| Nanomaterials possess many excellent properties because of the unique physical and chemical properties,which have been applied in various fields such as biomedicine.In this paper,the photothermal and photodynamic properties of Ti3C2nanosheets,gold nanorods(GNRs)and polydopamine(PDA)were used to prepare two kinds of nanomaterials with different properties.An in-situ growth approach was employed to combine GNRs with Ti3C2 nanosheets to prepare in-situ Ti3C2@GNRs.Based on in-situ Ti3C2@GNRs,Ti3C2@GNRs/PDA/Ti3C2 nanocarriers with excellent photothermal properties,photothermal stability,drug loading rate,p H/NIR dual responsive drug release performance and biocompatibility were prepared.Also,Ti3C2@GNRs/PDA hybrid nanoparticles with distinct synergistic photodynamic antibacterial properties were prepared in this paper.This thesis is divided into the following two parts.Firstly,Ti3C2@GNRs were obtained by in-situ growth of GNRs on the surface of Ti3C2 nanosheets.Due to the excellent photothermal synergy between GNRs and Ti3C2 nanosheets,Ti3C2@GNRs displayed high photothermal conversion efficiency(45.89%).Next,in order to improve the drug loading rate of nanocarriers,Ti3C2nanosheets and Ti3C2@GNRs were combined by using the distinct adhesion of PDA to form sandwich-like Ti3C2@GNRs/PDA/Ti3C2 nanocarriers.In addition,the dispersibility and stability of Ti3C2@GNRs/PDA/Ti3C2nanocarriers in different media were significantly improved by modifying with SH-PEG-CH3.The results of UV-Vis-NIR,XRD,FT-IR,XPS,SEM,TEM and AFM indicated the successful preparation of Ti3C2@GNRs/PDA/Ti3C2 nanocarriers.And the size of Ti3C2@GNRs/PDA/Ti3C2 nanocarriers was around 200-300 nm.GNRs were inserted between Ti3C2 nanosheets,which could better reflect the near-infrared(NIR)responsiveness of two-dimensional Ti3C2 nanosheets.In addition,there were significant synergistic photothermal effects between Ti3C2 and GNRs.Therefore,Ti3C2@GNRs/PDA/Ti3C2 nanosheets exhibited excellent NIR response properties.The high specific surface area of Ti3C2 nanosheets and the strong adhesion of PDA endowed Ti3C2@GNRs/PDA/Ti3C2 nanocarriers with high drug loading efficiency(95.88%).Furthermore,due to the strongπ-πinteraction between Ti3C2@GNRs/PDA/Ti3C2 and DOX,Ti3C2@GNRs/PDA/Ti3C2 nanocarriers displayed p H/NIR dual responsive drug release properties under the NIR laser irradiation.Moreover,the results of cytotoxicity tests indicated that Ti3C2@GNRs/PDA/Ti3C2 nanocarriers possessed low cytotoxicity and excellent biocompatibility.Then,the application of Ti3C2@GNRs/PDA hybrid nanoparticles in the field of synergistic photodynamic antibacterial was evaluated.In order to obtain nanoparticles with better synergistic photodynamic antibacterial properties,Ti3C2@GNRs hybrid nanoparticles with smaller size was prepared by extending the ultrasonic time of Ti3C2@GNRs.Then,Ti3C2@GNRs were modified with SH-PEG-CH3 to obtain highly stable Ti3C2@GNRs-PEG.Finally,DA self-polymerized on the surface of Ti3C2@GNRs to form Ti3C2@GNRs/PDA hybrid nanoparticles under alkaline conditions.In addition,Ti3C2@GNRs/PDA hybrid nanoparticles with different PDA contents were prepared by changing the concentration of DA.The successful preparation of Ti3C2@GNRs/PDA hybrid nanoparticles was verified by the results of FESEM,TEM,UV-Vis-NIR,Zeta potential,XPS and FT-IR.And the size of Ti3C2@GNRs/PDA hybrid nanoparticles was around 100 nm.Subsequently,the photodynamic properties and synergistic photodynamic antibacterial properties of Ti3C2@GNRs/PDA hybrid nanoparticles were investigated.The results indicated that inserted GNRs between Ti3C2 could effectively prevent the aggregation of two-dimensional Ti3C2 nanosheets,ensuring the excellent photodynamic properties of Ti3C2 and PDA.Therefore,Ti3C2@GNRs/PDA hybrid nanoparticles exhibited enhanced synergistic photodynamic properties.With the increase of PDA content,Ti3C2@GNRs/PDA could produce more amounts of 1O2.In the absence of antibiotics,Ti3C2@GNRs/PDA hybrid nanoparticles showed excellent synergistic antibacterial properties against both E.coli and S.aureus,exhibiting great potential in antibiotic-free antibacterial activities. |