Dota synthesis
US-2018370925-A1 · Dec 27, 2018 · US
US11027217B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11027217-B2 |
| Application number | US-201716313666-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 27, 2017 |
| Priority date | Jun 27, 2016 |
| Publication date | Jun 8, 2021 |
| Grant date | Jun 8, 2021 |
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Disclosed herein are systems and methods for the controlled crystallization of a compound. The controlled crystallization is achieved by applying an electric field across solutions of target compound and precipitant, whereby the electric field controls the rate of mixing.
Opening claim text (preview).
What is claimed is: 1. A crystallization system, comprising: at least one receiving member comprising a first electrically conductive member; at least one dispensing member comprising a second electrically conductive member, wherein the second electrical member is affixed to the receiving member; wherein the first and second electrical members are coupled in electrical communication; wherein the dispensing member comprises: an electrically insulating material proximal to the receiving member, a portion of the electrically insulating material defining at least one aperture, said portion in fluid communication with a receiving chamber; and whereby a complete electric circuit is obtained when electrolytes are present in the receiving and dispensing members. 2. The system according to claim 1 , wherein the portion defining at least one aperture has a dimension or surface area from 1 nm 2 to 20 μm 2 . 3. The system according to claim 1 , comprising a single dispensing member. 4. The system according to claim 1 , comprising a plurality of dispensing members. 5. The system according to claim 1 , wherein the dispensing body comprises an elongated body terminating at one end with the portion of the electrically insulating material defining at least one aperture. 6. The system according to claim 1 , wherein the portion defines a plurality of micro-openings. 7. The system according to claim 1 , further comprising a pressure control system in communication with the dispensing chamber. 8. A system for crystallization, comprising: at least one receiving member comprising a first electrically conductive member; at least one dispensing member comprising a second electrically conductive member; wherein the first and second electrical members are coupled in electrical communication; wherein the dispensing chamber and receiving chamber are separated by a porous membrane; whereby a complete electric circuit is obtained when electrolytes are present in the receiving and dispensing members. 9. A method for crystallizing a compound, the method comprising: providing a solution of a compound in at least one receiving member comprising a first electrically conductive member; providing a solution of a precipitate in at least one dispensing member comprising a second electrically conductive member; wherein the receiving and dispensing electrical members are coupled in electrical communication; and applying an electric field sufficient to controllably introduce the solution of precipitant into the solution of compound, wherein the applying an electric field comprises applying a first electric field sufficient to induce a nucleation of the compound at the one or more openings of the second receptacle, and applying a second electric field following nucleation, wherein the second electric field controls growth of the crystal. 10. The method of claim 9 , wherein the second electric field is different from the first electric field. 11. The method of claim 9 , wherein the first electric field is voltage-clamped (constant DC potential) or voltage-ramped; or the first electric field is current-clamped (constant current) or current-ramped; or the first electric field is a multi-segment combined DC-AC potential including a constant, pulsed and/or ramped waveform. 12. The method of claim 9 , wherein the second electric field is current-clamped or current ramped; or the second electric field is voltage-clamped or voltage ramped; or the second electric field is a multi-segment combined DC-AC potential including a constant and ramped waveform. 13. The method of claim 9 , wherein the first electric field is applied with oscillations at controlled/programmed amplitude and frequency. 14. The method of claim 9 , wherein the second electric field is applied with oscillations at controlled/programmed amplitude and frequency. 15. The method according to claim 11 , wherein the first electric field is a pulsed waveform comprising a triangular waveform, an AC sine, or a square wave. 16. The method of claim 9 , wherein the compound comprises a small molecule drug. 17. The method of claim 9 , wherein the compound comprises a peptide. 18. The method of claim 9 , wherein the compound comprises a protein. 19. The method of claim 9 , wherein the compound comprises a nucleic acid. 20. The method of claim 9 , wherein the compound comprises a complex. 21. The method of claim 9 , wherein the compound solution is a saturated solution, near saturated solution or super-saturated solution. 22. The method of claim 9 , wherein the precipitant comprises an anti-solvent. 23. The method of claim 9 , wherein the precipitant comprises an acid. 24. The method of claim 9 , wherein the precipitant comprises a base. 25. The method of claim 9 , wherein the precipitant comprises a precipitating reagent.
using electric fields, e.g. electrolysis · CPC title
Macromolecular compounds · CPC title
Control or regulation (control per se G05) · CPC title
by electrolysis · CPC title
Single-crystal growth from solutions using solvents which are liquid at normal temperature, e.g. aqueous solutions (from molten solvents C30B9/00; by normal or gradient freezing C30B11/00; under a protective fluid C30B27/00) · CPC title
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