratory medicines is now more
  than $64B
• Predicted global pulmonary drug delivery technologies market of up to
  $44B by 2016
    – significant portion of growth supported by technological advances in
      biomaterials-based delivery systems
• Eamples of locally acting molecules for inhaled delivery:
    – Secretory leukocyte inhibitor (rSLPI), Interferon-γ, Cyclosporin A, Gene
      therapies (pDNA, siRNA/shRNA, miRNA)
• Examples of systemically acting molecules for inhaled delivery
    – Insulin, FSH, Calcitonin, hGH, Interferon-α, Heparin
Challenges from Delivery & Development Perspective

• Pharmaceutical & Regulatory issues
   – Inefficient delivery
   – Expense of biomolecules
– Instability
   – Lack of licensed excipients
                                 • Biopharmaceutical issues
   – Inadequate screening tools
                                    – Instability & rapid clearance in vivo
   – Multi-drug regimens
                                    – Poor site-specific targeting
                                    – Cell-type specific targeting
                                    – Poor intracellular delivery
                                    – Toxicology and immunogenicity
                                    – Poor IVIVIC
Meeting the Challenges & Harnessing Opportunities:
              academic-industrial collaboration

Drivers/Needs:
•Therapeutic biomolecules
•Device applications
•Pre-clinical testing
•Personnel training
Example 1: Therapeutic Biomolecule
Secretory Leukocyte Protease Inhibitor (rSLPI) therapy
rSLPI therapeutic properties:
•   Endogenous cationic protein with antiprotease activity
•   Anti-oxidant; Anti-bacterial; Anti-viral activity; Anti-inflammatory
Barriers to inhaled rSLPI therapy:
•   Delivery                                                     Strategy:
                                                                 rSLPI-loaded liposomes
     – Degradation during aerosolisation & processing            Enhance in vivo stability
     – Poor lung distribution                                    Improve lung retention &
                                                                 sustained release
•   Pharmacokinetic: short half-life                             Decrease toxicity
     – Proteolytic: degradation by cathepsins                    Protect during aerosolisation
•   Toxicological
                                                                              Epithelial cells
     – High doses may cause lung Irritation
Collaborators: Prof. Gerry McElvaney & Dr. Catherine Greene (Beaumont & RCSI), Prof. Clifford
Taggart (QUB), Amgen
Particle Engineering for Respiratory Drug Delivery
Particle Engineering for Respiratory Drug Delivery:
          Approved Biomaterials/Excipients
Improving rSLPI pharmacokinetics
                                                                   Intracellular rSLPI




rSLPI Transport in vitro: Calu-3 monolayer



                                       rSLPI transport in vivo: guinea pig asthma model
                                                           Gibbons et al., Pharm Res 2011
Effect of liposome encapsulation of rSLPI on targeting




   DOPC Liposomes   DOPS Liposomes    Gibbons et al Pharm Res 2011
Development of a liposome-rSLPI dry powder for inhalation




 Manufacturing an inhalable
 powder of DOPS-rSLPI

Gibbons et al
                              Stability of liquid & dry powder formulations of rSLPI-DOPS
AAPSPharmSciTech 2010
Meeting the Challenges & Harnessing Opportunities:
              academic-industrial collaboration

Drivers/Needs:
•Therapeutic biomolecules
•Device applications
•Pre-clinical testing
•Personnel training
Aerogen™-IDDN collaborations
  Projects Focus:
  • Project 1 Optimising performance:
  Investigation of fluid physicochemical properties on
     Aerogen™ performance

  • Project 2 Expanding applications:
  Effect of nebulisation on the stability of a range of
     therapeutic biomolecule

  • Project 3 Added value:
  Development of convergent device-drug particle
    platforms
Project 1 Optimising performance
Investigation of fluid physicochemical properties on Aeroneb® performance
Project 2 Expanding applications:
Effect of nebulisation on the stability of a range of therapeutic biomolecule




 RP-HPLC of calcitonin pre- and post
 nebulisation




                                        SEC of calcitonin pre- and post-nebulisation
Project 3: Added Value
Nebulised Nanoparticles for
Pulmonary siRNA Delivery
convergent device-nanoparticle
system




                          Kelly et al 2012 RNAi for
                          Respiratory disease
Development of Nebulised Nanoparticles for
Pulmonary siRNA Delivery
                         Undifferentiated Calu-3                                Differentiated Calu-3
                                  Pre-neb %KD
                    80
                                  Post-neb %KD
      % Knockdown




                    60


                    40


                    20


                    0




                                                       5
                                                      1
                               5




                                                     =
                               1




                                                                                                               Pre-neb %KD

                                                   /P
                              =
                            /P




                                                  N
                                                                                                               Post-Neb %KD
                           N




                                                                           60
                                                  G
                           I




                                                             % Knockdown
                                              E
                          E




                                              P
                         P




                                            I-
                                           E
                                          P




                                                                           40



                                                                           20



                                                                           0




                                                                                                           5
                                                                                                           1
                                                                                          5




                                                                                                          =
                                                                                         1




                                                                                                        /P
                                                                                        =
                                                                                     /P




                                                                                                       N
                                                                                    N




                                                                                                     G
                                                                                    I




                                                                                                   E
                                                                                   E




                                                                                                 P
                                                                                  P




                                                                                               I-
                                                                                               E
                                                                                              P
                                                           Hibbitts et al unpublished
Meeting the Challenges & Harnessing Opportunities:
              academic-industrial collaboration

Drivers/Needs:
•Therapeutic biomolecules
•Device applications
•Pre-clinical testing
•Personnel training
Example 3: Pre-clinical testing
                Screening of Nanomedicines in Respiratory Cells




Oglesby et al. Respiratory Research 2010,
                 11:148




  Collaborators: Prof. Gerry McElvaney & Dr. Catherine Greene (Beaumont & RCSI)
Example 3: Pre-clinical testing
                             B
      Screening of Nanomedicines in Respiratory Cells
Control                    PEI-miRNA, N:P 10:1       Blue=nucleus

                                                     Green=cytoskeleton

                                                     Red=nanomedicines




Chitosan-miRNA, N:P 50:1   Chitosan-TPP-miRNA, N:P
                           200:1
Secreening of “Smart” Biomaterials/Excipients

Example: Star-shaped polypeptide carriers




       Heise Group, DCU
Advanced tools for Respiratory Drug Development:
                                 3D Modelling of the Airway
                                                    Potential Applications:
                                                       – Co-culture models
                                                       – Toxicity & immunogenciity (including
                                                         nanotoxicology)
                                                       – Disease models
  Taken from Klein et al., Toxicol in Vitro, 2011
                                                       – Regeneration




                                                                        Calu-3 cultures after 14 days
    Collagen-Gag Scaffold (O’Brien lab)

Collaborators: RCSI TERG & Dr. Shirley O’Dea & Prof. Noel G McElvaney
Opportunities in the Irish Context
• Interdisciplinary research to maximise impact: clinical, biomedical,
  pharmaceutical, engineering
• Academic-industrial partnership: convergent technologies
• Biomedical respiratory research
    – In vitro and in vivo studies
    – Range of therapeutic cargoes emerging
        • Small molecules and biomolecules
• Indigenous translational & commercial respiratory research platforms
  & know-how
    – To realise full clinical & commercial potential of basic research
    – Drug product development & IP
              – Biomaterials
              – Device
              – Screening tools
Acknowledgements
Research Team:        Respiratory Collaborators:
•Dr. Aileen Gibbons   •Dr. Marc Devocelle & Dr. James Barlow (RCSI)
•Dr. Awadh Yadav      •Prof. NG McElvaney & Dr. Catherine Greene (Beaumont& RCSI)
•Dr. Ciaran Lawlor    •Prof. Joe Keane & Dr. Mary O’Sullivan (SJH)
•Dr. Ciara Kelly      •Dr. Brian Robertson & Dr. Robert Endres (Imperial College London)
•Dr. Joanne Ramsey    •Dr. Shirley O’Dea (NUIM)
•Alan Hibbitts        •Prof. Clifford Taggart (QUB)
•Cian O’Leary         •Prof. Anthony Hickey (UNC-Chapel Hil)
•Paul McKiernan       •Dr Ronan MacLoughlin (Aerogen)
                      •Prof. Fergal O’Brien (RCSI)

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Dr Sally-Ann Cryan, Senior Lecturer in Pharmaceuticals, RCSI

  • 1. Academic-industrial collaborations in respiratory drug delivery & development Dr. Sally-Ann Cryan, School of Pharmacy, RCSI Gobal BioPharma Summit, Dublin Oct 31st 2012 1
  • 2. Pharmaceutical Development  Drug Compound (Discovery Phase)  Pharmaceutical Development Medicinal product (patient-end user)
  • 3. Translational pharmaceutics for respiratory therapeutics • Basic biomedical research – Molecular pharmaceutics – In vitro cell culture studies – HTS for respiratory cells • Applied clinical research – Translational pharmaceutics • formulation of “therapeutic” cargoes – In vivo pre-clinical studies • delivery, toxicology, pharmacokinetics • Industrial research/commercialisation – Product development – Device development – Particle delivery platforms
  • 4. Inhaled medicines • Ancient civilisations, current smokers and drug abusers know the efficacy of inhaled drugs • Route harnessed by scientists and physicians for therapeutic drug delivery • Convenient and targeted drug delivery directly to site of action for respiratory conditions • Growing interest in its use for systemic delivery and delivery of biopharmaceuticals
  • 5. Currently inhaled medicines • Beta-2 agonists e.g. salbutamol, terbutaline • Corticosteroids e.g. budesonide, beclomethasone • Anti-cholinergics e.g ipratropium bromide • Anti-inflammatory e.g. comoglycate • Mucolytics e.g. DNase, N-acetylcysteine • Antibiotics e.g. tobramycin, pentamidine • Anti-proteases e.g. Alpha-1-antitrypsin – Applications • Asthma • COPD • Cystic fibrosis
  • 6. Respiratory drug delivery market • Worldwide market for prescription respiratory medicines is now more than $64B • Predicted global pulmonary drug delivery technologies market of up to $44B by 2016 – significant portion of growth supported by technological advances in biomaterials-based delivery systems • Eamples of locally acting molecules for inhaled delivery: – Secretory leukocyte inhibitor (rSLPI), Interferon-γ, Cyclosporin A, Gene therapies (pDNA, siRNA/shRNA, miRNA) • Examples of systemically acting molecules for inhaled delivery – Insulin, FSH, Calcitonin, hGH, Interferon-α, Heparin
  • 7. Challenges from Delivery & Development Perspective • Pharmaceutical & Regulatory issues – Inefficient delivery – Expense of biomolecules – Instability – Lack of licensed excipients • Biopharmaceutical issues – Inadequate screening tools – Instability & rapid clearance in vivo – Multi-drug regimens – Poor site-specific targeting – Cell-type specific targeting – Poor intracellular delivery – Toxicology and immunogenicity – Poor IVIVIC
  • 8. Meeting the Challenges & Harnessing Opportunities: academic-industrial collaboration Drivers/Needs: •Therapeutic biomolecules •Device applications •Pre-clinical testing •Personnel training
  • 9. Example 1: Therapeutic Biomolecule Secretory Leukocyte Protease Inhibitor (rSLPI) therapy rSLPI therapeutic properties: • Endogenous cationic protein with antiprotease activity • Anti-oxidant; Anti-bacterial; Anti-viral activity; Anti-inflammatory Barriers to inhaled rSLPI therapy: • Delivery Strategy: rSLPI-loaded liposomes – Degradation during aerosolisation & processing Enhance in vivo stability – Poor lung distribution Improve lung retention & sustained release • Pharmacokinetic: short half-life Decrease toxicity – Proteolytic: degradation by cathepsins Protect during aerosolisation • Toxicological Epithelial cells – High doses may cause lung Irritation Collaborators: Prof. Gerry McElvaney & Dr. Catherine Greene (Beaumont & RCSI), Prof. Clifford Taggart (QUB), Amgen
  • 10. Particle Engineering for Respiratory Drug Delivery
  • 11. Particle Engineering for Respiratory Drug Delivery: Approved Biomaterials/Excipients
  • 12. Improving rSLPI pharmacokinetics Intracellular rSLPI rSLPI Transport in vitro: Calu-3 monolayer rSLPI transport in vivo: guinea pig asthma model Gibbons et al., Pharm Res 2011
  • 13. Effect of liposome encapsulation of rSLPI on targeting DOPC Liposomes DOPS Liposomes Gibbons et al Pharm Res 2011
  • 14. Development of a liposome-rSLPI dry powder for inhalation Manufacturing an inhalable powder of DOPS-rSLPI Gibbons et al Stability of liquid & dry powder formulations of rSLPI-DOPS AAPSPharmSciTech 2010
  • 15. Meeting the Challenges & Harnessing Opportunities: academic-industrial collaboration Drivers/Needs: •Therapeutic biomolecules •Device applications •Pre-clinical testing •Personnel training
  • 16. Aerogen™-IDDN collaborations Projects Focus: • Project 1 Optimising performance: Investigation of fluid physicochemical properties on Aerogen™ performance • Project 2 Expanding applications: Effect of nebulisation on the stability of a range of therapeutic biomolecule • Project 3 Added value: Development of convergent device-drug particle platforms
  • 17. Project 1 Optimising performance Investigation of fluid physicochemical properties on Aeroneb® performance
  • 18. Project 2 Expanding applications: Effect of nebulisation on the stability of a range of therapeutic biomolecule RP-HPLC of calcitonin pre- and post nebulisation SEC of calcitonin pre- and post-nebulisation
  • 19. Project 3: Added Value Nebulised Nanoparticles for Pulmonary siRNA Delivery convergent device-nanoparticle system Kelly et al 2012 RNAi for Respiratory disease
  • 20. Development of Nebulised Nanoparticles for Pulmonary siRNA Delivery Undifferentiated Calu-3 Differentiated Calu-3 Pre-neb %KD 80 Post-neb %KD % Knockdown 60 40 20 0 5 1 5 = 1 Pre-neb %KD /P = /P N Post-Neb %KD N 60 G I % Knockdown E E P P I- E P 40 20 0 5 1 5 = 1 /P = /P N N G I E E P P I- E P Hibbitts et al unpublished
  • 21. Meeting the Challenges & Harnessing Opportunities: academic-industrial collaboration Drivers/Needs: •Therapeutic biomolecules •Device applications •Pre-clinical testing •Personnel training
  • 22. Example 3: Pre-clinical testing Screening of Nanomedicines in Respiratory Cells Oglesby et al. Respiratory Research 2010, 11:148 Collaborators: Prof. Gerry McElvaney & Dr. Catherine Greene (Beaumont & RCSI)
  • 23. Example 3: Pre-clinical testing B Screening of Nanomedicines in Respiratory Cells Control PEI-miRNA, N:P 10:1 Blue=nucleus Green=cytoskeleton Red=nanomedicines Chitosan-miRNA, N:P 50:1 Chitosan-TPP-miRNA, N:P 200:1
  • 24. Secreening of “Smart” Biomaterials/Excipients Example: Star-shaped polypeptide carriers Heise Group, DCU
  • 25. Advanced tools for Respiratory Drug Development: 3D Modelling of the Airway Potential Applications: – Co-culture models – Toxicity & immunogenciity (including nanotoxicology) – Disease models Taken from Klein et al., Toxicol in Vitro, 2011 – Regeneration Calu-3 cultures after 14 days Collagen-Gag Scaffold (O’Brien lab) Collaborators: RCSI TERG & Dr. Shirley O’Dea & Prof. Noel G McElvaney
  • 26. Opportunities in the Irish Context • Interdisciplinary research to maximise impact: clinical, biomedical, pharmaceutical, engineering • Academic-industrial partnership: convergent technologies • Biomedical respiratory research – In vitro and in vivo studies – Range of therapeutic cargoes emerging • Small molecules and biomolecules • Indigenous translational & commercial respiratory research platforms & know-how – To realise full clinical & commercial potential of basic research – Drug product development & IP – Biomaterials – Device – Screening tools
  • 27. Acknowledgements Research Team: Respiratory Collaborators: •Dr. Aileen Gibbons •Dr. Marc Devocelle & Dr. James Barlow (RCSI) •Dr. Awadh Yadav •Prof. NG McElvaney & Dr. Catherine Greene (Beaumont& RCSI) •Dr. Ciaran Lawlor •Prof. Joe Keane & Dr. Mary O’Sullivan (SJH) •Dr. Ciara Kelly •Dr. Brian Robertson & Dr. Robert Endres (Imperial College London) •Dr. Joanne Ramsey •Dr. Shirley O’Dea (NUIM) •Alan Hibbitts •Prof. Clifford Taggart (QUB) •Cian O’Leary •Prof. Anthony Hickey (UNC-Chapel Hil) •Paul McKiernan •Dr Ronan MacLoughlin (Aerogen) •Prof. Fergal O’Brien (RCSI)