4.7 Article

Controlled Synthesis of Up-Conversion NaYF4:Yb,Tm Nanoparticles for Drug Release under Near IR-Light Therapy

期刊

BIOMEDICINES
卷 9, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/biomedicines9121953

关键词

Up-Conversion; drug-delivery; Near IR-Light Therapy

资金

  1. European Union's Horizon 2020 research and innovation program under European Research Council (ERC) through the HyMAP project [648319]
  2. AEI-MICINN/FEDER, UE through the Nympha Project [PID2019-106315RB-I00]
  3. Generalitat Valenciana [CIDEGENT/2018/044]

向作者/读者索取更多资源

The study focused on the application of NaYF4:Yb,Tm up-converted material in drug release, achieving excellent luminescence properties through controlled synthesis conditions, and promoting research and development in light-driven drug release systems.
Up-Conversion materials have received great attention in drug delivery applications in recent years. A specifically emerging field includes the development of strategies focusing on photon processes that promote the development of novel platforms for the efficient transport and the controlled release of drug molecules in the harsh microenvironment. Here, modified reaction time, thermal treatment, and pH conditions were controlled in the synthesis of NaYF4:Yb,Tm up-converted (UC) material to improve its photoluminescence properties. The best blue-emission performance was achieved for the UC3 sample prepared through 24 h-synthesis without thermal treatment at a pH of 5, which promotes the presence of the beta-phase and smaller particle size. NaYF4:Yb,Tm has resulted in a highly efficient blue emitter material for light-driven drug release under near-IR wavelength. Thus, NaYF4:Yb,Tm up-converted material promotes the N-O bond cleavage of the oxime ester of Ciprofloxacin (prodrug) as a highly efficient photosensitized drug delivery process. HPLC chromatography and transient absorption spectroscopy measurements were performed to evaluate the drug release conversion rate. UC3 has resulted in a very stable and easily recovered material that can be used in several reaction cycles. This straightforward methodology can be extended to other drugs containing photoactive chromophores and is present as an alternative for drug release systems.

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