4.7 Article

Antibody-Functionalized MoS2 Nanosheets for Targeted Photothermal Therapy of Staphylococcus aureus Focal Infection

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fbioe.2019.00218

Keywords

targeted photothermal therapy; Staphylococcus aureus; infection; antibody; MoS2 nanosheets

Funding

  1. National Key Research and Development Program of China [2017YFA0205302]
  2. National Natural Science Foundation of China [51503101, 21475064]
  3. Program for Changjiang Scholars and Innovative Research Team in University [IRT_15R37]
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD) [YX030003]
  5. Key Research and Development Program of Jiangsu [BE2018732]
  6. Natural Science Key Fund for Colleges and Universities in Jiangsu Province [17KJA430011]

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Bacterial biofilm-related diseases cause serious hazard to public health and bring great challenge to the traditional antibiotic treatment. Photothermal therapy (PTT) has been recognized as a promising alternative solution. However, the therapeutic efficacy of PTT is often compromised by the collateral damage to normal tissues due to the lack of bacteria-targeting capability. Here, a Staphylococcus aureus (S. aureus)-targeted PTT nanoagent is prepared based on antibody (anti-protein A IgG), polydopamine (PDA), and PEG-SH (thiolated poly (ethylene glycol)) functionalized MoS2 nanosheets (MoS2@PDA-PEG/IgG NSs, MPPI NSs). The PDA was used as bio-nano interface to facilitate the covalent conjugation of antibody and PEG-SH onto the surface of MoS2 NSs via facile catechol chemistry. Targeted PTT of MPPI NSs shows excellent inactivation efficiency of larger than 4 log (>99.99%) to S. aureus both in biofilms (in vitro) and in infected tissues (in vivo) without causing damage to normal mammalian cells. By contrast, non-targeted PTT of MoS2@PDA-PEG NSs (MPP NSs) only kills S. aureus by <90% in vitro and <50% in vivo. As a result, S. aureus focal infection in mice healed much faster after PTT of MPPI NSs than that of MPP NSs. The superiority of targeted PTT may originate from the efficient accumulation and close binding of PTT agents to bacterial cells. Therefore, MPPI NSs with bacteria-targeting capability are promising photothermal agents for effective treatment of S. aureus focal infection.

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