Abstract

BackgroundX-ray computed tomography (CT) imaging can be used to reveal the three-dimensional structure of deep tissue with high spatial resolution. However, it cannot reveal molecular or cellular changes, and has great limitations in terms of specificity and sensitivity. Fluorescence imaging technology is one of the main methods used for the study of molecular events in vivo and has important applications in life science research. Therefore, the combination of CT and fluorescence imaging is an ideal dual-modal molecular imaging method, which can provide data on both molecular function and tissue structure, and has important research value. In a previous study, Bi2S3 nanoparticles were wrapped with quantum dots in SiO2 to generate CT and fluorescence imaging. However, this type of probe led to low survival and caused innegligible in vivo toxicity in mice. Therefore, it is necessary to develop new multifunctional probes that demonstrate biocompatibility and safety in vivo.MethodsA polyethylene glycol-phospholipid bilayer structure was used to synthesize hybrid clusters containing hydrophobic Bi2S3 nanoparticles and quantum dots for combined CT/fluorescence imaging. Mean particle size, polydispersity index, and zeta potential were used to study the stability over an 8-week test period. In vivo CT and fluorescence imaging experiments were performed, and the in vivo safety of the probe was evaluated, using histopathological, biochemical, and blood analyses.ResultsThe probe distinctly enhanced the CT contrast and had fluorescence imaging capability. In addition, the nanocomposite hybrid clusters showed a longer circulation time (>4 h) than iobitridol. The results also showed that the Bi2S3-QD@DSPE probe had good biocompatibility and safety, and did not affect normal organ functioning.ConclusionsBi2S3-QD@DSPE hybrid clusters exhibited remarkable performance in CT angiography and fluorescence imaging in vivo.

Highlights

  • X-ray computed tomography (CT) imaging can be used to reveal the three-dimensional structure of deep tissue with high spatial resolution

  • Fluorescence imaging technology is one of the main methods used in the study of molecular events in vivo and has important applications in life science research

  • The results showed that the Bi2S3-quantum dots (QDs)@DSPE probes show good biocompatibility and safety, and did not affect normal organ functioning

Read more

Summary

Methods

Materials Bismuth neodecanote, oleic acid (90 %), cadmium oxide (99.99 %), bis(trimethylsilyl) sulfide ((TMS)2S), hexadecylamine (90 %), tri-n-octylphosphine oxide (90 %), and trioctylphosphine (97 %) were purchased from Aldrich. Oleyl amine (90 %) was purchased from Aladdin. Thioacetamide and selenium powder were purchased from Sinopharm. 1,2-Dipalmitoyl-sn-glycero3-phosphoethanol-amine-N-[methoxy(polyethylene glycol)-2000] (PEG-DSPE, 99 %) was purchased from Avanti. All chemicals were used as received, unless otherwise stated. Characterization Nanoparticle spectra were measured using a 2550 UV– visible spectrophotometer (Japan) and a LS-55 spectrophotometer (USA). Elemental analysis of the resultant hybrid clusters was performed using an inductively coupled plasma atomic emission spectrometer (Germany). Animal blood analysis was carried out on a SP-4430 dry biochemical analyzer (Japan) and a CA-700 automatic blood analyzer (China). TEM images were captured using a Tecnai G20 U-Twin transmission electron microscope (USA). Had no significant effect on organs, tissues, or blood, and showed remarkable biocompatibility and promise as a contrast agent

Results
Background
Results and discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call