hollow shell
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2022 ◽  
Vol 571 ◽  
pp. 151337
Author(s):  
Lin Lyu ◽  
Quan Xie ◽  
Yinye Yang ◽  
Rongrong Wang ◽  
Weifu Cen ◽  
...  

Nanomaterials ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2455
Author(s):  
Manuel Pérez-Garnes ◽  
Victoria Morales ◽  
Raul Sanz ◽  
Rafael A. García-Muñoz

Among the different types of nanoparticles used in biomedical applications, Fe nanoparticles and mesoporous siliceous materials have been extensively investigated because of their possible theranostic applications. Here, we present hollow-shell mesoporous silica nanoparticles that encapsulate iron oxide and that are prepared using a drug-structure-directing agent concept (DSDA), composed of the model drug tryptophan modified by carbon aliphatic hydrocarbon chains. The modified tryptophan can behave as an organic template that allows directing the hollow-shell mesoporous silica framework, as a result of its micellisation and subsequent assembly of the silica around it. The one-pot synthesis procedure facilitates the incorporation of hydrophobically stabilised iron oxide nanoparticles into the hollow internal silica cavities, with the model drug tryptophan in the shell pores, thus enabling the incorporation of different functionalities into the all-in-one nanoparticles named mesoporous silica nanoparticles containing magnetic iron oxide (Fe3O4@MSNs). Additionally, the drug loading capability and the release of tryptophan from the silica nanoparticles were examined, as well as the cytostaticity and cytotoxicity of the Fe3O4@MSNs in different colon cancer cell lines. The results indicate that Fe3O4@MSNs have great potential for drug loading and drug delivery into specific target cells, thereby overcoming the limitations associated with conventional drug formulations, which are unable to selectively reach the sites of interest.


2021 ◽  
pp. 103796
Author(s):  
Oscar Figueras-Alvarez ◽  
Lucas Queiroz Caponi ◽  
Francisco Real-Voltas

2021 ◽  
Author(s):  
Sohyung Lee ◽  
Joe de Rutte ◽  
Robert Dimatteo ◽  
Doyeon Koo ◽  
Dino Di Carlo

Microparticles with defined shapes and spatial chemical modification can enable new opportunities to interface with cells and tissues at the cellular scale. However, conventional methods to fabricate shaped microparticles have trade-offs between the throughput of manufacture and precision of particle shape and chemical functionalization. Here, we achieved scalable production of hydrogel microparticles at rates of greater than 40 million/hour with localized surface chemistry using a parallelized step emulsification device and temperature-induced phase-separation. The approach harnesses a polymerizable polyethylene glycol (PEG) and gelatin aqueous-two phase system (ATPS) which conditionally phase separates within microfluidically-generated droplets. Following droplet formation, phase separation is induced and phase separated droplets are subsequently crosslinked to form uniform crescent and hollow shell particles with gelatin functionalization on the boundary of the cavity. The gelatin localization enabled deterministic cell loading in nanoliter-sized crescent-shaped particles, which we refer to as nanovials, with cavity dimensions tuned to the size of cells. Loading on nanovials also imparted improved cell viability during analysis and sorting using standard fluorescence activated cell sorters, presumably by protecting cells from shear stress. This localization effect was further exploited to selectively functionalize capture antibodies to nanovial cavities enabling single-cell secretion assays with reduced cross-talk in a simplified format.


Catalysts ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 582
Author(s):  
Abdulelah Taher Ali Mohammed ◽  
Lijian Wang ◽  
Ronghua Jin ◽  
Guohua Liu ◽  
Chunxia Tan

The construction of a high stability heterogeneous catalyst for privileged common catalysis is a benefit in regard to reuse and separation. Herein, a palladium diphenylphosphine-based hollow-shell-structured mesoporous catalyst (HS@PdPPh2@MSN) was prepared by immobilizing bis((diphenylphosphino)ethyltriethoxysilane)palladium acetate onto the inner wall of a mesoporous organicsilicane hollow shell, whose surface was protected by a –Si(Me)3 group. Electron microscopies confirmed its hollow-shell-structure, and structural analyses and characterizations revealed its well-defined single-site active species within the silicate network. As presented in this study, the newly constructed HS@PdPPh2@MSN enabled an efficient Suzuki-Miyaura cross-coupling reaction for varieties of substrates with up to 95% yield in mild conditions. Meanwhile, it could be reused at least five times with good activity, indicating its excellent stability and recyclability. Furthermore, the cost-effective and easily synthesized HS@PdPPh2@MSN made it a good candidate for employment in fine chemical engineering.


2021 ◽  
Vol 30 (2) ◽  
pp. 025042
Author(s):  
Luonan Zhou ◽  
Xiaoyang Zheng ◽  
Kai Du ◽  
Xiaofeng Guo ◽  
Qiang Yin ◽  
...  
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2020 ◽  
Vol 8 ◽  
Author(s):  
Xiaohuan Sun ◽  
Jie Han ◽  
Rong Guo

Yolk-shell structured nanomaterials, possessing a hollow shell and interior core, are emerging as unique nanomaterials with applications ranging from material science, biology, and chemistry. In particular, the scaffold yolk-shell structure shows great promise as a nanocatalyst. Specifically, the hollow shell offers a confined space, which keeps the active yolk from aggregation and deactivation. The inner void ensures the pathway for mass transfer. Over the last few decades, many strategies have been developed to endow yolk-shell based nanomaterials with superior catalytic performance. This minireview describes synthetic methods for the preparation of various yolk-shell nanomaterials. It discusses strategies to improve the performance of yolk-shell catalysts with examples for engineering the shell, yolk, void, and related synergistic effects. Finally, it considers the challenges and prospects for yolk-shell nanocatalysts.


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