4.8 Article

Compact, Programmable, and Stable Biofunctionalized Upconversion Nanoparticles Prepared through Peptide-Mediated Phase Transfer for High-Sensitive Protease Sensing and in Vivo Apoptosis Imaging

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 7, 期 22, 页码 11849-11856

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b01446

关键词

upconversion nanoparticle; phase transfer; peptide; protease; in vivo imaging; biosensing

资金

  1. National Natural Science Foundation of China (NSFC) [21175147, 91313302, 21475093]
  2. National High-Tech Research and Development Program [2014AA020518]
  3. 1000-Young Talents Plan
  4. PSTI of Suzhou [SZS201207]
  5. PAPD
  6. startup funds from Soochow University

向作者/读者索取更多资源

Protease represents an important class of biomarkers for disease diagnostics and drug screening. Conventional fluorescence-based probes for in vivo protease imaging suffer from short excitation wavelengths and poor photostability. Upconversion nanoparticles (UCNPs) hold great promise for biosensing and bioimaging because of their deep-tissue excitability, robust photostability, and minimal imaging background. However, producing highly stable and compact biofunctionalized UCNP probes with optimal bioresponsivity for in vivo imaging of protease activities still remains challenging and has not been previously demonstrated. Herein, we report facile preparation of highly compact and stable biofunctionalized UCNPs through peptide-mediated phase transfer for high-sensitive detection of protease in vitro and in vivo. We demonstrate that the polyhistidine-containing chimeric peptides could displace oleic acid molecules capped on UCNPs synthesized in organic solvents and, thereby, directly transfer UCNPs from the chloroform phase to the water phase. The resulting UCNPs possess high stability, programmable surface properties, and a compact coating layer with minimized thickness for efficient luminescence resonance energy transfer (LRET). On the basis of this strategy, we prepared LRET-based UCNP probes with optimal bioresponsivity for in vitro high-sensitive detection of trypsin and in vivo imaging of apoptosis for chemotherapy efficacy evaluation. The reported strategy could be extended to construct a variety of peptide-functionalized UCNPs for various biomedical applications.

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