Table 3.
Concordance of results obtained using the Exactive-MS method and LC-MS/MS methods for analysis of plasma samples from a clinical trial.
| Analyte | LOI by LC-MS/MS (ng/ml) | LOI by Exactive-MS (ng/ml) | Positive by LC-MS/MS Only (n) | Positive by Exactive-MS Only (n) | Positive by Exactive-MS and LC-MS/MS (n) | Negative by Exactive-MS and LC-MS/MS (n) | Concordance (Percent Agreement, %) |
|---|---|---|---|---|---|---|---|
| Protease Inhibitors (PIs) | |||||||
| Ataznavir | 100 | 5 | 0 | 0 | 5 | 59 | 100 |
| Ritonavir | 100 | 5 | 0 | 1 | 2 | 61 | 98.4 |
| Nucleotide/Nucleoside Reverse Transcriptase Inhibitors (NRTIs) | |||||||
| Emtricitabine | 5 | 10 | 0 | 0 | 11 | 53 | 100 |
| Lamivudine | 20 | 5 | 2 | 0 | 26 | 36 | 96.8 |
| Tenofovir | 5 | 10 | 0 | 1 | 9 | 54 | 98.4 |
| Zidovudine | 5 | 10b | 6 | 1 | 8 | 49 | 89.1 |
| Non-Nucleotide/Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) | |||||||
| Efavirenz | 100 | 150 | 0 | 0 | 13 | 51 | 100 |
| Nevirapine | 20 | 5 | 2 | 1 | 15 | 46 | 95.3 |
| Analyte | LOI by LC-MS/MS (ng/ml) | LOI by Exactive-MS (ng/ml) | Positive by LC-MS/MS Only (n) | Positive by Exactive-MS Only (n) | Positive by Exactive-MS and LC-MS/MS (n) | Negative by Exactive-MS and LC-MS/MS (n) | Concordance (Percent Agreement, %) |
|---|---|---|---|---|---|---|---|
| Protease Inhibitors (PIs) | |||||||
| Ataznavir | 100 | 5 | 0 | 0 | 5 | 59 | 100 |
| Ritonavir | 100 | 5 | 0 | 1 | 2 | 61 | 98.4 |
| Nucleotide/Nucleoside Reverse Transcriptase Inhibitors (NRTIs) | |||||||
| Emtricitabine | 5 | 10 | 0 | 0 | 11 | 53 | 100 |
| Lamivudine | 20 | 5 | 2 | 0 | 26 | 36 | 96.8 |
| Tenofovir | 5 | 10 | 0 | 1 | 9 | 54 | 98.4 |
| Zidovudine | 5 | 10b | 6 | 1 | 8 | 49 | 89.1 |
| Non-Nucleotide/Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) | |||||||
| Efavirenz | 100 | 150 | 0 | 0 | 13 | 51 | 100 |
| Nevirapine | 20 | 5 | 2 | 1 | 15 | 46 | 95.3 |
| Analyte | LOI by LC-MS/MS (ng/ml) | LOI by Exactive-MS (ng/ml) | Positive by LC-MS/MS Only (n) | Positive by Exactive-MS Only (n) | Positive by Exactive-MS and LC-MS/MS (n) | Negative by Exactive-MS and LC-MS/MS (n) | Concordance (Percent Agreement, %) |
|---|---|---|---|---|---|---|---|
| Protease Inhibitors (PIs) | |||||||
| Ataznavir | 100 | 5 | 0 | 0 | 5 | 59 | 100 |
| Ritonavir | 100 | 5 | 0 | 1 | 2 | 61 | 98.4 |
| Nucleotide/Nucleoside Reverse Transcriptase Inhibitors (NRTIs) | |||||||
| Emtricitabine | 5 | 10 | 0 | 0 | 11 | 53 | 100 |
| Lamivudine | 20 | 5 | 2 | 0 | 26 | 36 | 96.8 |
| Tenofovir | 5 | 10 | 0 | 1 | 9 | 54 | 98.4 |
| Zidovudine | 5 | 10b | 6 | 1 | 8 | 49 | 89.1 |
| Non-Nucleotide/Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) | |||||||
| Efavirenz | 100 | 150 | 0 | 0 | 13 | 51 | 100 |
| Nevirapine | 20 | 5 | 2 | 1 | 15 | 46 | 95.3 |
a. The LC-MS/MS method included an isotopically-labeled internal standard for zidovudine and monitors fragments at a limit of identification of 5 ng/ml. The full scan-HRMS does not monitor fragments < 50 ng/ml.
The LC-MS/MS method included an isotopically-labeled internal standard for zidovudine and monitors fragments at a limit of identification of 5 ng/ml. The full scan-HRMS does not monitor fragments < 50 ng/ml.
a. The LC-MS/MS method included an isotopically-labeled internal standard for zidovudine and monitors fragments at a limit of identification of 5 ng/ml. The full scan-HRMS does not monitor fragments <50 ng/ml.