Method and system for metastasis diagnosis and prognosis
US-2018100849-A1 · Apr 12, 2018 · US
US10137480B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10137480-B2 |
| Application number | US-201615387591-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 21, 2016 |
| Priority date | Mar 26, 2015 |
| Publication date | Nov 27, 2018 |
| Grant date | Nov 27, 2018 |
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A method of treating a sensor array including a plurality of sensors and an isolation structure, where a sensor of the plurality of sensors has a sensor pad exposed at a surface of the sensor array and the isolation structure is disposed between the sensor pad and sensor pads of other sensors of the plurality of sensors, comprises exposing the sensor pad and the isolation structure to a non-aqueous organo-silicon solution including an organo-silicon compound and a first non-aqueous carrier; applying an acid solution including an organic acid and a second non-aqueous carrier to the sensor pad; and rinsing the acid solution from the sensor pad and the isolation structure.
Opening claim text (preview).
What is claimed is: 1. A method of treating a sensor array, the sensor array including a plurality of sensors and an isolation structure, a sensor of the plurality of sensors having a sensor pad exposed at a surface of the sensor array, wherein the exposed surface of the sensor pad defines a bottom surface of the isolation structure, the method comprising: exposing the exposed surface of the sensor pad to a non-aqueous organo-silicon solution including an organo-silicon compound and a first non-aqueous carrier; applying an acid solution including an organic acid and a second non-aqueous carrier to the exposed surface of the sensor pad; and rinsing the acid solution from the exposed surface of the sensor pad. 2. The method of claim 1 , wherein a portion of the organo-silicon compound remains on the isolation structure. 3. The method of claim 1 , wherein the organo-silicon compound includes a silane functionalized with an aryl, polyaryl, alkyl, alkoxy, halo, or cyano moiety, or any combination thereof. 4. The method of claim 1 , wherein the organo-silicon compound includes a polysiloxane including aryl, dialkyl or alkylhydro units, or combinations thereof. 5. The method of claim 1 , wherein the organo-silicon compound includes a polysiloxane including hydrophilic, polar, or amphiphilic units, or combinations thereof. 6. The method of claim 1 , wherein the organo-silicon compound includes a silazane. 7. The method of claim 1 , wherein the organo-silicon compound has a molecular weight in a range of 50 Da to 10000 Da. 8. The method of claim 1 , wherein the non-aqueous organo-silicon solution includes the organo-silicon compound in an amount of 0.001% to 10.0% by weight. 9. The method of claim 1 , wherein the organic acid includes sulfonic acid. 10. The method of claim 1 , wherein the first non-aqueous carrier is an alkane having between 6 and 24 carbons. 11. The method of claim 1 , further comprising heating the sensor pad and the non-aqueous organo-silicon solution while exposing the sensor pad to the non-aqueous organo-silicon solution. 12. The method of claim 1 , further comprising exposing at least the sensor pad to a basic solution. 13. The method of claim 3 , wherein the silane is selected from the group consisting of phenyldimethylchlorosilane, tert-butylchlorodiiphenylsilane, chlorotripropylsilane, (N,N-dimethylamino) trimethyl-silane, tris(trimethylsilyl)silane, triethylchlorosilane, 3-cyanopropyldimethylchloro-silane, chlorotriethylsilane, 1,2-bis(chlorodimethylsiyl)ethane, trimethylsilyltrifluoronesulfonate, trioctylsilane, dodecyldimethylchlorosilane, chlorodimethylthexylsilane, trimethylchlorosilane, chloro(chloromethyl) dimethylsilane, thexyldimethylchlorosilane, triisopropylchlorosilane, trimethylmethoxysilane, trimethylchlorosilane, chlorotriisopropylsilane, acetoxytrimethylsilane, and a combination thereof. 14. The method of claim 4 , wherein the aryl unit includes a phenylalkyl siloxyl unit. 15. The method of claim 4 , wherein the dialkyl unit or the alkylhydro unit includes an alkyl moiety selected from methyl, ethyl, propyl, butyl moieties, and a combination thereof. 16. The method of claim 9 , wherein the sulfonic acid includes dodecyl benzene sulfonic acid. 17. The method of claim 12 , wherein the basic solution includes between 0.005M and 1.5M sodium hydroxide. 18. The method of claim 15 , wherein the polysiloxane includes a siloxane selected from the group consisting of an alkyl terminated polydimethylsiloxane, a hydride-terminated polydimethylsiloxane, a monovinyl terminated polydimethylsiloxane, dichloro-tetramethyldisiloxane, hexamethyltrisiloxane, polymethylhydrosiloxane, tris(trimethylsilyloxy)silane, octamethyltrisiloxane, and a combination thereof.
Cleaning during device manufacture · CPC title
to obtain a coating with specific electrical properties · CPC title
Integrated circuits therefor, e.g. fabricated by CMOS processing · CPC title
derived from aromatic compounds · CPC title
Ion-sensitive or chemical field-effect transistors, i.e. ISFETS or CHEMFETS · CPC title
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