Lactobacillus cell envelope-coated nanoparticles for antibiotic delivery against cariogenic biofilm and dental caries.

BACKGROUND: Due to their prevalence, dental caries ranks first among all diseases endangering human health. Therefore, the prevention of caries is of great significance, as caries have become a serious public health problem worldwide. Currently, using nanoscale drug delivery systems to prevent caries has received increased attention. However, the preventive efficacy of these systems is substantially limited due to the unique physiological structure of cariogenic biofilms. Thus, novel strategies aimed at combating cariogenic biofilms to improve preventive efficiency against caries are meaningful and very necessary. Herein, inspired by cell membrane coating technology and Lactobacillus strains, we coated triclosan (TCS)-loaded poly(lactic-co-glycolic acid) (PLGA) nanoparticles (TCS@PLGA-NPs) with an envelope of Lactobacillus (LA/TCS@PLGA-NPs) and investigated their potential as a nanoparticle delivery system against cariogenic biofilms and dental caries. RESULTS: LA/TCS@PLGA-NPs were successfully prepared with favorable properties, including a coated envelope, controllable size, negative charge, sustained drug-release kinetics and so on. The LA/TCS@PLGA-NPs inherited native properties from the source cell surface, thus the LA/TCS@PLGA-NPs adhered to S. mutans, integrated into the S. mutans biofilm, and interfered with the biofilm formation of S. mutans. The nanoparticles significantly inhibited the activity, biomass and virulence gene expression of S. mutans biofilms in vitro. Additionally, LA/TCS@PLGA-NPs exhibited a long-lasting inhibitory effect on the progression of caries in vivo. The safety performance of the nanoparticles is also favorable. CONCLUSIONS: Our findings reveal that the antibiofilm effect of LA/TCS@PLGA-NPs relies not only on the inheritance of native properties from the Lactobacillus cell surface but also on the inhibitory effect on the activity, biomass and virulence of S. mutans biofilms. Thus, these nanoparticles could be considered feasible candidates for a new class of effective drug delivery systems for the prevention of caries. Furthermore, this work provides new insights into cell membrane coating technology and presents a novel strategy to combat bacterial biofilms and associated infections.

Selective and rapid removal of Mo(VI) from water using functionalized Fe3O4-based Mo(VI) ion-imprinted polymer.

Fe3O4 nanoparticles-based magnetic Mo(VI) surface ion-imprinted polymer (Mo(VI)-MIIP) was elaborated employing 4-vinyl pyridine as a functional monomer. The adsorbent preparation was confirmed by Fourier-transform infrared spectroscopy, scanning electron microscopy, energy dispersive X-ray spectrometry, X-ray diffraction, vibrating sample magnetometer, thermogravimetric analysis, and surface area analysis. Batch adsorption experiments showed that the maximum adsorption capacity of Mo(VI)-MIIP was 296.40 mg g-1 at pH 3, while that of the magnetic non-imprinted polymer (MNIP) was only 147.10 mg g-1. The adsorption isotherm model was well fitted by the Langmuir isotherm model. The adsorption experiments revealed that Mo(VI)-MIIP reached adsorption equilibrium within 30 min, and the kinetics data fitting showed that the pseudo-second-order kinetics model suitably described the adsorption process. Mo(VI)-MIIP exhibited an excellent adsorption selectivity to Mo(VI) in binary mixtures of Mo(VI)/Cr(VI), Mo(VI)/Cu(II), Mo(VI)/H2PO44-, Mo(VI)/Zn(II), and Mo(VI)/I-, with relative selectivity coefficients toward MNIP of 13.71, 30.27, 20.01, 23.53, and 15.89, respectively. After six consecutive adsorption-desorption cycles, the adsorption capacity of Mo(VI)-MIIP decreased by 9.5% (from 228.4 mg g-1 to 206.7 mg g-1 at initial Mo(VI) concentration of 250 mg L-1), demonstrating its reusability.