Methods to increase sensitivity of LC/MS analysis
View Patent ↗The present disclosure discusses a method of separating a sample (e.g., pharmaceutical drug, genotoxic impurity, biomarker, and/or biological metabolite) including coating a metallic flow path of a chromatographic system; injecting the sample into the chromatographic system; flowing the sample through the chromatographic system; separating the sample; and analyzing the separated sample using mass spectroscopy. In some examples, the coating applied to the surfaces defining the flow path is non-binding with respect to the sample—and the separated sample. Consequently, the sample does not bind to the low-binding surface of the coating of the flow path. The applied coating can increase the chromatographic peak area for the sample of the chromatographic system.
1. A method of separating and analyzing a metal sensitive sample comprising:
providing a chromatographic system having an alkylsilyl surface coating;
injecting the sample into the chromatographic system, wherein the sample comprises one or more compounds having a sulfur dioxide constituent;
flowing the sample through the chromatographic system; and
separating the sample, wherein coating the metallic flow path of the chromatographic system increases a chromatographic peak area of the compounds in the sample of at least 1.6× in comparison to an uncoated chromatographic system having metallic surfaces exposed to fluids.
2. The method of claim 1 , wherein the sample does not bind to the coating of the metallic flow path.
3. The method of claim 1 , wherein the one or more of the compounds are diazoxide and/or bicalutamide.
4. The method of claim 1 , wherein providing a chromatographic system comprises: assessing a polarity of a compound in the sample; selecting a desired contact angle and coating material based on polarity assessment; coating a metallic flow path of the chromatographic system with an alkylsilyl surface coating, and adjusting hydrophobicity of the flow path by vapor deposition of an alkylsilyl.
5. The method of claim 1 , wherein the alkylsilyl surface coating comprises bis(trichlorosilyl)ethane or bis(trimethoxysilyl)ethane.
6. A method of separating a sample comprising:
providing a chromatographic system having a metallic flow path with an alkylsilyl coating on fluid exposed surfaces, the metallic flow path with the alkylsilyl coating preventing the sample from binding to underlying metal surfaces;
injecting the sample into the chromatographic system, wherein the sample comprises one or more compounds having hydroxyl and nitrogen moieties which are in a spatial arrangement that allows the hydroxyl and nitrogen moieties to form chelates with metals;
flowing the sample through the chromatographic system; and
separating the sample, wherein coating the metallic flow path of the chromatographic system increases a chromatographic peak area of the compounds in the sample of at least 1.6× in comparison to an uncoated chromatographic system having metallic surfaces exposed to fluids.
7. The method of claim 6 , wherein the chromatographic system comprises a mix-mode chromatographic column.
8. The method of claim 6 , wherein the chromatographic system comprises a phenyl-hexyl chromatographic column.
9. The method of claim 6 , wherein the alkylsilyl coating comprises bis(trichlorosilyl)ethane or bis(trimethoxysilyl)ethane.
10. The method of claim 6 , wherein one or more of the compounds are selected from the group consisting of salmeterol, apomorphine, and dobutamide.
11. A method of separating a sample comprising:
providing a chromatographic system having a metallic flow path with an alkylsilyl coating on fluid exposed surfaces, the metallic flow path with the alkylsilyl coating preventing the sample from binding to underlying metal surfaces;
injecting the sample into the chromatographic system, wherein the sample comprises N-nitrosodimethylamine (NDMA) and/or N-nitrosodiethylamine (NDEA);
flowing the sample through the chromatographic system; and
separating the sample, wherein coating the metallic flow path of the chromatographic system increases a chromatographic peak area of the NDMA and NDEA in a sample of at least 1.4× in comparison to an uncoated chromatographic system having metallic surfaces exposed to fluids.
12. The method of claim 11 , wherein the chromatographic system comprises a mix-mode chromatographic column.
13. The method of claim 11 , wherein the chromatographic system comprises a phenyl-hexyl chromatographic column.
14. The method of claim 11 , wherein the alkylsilyl coating comprises bis(trichlorosilyl)ethane or bis(trimethoxysilyl)ethane.