Lanthanide-Doped Core–Shell–Shell Nanocomposite for Dual Photodynamic Therapy and Luminescence Imaging by a Single X-ray Excitation Source

2018 ◽  
Vol 10 (9) ◽  
pp. 7859-7870 ◽  
Author(s):  
Chang-Chieh Hsu ◽  
Syue-Liang Lin ◽  
C. Allen Chang
2010 ◽  
Vol 1257 ◽  
Author(s):  
Juan C. Beltran Huarac ◽  
Surinder P. Singh ◽  
Maharaj S. Tomar ◽  
Sandra Peňa ◽  
Luis Rivera ◽  
...  

AbstractThe use of nanoparticles as carriers of photosensitizer (PS) molecules for photodynamic therapy (PDT) has attracted much interest on core-shell nanosize structures. Herein, we used a simple aqueous solution method to synthesize Fe3O4/ZnO core-shell nanoparticles. X-ray diffraction (XRD) analyses showed the presence of well defined peaks corresponding to Fe3O4 and ZnO in as-synthesized nanocrystals. Vibrating sample magnetometer (VSM) measurements showed that these nanoparticles exhibited superparamagnetic behavior of the core with no coercivity nor remanence. X-ray photoelectron spectroscopy (XPS) analyses revealed the presence of Zn1/2 and Zn3/2 species on the surface of nanocrystals. Photoluminescence measurements showed excitonic emission of ZnO co-existing with a weak and broad defect- related green emission at room temperature. The generation of singlet oxygen was monitored via the photooxidation of diphenyl-1,3-isobenzofuran (DPBF) with different light sources, followed by absorption spectroscopy at 409 nm. The capability of synthesized nanoparticles to generate singlet oxygen has also been verified.


2021 ◽  
Vol 53 (5) ◽  
pp. 494-508
Author(s):  
Anja Müller ◽  
Thoralf Krahl ◽  
Jörg Radnik ◽  
Andreas Wagner ◽  
Carsten Kreyenschulte ◽  
...  

2020 ◽  
Vol 18 (1) ◽  
Author(s):  
Xuefan Gu ◽  
Chao Shen ◽  
Hua Li ◽  
Ewa M. Goldys ◽  
Wei Deng

Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 730
Author(s):  
Erik Sarnello ◽  
Tao Li

Enzyme immobilization techniques are widely researched due to their wide range of applications. Polymer–protein core–shell nanoparticles (CSNPs) have emerged as a promising technique for enzyme/protein immobilization via a self-assembly process. Based on the desired application, different sizes and distribution of the polymer–protein CSNPs may be required. This work systematically studies the assembly process of poly(4-vinyl pyridine) and bovine serum albumin CSNPs. Average particle size was controlled by varying the concentrations of each reagent. Particle size and size distributions were monitored by dynamic light scattering, ultra-small-angle X-ray scattering, small-angle X-ray scattering and transmission electron microscopy. Results showed a wide range of CSNPs could be assembled ranging from an average radius as small as 52.3 nm, to particles above 1 µm by adjusting reagent concentrations. In situ X-ray scattering techniques monitored particle assembly as a function of time showing the initial particle growth followed by a decrease in particle size as they reach equilibrium. The results outline a general strategy that can be applied to other CSNP systems to better control particle size and distribution for various applications.


Theranostics ◽  
2016 ◽  
Vol 6 (13) ◽  
pp. 2295-2305 ◽  
Author(s):  
Geoffrey D. Wang ◽  
Ha T. Nguyen ◽  
Hongmin Chen ◽  
Phillip B. Cox ◽  
Lianchun Wang ◽  
...  
Keyword(s):  

2017 ◽  
Vol 55 (15) ◽  
pp. 2513-2526 ◽  
Author(s):  
Florent Jasinski ◽  
Victoria L. Teo ◽  
Rhiannon P. Kuchel ◽  
Monique Mballa Mballa ◽  
Stuart C. Thickett ◽  
...  

2021 ◽  
Vol 1040 ◽  
pp. 61-67
Author(s):  
Anna B. Vlasenko ◽  
Vadim V. Bakhmetyev ◽  
Sergey V. Mjakin

Photodynamic therapy (PDT) is a promising modern method for treatment of oncological, bacterial, fungal and viral diseases. However, its application is limited to diseases with superficial localization since the body tissues are not transparent for visible light. To address this problem and extend PDT application to abdominal diseases, an enhanced method of X-ray photodynamic therapy (XRPDT) is suggested, involving X-ray radiation easily penetrating the body tissues. The implementation of this approach requires the development of a pharmacological drug including a photosensitizer stimulated by visible light to yield active oxygen and a nanosized phosphor converting X-ray radiation into visible light with the wavelength required for the photosensitizer activation. This study is aimed at obtaining X-ray stimulated phosphors with nanosized particles suitable for XRPDT application. For this purpose, Y2O3:Eu phosphors were synthesized via hydrothermal processing of the corresponding mixed acetate followed by annealing. To prevent from the undesirable agglomeration of the particles in the course of hydrothermal synthesis and subsequent annealing, different techniques were used, including rapid thermal annealing (RTA), microwave annealing and addition of finely dispersed pyrogenic silica (aerosil) to the phosphor. The microwave annealing was carried out using a special installation including a resonance chamber for maintaining a standing wave of microwave radiation. The performed research allowed the determination of hydrothermal processing optimal duration affording the synthesis of phosphors with the highest luminescence brightness. The application of microwave annealing is found to provide phosphors with a more perfect crystal structure compared with RTA. The developed method of Y2O3:Eu phosphor synthesis involving pyrogenic silica addition to the autoclave allowed the preparation of samples with the amorphous structure and significantly reduced the particle size without a considerable decrease in the luminescence brightness. The particle size of the phosphor synthesized with aerosil addition is less than 100 nm that allows its implementation in pharmacological drugs for XRPDT.


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