In Situ Embedding Synthesis of Highly Stable CsPbBr 3 /CsPb 2 Br 5 @PbBr(OH) Nano/Microspheres through Water Assisted Strategy

2021 ◽  
pp. 2103275
Author(s):  
Kaimin Du ◽  
Lingjun He ◽  
Shuyan Song ◽  
Jing Feng ◽  
Yao Li ◽  
...  
Keyword(s):  
1991 ◽  
Vol 66 (5) ◽  
pp. 269-272 ◽  
Author(s):  
A. Beatrice Murray ◽  
Helga Schulze ◽  
Elisabeth Blauw

1971 ◽  
Vol 50 (3) ◽  
pp. 691-708 ◽  
Author(s):  
N. Scott McNutt ◽  
Lloyd A. Culp ◽  
Paul H. Black

The ultrastructural appearances of normal 3T3, SV40-transformed 3T3 (SV-3T3), and F1A revertant cell lines are compared. Both confluent and subconfluent cultures are described after in situ embedding of the cells for electron microscopy. There is striking nuclear pleomorphism in F1A revertant cells, with many cells having large nuclei compared to the less variable nuclear morphology of both normal 3T3 and SV-3T3 cells. Under the culture conditions used, deep infoldings of the nuclear envelope are prominent in growing cells, e.g., subconfluent normal 3T3 and confluent SV-3T3 cells. Such infoldings are infrequently seen in cultures which display contact inhibition of growth, e.g., normal 3T3 or F1A revertant cells grown just to confluence. In confluent cultures, the cytoplasmic organelles in revertant cells closely resemble those of normal 3T3 cells. In both normal and revertant cells in confluent culture, the peripheral cytoplasm (ectoplasm) has many 70 A filaments (alpha filaments), which are frequently aggregated into bundles. Alpha filaments are also abundant in the ectoplasm near regions of cell-to-cell apposition and in the motile cell processes (filopodia). The abundance and state of aggregation of alpha filaments correlates with contact inhibition of movement and growth in these cell lines since fewer bundles of alpha filaments are seen in growing cells than in contact-inhibited cells. This observation suggests that these filaments may be an important secondary component in the regulation of contact inhibition of movement and, possibly, of growth in normal and revertant cells.


1988 ◽  
Vol 150 (2) ◽  
pp. 161-163 ◽  
Author(s):  
G. BOU-Gharios ◽  
G. Adams ◽  
J. Moss ◽  
I. Shore ◽  
I. Olscen

2014 ◽  
Vol 118 (41) ◽  
pp. 23635-23644 ◽  
Author(s):  
Yongtao Li ◽  
Luxing Zhang ◽  
Qingan Zhang ◽  
Fang Fang ◽  
Dalin Sun ◽  
...  

Author(s):  
Manoj Malviya ◽  
Swapnil Sinha ◽  
Nicholas A. Meisel

Abstract Additive manufacturing (AM) offers access to the entire volume of a printed artifact during the build operation. This makes it possible to embedding foreign components (e.g. sensors, motors, actuators) into AM parts, thus enabling multifunctional products directly from the build tray. However, the process of designing for embedding currently requires extensive designer expertise in AM. Current methods rely on a designer to select an orientation for the embedded component and design a cavity such that the component can be successfully embedded without compromising the print quality of the final part. For irregular geometries, additional design knowledge is required to prepare a shape converter: a secondary piece to ensure a flush deposition surface on top of the embedded component. This research aims to develop a tool to automate these different design decisions for in-situ embedding, thus reducing the need for expert design knowledge. A three-stage process is proposed to 1) find the optimum orientation based on cavity volume and cross-section area, 2) create the necessary cavity geometry to successfully insert the component, and 3) perform a Boolean operation to create the digital design for any requisite shape converter. Performance of the tool is demonstrated with four test cases with varying levels of geometric complexity. These test cases show that the proposed process successfully handles arbitrary embedded geometries, though several limitations are noted for future work.


Author(s):  
Kai Chien

Untreated glass is the ideal supporting substrate for cell cul¬ture growth since it is extremely flat and smooth, transparent and insoluable in organic solvent. However, difficulties have been encountered in removing polymerized epoxy resin from a glass surface following in situ cell monolayer embedment. Vari¬ous techniques have been made to grow cell cultures on either coated glass surfaces or plastic substrates. The purpose of this abstract is to describe a heat separation technique which when used together with a newly designed embedding mold allows cell monolayers to be transferred from untreated coverglass or glass slide to pre-shaped tissue blocks. The resulting tissue block can be easily separated and used directly for orientation light microscopy prior to ultramicrotomy.


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