Magneto-Based Synergetic Therapy for Implant-Associated Infections via Biofilm Disruption and Innate Immunity Regulation.
Jiaxing WangLingtian WangJiong PanJinhui ZhaoJin TangDajun JiangPing HuWeitao JiaJianlin ShiPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2021)
Implant-associated infections (IAIs) are a common cause of orthopedic surgery failure due to microbial biofilm-induced antibiotic-resistance and innate immune inactivation. Thus, the destruction of microbial biofilm plays a key role in reducing IAIs. Herein, first, a magneto-based synergetic therapy (MST) is proposed and demonstrated against IAIs based on biofilm destruction. Under an alternating magnetic field (AMF), CoFe2O4@MnFe2O4 nanoparticles (MNPs), with a rather strong magnetic hyperthermal capacity, can generate sufficient thermal effect to cause dense biofilm dispersal. Loosened biofilms provide channels through which nitrosothiol-coated MNPs (MNP-SNOs) can penetrate. Subsequently, thermosensitive nitrosothiols rapidly release nitric oxide (NO) inside biofilms, thus efficiently killing sessile bacteria under the magnetothermal effect of MNPs. More importantly, MNP-SNOs can trigger macrophage-related immunity to prevent the relapse of IAIs by exposing the infected foci to a consistent innate immunomodulatory effect. The notable anti-infection effect of this nanoplatform is also confirmed in a rat IAI model. This work presents the promising potential of combining magnetothermal therapy with immunotherapy, for the effective and durable control and elimination of IAIs.
Keyphrases
- candida albicans
- pseudomonas aeruginosa
- staphylococcus aureus
- biofilm formation
- nitric oxide
- innate immune
- cystic fibrosis
- microbial community
- minimally invasive
- stem cells
- adipose tissue
- escherichia coli
- oxidative stress
- acute coronary syndrome
- mesenchymal stem cells
- diabetic rats
- risk assessment
- soft tissue
- bone marrow
- drug induced
- drug release
- free survival
- smoking cessation
- liquid chromatography
- simultaneous determination
- molecularly imprinted