Self-assembling of multi-jets by pyro-electrohydrodynamic effect for high throughput liquid nanodrops transfer

Lab on a Chip ◽  
2011 ◽  
Vol 11 (19) ◽  
pp. 3294 ◽  
Author(s):  
Sara Coppola ◽  
Veronica Vespini ◽  
Simonetta Grilli ◽  
Pietro Ferraro
RSC Advances ◽  
2018 ◽  
Vol 8 (38) ◽  
pp. 21272-21279 ◽  
Author(s):  
Guangxia Feng ◽  
Qinghua He ◽  
WenYue Xie ◽  
Yonghong He ◽  
Xuejing Chen ◽  
...  

The rapid growth of demand for high-throughput multiplexed biochips from modern biotechnology has led to growing interest in suspension array based on multi-channel encoded microbeads.


RSC Advances ◽  
2020 ◽  
Vol 10 (69) ◽  
pp. 42529-42541
Author(s):  
Kristof Toth ◽  
Chinedum O. Osuji ◽  
Kevin G. Yager ◽  
Gregory S. Doerk

Compositionally graded electrospray deposition combined with grazing incidence small angle X-ray scattering forms a high-throughput approach for mapping phase behavior in ternary mixtures as demonstrated here using block copolymer blends.


Author(s):  
Daniel Reker ◽  
Yulia Rybakova ◽  
Ameya R. Kirtane ◽  
Ruonan Cao ◽  
Jee Won Yang ◽  
...  

2019 ◽  
Author(s):  
Daniel Reker ◽  
Yulia Rybakova ◽  
Ameya R. Kirtane ◽  
Ruonan Cao ◽  
Jee Won Yang ◽  
...  

AbstractNanoformulations are transforming our capacity to effectively deliver and treat a myriad of conditions. However, many nanoformulation approaches still suffer from high production complexity and low drug loading. One potential solution relies on harnessing co-assembly of drugs and small molecular excipients to facilitate nanoparticle formation through solvent exchange without the need for chemical synthesis, generating nanoparticles with up to 95% drug loading. However, there is currently no understanding which of the millions of possible combinations of small molecules can result in the formation of these nanoparticles. Here we report the development of a high-throughput screening platform coupled to machine learning to enable the rapid evaluation of such nanoformulations. Our platform identified 101 novel self-assembling drug nanoparticles from 2.1 million pairings derived from 788 candidate drugs with one of 2686 excipients, spanning treatments for multiple diseases and often harnessing well-known food additives, vitamins, or approved drugs as carrier materials – with potential for accelerated approval and translation. Given their long-term stability and potential for clinical impact, we further characterize novel sorafenib-glycyrrhizin and terbinafine-taurocholic acid nanoparticles ex vivo and in vivo. We anticipate that this platform could accelerate the development of safer and more efficacious nanoformulations with high drug loadings for a wide range of therapeutics.


RSC Advances ◽  
2014 ◽  
Vol 4 (92) ◽  
pp. 50393-50400 ◽  
Author(s):  
Wenhui Chen ◽  
Jun Luo ◽  
Peixiong Shi ◽  
Chunlong Li ◽  
Xiaobin He ◽  
...  

Directed self-assembly (DSA), an emerging lithographic technique, has attracted increasing attention as a result of its advantages of low cost, high throughput and convenient processing.


2021 ◽  
Author(s):  
Changyang Linghu ◽  
Bobae An ◽  
Monika Shpokayte ◽  
Orhan T. Celiker ◽  
Nava Shmoel ◽  
...  

Observing cellular physiological histories is key to understanding normal and disease-related processes, but longitudinal imaging is laborious and equipment-intensive. A tantalizing possibility is that cells could record such histories in the form of digital biological information within themselves, for later high-throughput readout. Here we show that this concept can be realized through information storage in the form of growing protein chains made out of multiple self-assembling subunits bearing different labels, each corresponding to a different cellular state or function, so that the physiological history of the cell can be visually read out along the chain of proteins. Conveniently, such protein chains are fully genetically encoded, and easily readable with simple, conventional optical microscopy techniques, compatible with visualization of cellular shape and molecular content. We use such expression recording islands (XRIs) to record gene expression timecourse downstream of pharmacological and physiological stimuli, in cultured neurons and in living mouse brain.


Author(s):  
George C. Ruben ◽  
Kenneth A. Marx

Certain double stranded DNA bacteriophage and viruses are thought to have their DNA organized into large torus shaped structures. Morphologically, these poorly understood biological DNA tertiary structures resemble spermidine-condensed DNA complexes formed in vitro in the total absence of other macromolecules normally synthesized by the pathogens for the purpose of their own DNA packaging. Therefore, we have studied the tertiary structure of these self-assembling torus shaped spermidine- DNA complexes in a series of reports. Using freeze-etch, low Pt-C metal (10-15Å) replicas, we have visualized the microscopic DNA organization of both calf Thymus( CT) and linear 0X-174 RFII DNA toruses. In these structures DNA is circumferentially wound, continuously, around the torus into a semi-crystalline, hexagonal packed array of parallel DNA helix sections.


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