IADR Abstract Archives

Targeted Photodynamic Therapy of Oral Bacteria Using Antibody-Conjugated Nanoparticles

Introduction: Photodynamic therapy (PDT) is excellently suited for the treatment of bacteria in oral plaque biofilms where there is easy access for the application of photosensitiser and light sources to affected areas. Recent investigations in our lab have shown that erythrosine, a xanthene dye currently used as a plaque-disclosing agent is a potent photosensitiser of oral bacteria growing both in planktonic culture and as biofilms formed in vitro.

Objectives: While targeting of biofilm bacteria and sparing of eukaryotic cells is possible through drug dosimetry, it is also preferable to target the disease-causing organisms within plaque specifically, and thus promote the maintenance of a healthy plaque. To achieve this we employed antibody-conjugated gold nanoparticles.

Methods: Gold nanoparticles were synthesised to which had been conjugated erythrosine and antibody specific to either S. mutans or L. casei. These conjugates were designated S.m.-G-Er and L.c.-G-Er respectively. The conjugates were then used for the PDT of mixed 2 species biofilm cultures of S. mutans and L. casei grown in a constant depth film fermenter. Cell killing was determined by colony counting.

Results: The results showed that specific nanoparticles caused killing of their target organism in both a light and drug-dependent manner. Up to 2 log10 of cell kill of L. casei was achieved using L.c.-G-Er and 1.5 log10 killing of S. mutans when using S.m.-G-Er. Little cross-reactivity to the non-target organism was observed with either type of nanoparticle.

Conclusion: Specific killing of target organisms was achieved using targeted nanoparticles. The use of antibody and erythrosine-labelled nanoparticles shows potential for the targeting of specific bacterial species in oral plaque biofilms.


Pan European Federation Meeting
2006 Pan European Federation Meeting (Dublin, Ireland)
Dublin, Ireland
2006
267
Scientific Groups
  • Wood, Simon  ( University of Leeds, Leeds, N/A, United Kingdom )
  • Metcalf, D.  ( University of Leeds, Leeds, N/A, United Kingdom )
  • Devine, D.  ( University of Leeds, Leeds, N/A, United Kingdom )
  • Robinson, C.  ( University of Leeds, Leeds, N/A, United Kingdom )
  • Oral Session
    Microbiology:Cariology, Materials, Infection Control
    09/14/2006