Self‐assembly multifunctional DNA tetrahedron for efficient elimination of antibiotic‐resistant bacteria
Tiantian Wu,
Yu Fu,
Shuang Guo,
Yanqiang Shi,
Yuxin Zhang,
Zhijin Fan,
Bin Yang,
Baoquan Ding,
Yuhui Liao
Affiliations
Tiantian Wu
Molecular Diagnosis and Treatment Center for Infectious Diseases, Dermatology Hospital Southern Medical University GuangzhouChina
Yu Fu
Longgang District Central Hospital of Shenzhen ShenzhenChina
Shuang Guo
Molecular Diagnosis and Treatment Center for Infectious Diseases, Dermatology Hospital Southern Medical University GuangzhouChina
Yanqiang Shi
Molecular Diagnosis and Treatment Center for Infectious Diseases, Dermatology Hospital Southern Medical University GuangzhouChina
Yuxin Zhang
Molecular Diagnosis and Treatment Center for Infectious Diseases, Dermatology Hospital Southern Medical University GuangzhouChina
Zhijin Fan
Molecular Diagnosis and Treatment Center for Infectious Diseases, Dermatology Hospital Southern Medical University GuangzhouChina
Bin Yang
Molecular Diagnosis and Treatment Center for Infectious Diseases, Dermatology Hospital Southern Medical University GuangzhouChina
Baoquan Ding
CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience National Center for Nanoscience and Technology BeijingChina
Yuhui Liao
Molecular Diagnosis and Treatment Center for Infectious Diseases, Dermatology Hospital Southern Medical University GuangzhouChina
Abstract Antibiotic resistance is a major challenge in the clinical treatment of bacterial infectious diseases. Herein, we constructed a multifunctional DNA nanoplatform as a versatile carrier for bacteria‐specific delivery of clinical antibiotic ciprofloxacin (CIP) and classic nanoantibiotic silver nanoparticles (AgNP). In our rational design, CIP was efficiently loaded in the self‐assembly double‐bundle DNA tetrahedron through intercalation with DNA duplex, and single‐strand DNA‐modified AgNP was embedded in the cavity of the DNA tetrahedron through hybridization. With the site‐specific assembly of targeting aptamer in the well‐defined DNA tetrahedron, the bacteria‐specific dual‐antibiotic delivery system exhibited excellent combined bactericidal properties. With enhanced antibiotic accumulation through breaking the out membrane of bacteria, the antibiotic delivery system effectively inhibited biofilm formation and promoted the healing of infected wounds in vivo. This DNA‐based antibiotic delivery system provides a promising strategy for the treatment of antibiotic‐resistant infections.