METHODS AND DEVICES FOR THE PREPARATION OF NANOMATERIALS
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United States of America Patent
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app pub date -
Jun 19, 2017
filing date -
Jun 17, 2016
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Abstract
Disclosed herein are methods for preparing nanomaterials, such as nanoparticles. The methods can involve jet-mixing two or more precursor solutions to form the nanomaterials. By rapidly mixing the precursor solutions, nanomaterials of improved quality and uniformity can be prepared in high yield (e.g., in yields of at least 85%). The methods are also scalable, and allow for the continuous production of nanomaterials. Also provided are jet-mixing reactors that can be used to prepare nanomaterials using the methods described herein.
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- 15 United States
- 10 France
- 8 Japan
- 7 China
- 5 Korea
- 2 Other
Patent Owner(s)
Patent Owner | Address | |
---|---|---|
OHIO STATE INNOVATION FOUNDATION | 1524 NORTH HIGH STREET COLUMBUS OH 43201 |
International Classification(s)

- 2017 Application Filing Year
- C07F Class
- 1442 Applications Filed
- 965 Patents Issued To-Date
- 66.93 % Issued To-Date
Inventor(s)
Inventor Name | Address | # of filed Patents | Total Citations |
---|---|---|---|
Brunelli, Nicholas | Columbus, US | 3 | 7 |
# of filed Patents : 3 Total Citations : 7 | |||
Parulkar, Aamena | Columbus, US | 3 | 1 |
# of filed Patents : 3 Total Citations : 1 |
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- 0 Citation Count
- C07F Class
- 0 % this patent is cited more than
- 8 Age
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Full Text
- i. providing a composition comprising one or more ribonucleic acids molecules (RNA),ii. hybridizing to said one or more RNAs, one or more two-part nucleic acid hybridization probes, wherein each probe comprises, a. a first nucleic acid molecule with a 3′-tail wherein said tail does not hybridize to an RNA in the composition,b. a second nucleic acid molecule with a 5′-tail wherein said tail does not hybridize to an RNA in the composition,c. wherein said first and said second nucleic acid molecules when and if hybridized to their target RNA lie on one single stranded RNA molecule separated from each other by between 2 and 1000 nucleotides, iii. covalently linking the hybridized 5′-tail of said first nucleic acid molecule to the hybridized 3′-tail of said second nucleic acid, wherein the linking is done by means of reverse transcription and subsequent ligation,iv. amplifying the linked molecules with primers that are specific for said first 3′-tail of said first nucleic acid molecule and said second 5′-tail of said second nucleic acid molecule and,v. sequencing the amplification products by means of next generation sequencing.

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