4.8 Article

Topical delivery of low-cost protein drug candidates made in chloroplasts for biofilm disruption and uptake by oral epithelial cells

期刊

BIOMATERIALS
卷 105, 期 -, 页码 156-166

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2016.07.042

关键词

Antimicrobial peptide; Drug delivery; Plant biopharmaceuticals; Dental caries; Therapeutic enzymes

资金

  1. Bill and Melinda Gates Foundation [OPP1031406]
  2. NIH [R01 HL107904, R01 HL109442, R01 EY 024564, R01 DE18023, R01 DE025220]
  3. Bill and Melinda Gates Foundation [OPP1031406] Funding Source: Bill and Melinda Gates Foundation

向作者/读者索取更多资源

Protein drugs (PD) are minimally utilized in dental medicine due to high cost and invasive surgical delivery. There is limited clinical advancement in disrupting virulent oral biofilms, despite their high prevalence in causing dental caries. Poor efficacy of antimicrobials following topical treatments or to penetrate and disrupt formed biofilms is a major challenge. We report an exciting low-cost approach using plant-made antimicrobial peptides (PMAMPs) retrocyclin or protegrin with complex secondary structures (cyclic/hairpin) for topical use to control biofilms. The PMAMPs rapidly killed the pathogen Streptococcus mutans and impaired biofilm formation following a single topical application of tooth mimetic surface. Furthermore, we developed a synergistic approach using PMAMPs combined with matrix-degrading enzymes to facilitate their access into biofilms and kill the embedded bacteria. In addition, we identified a novel role for PMAMPs in delivering drugs to periodontal and gingival cells, 13 48 folds more efficiently than any other tested cell penetrating peptides. Therefore, PDs fused with protegrin expressed in plant cells could potentially play a dual role in delivering therapeutic proteins to gum tissues while killing pathogenic bacteria when delivered as topical oral formulations or in chewing gums. Recent FDA approval of plant-produced PDs augurs well for clinical advancement of this novel concept. (C) 2016 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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