The Application Notebook
Restek Corporation
Pain management LC analyses can be difficult to optimize because of the limited selectivity of C18 and phenyl-hexyl phases. In contrast, the selectivity of Raptor™ Biphenyl superficially porous particle (SPP) LC columns provides complete resolution of isobaric pain medications with a total cycle time of 5 min.
Accurate, reliable analysis of pain medications is a key component in monitoring appropriate medical use and preventing drug diversion and abuse. As the demand for fast, multicomponent methods grows, LC–MS–MS methods are increasingly desired for pain management and therapeutic drug monitoring because of the low detection limits that can be achieved with this highly sensitive and selective technique. However, despite the selectivity offered by mass spectrometry (MS), hydrophilic matrix components can still interfere with early-eluting drug compounds resulting in ion suppression. In addition, isobaric pairs must be chromatographically separated for positive identification. The need for highly selective and accurate methods makes LC column selection critical.
Table 1: Mobile phase gradient.
While C18 and phenyl-hexyl phases are frequently used for bioanalytical LC–MS–MS applications, Restek's Biphenyl phase offers better aromatic retention and selectivity for pharmaceutical and drug-like compounds, giving it a significant advantage over other phases for the analysis of pain management medications or other drugs of abuse. The Biphenyl phase, originally developed a decade ago by Restek, has recently been combined with Raptor™ SPP ("core–shell") silica particles to allow for faster separations without the need for expensive UHPLC instrumentation. Here, we demonstrate the fast, selective separation of commonly tested pain drugs that can be achieved using the new Raptor™ SPP Biphenyl LC column.
Table 2: Analyte retention times and transitions.
A standard containing multiple pain management drugs was prepared in blank human urine and diluted with mobile phase as follows, urine:mobile phase A:mobile phase B (17:76:7). The final concentration for all analytes was 10 ng/mL except for lorazepam, which was 100 ng/mL. Samples were then analyzed by LC–MS–MS using an AB SCIEX API 4000™ MS-MS in ESI+ mode. Chromatographic conditions, retention times, and mass transitions are presented here and in Tables 1 and 2:
Column: Raptor™ Biphenyl, 50 mm × 3.0 mm i.d. × 2.7 μm
Sample: Fortified urine
Inj. vol.: 10 μL
Inj. temp.: 30 °C
Mobile phase A: Water + 0.1% formic acid
Mobile phase B: Methanol + 0.1% formic acid
As shown in Figure 1, 18 commonly tested pain management drugs were analyzed, with the last compound eluting in less than 3.5 min, giving a total cycle time of 5 min on Restek's Raptor™ SPP Biphenyl LC column. Analyte retention times are presented in Table 2. Important isobaric pairs (morphine/hydromorphone and codeine/hydrocodone) were completely resolved and eluted as symmetrical peaks, allowing accurate identification and integration. In addition, early-eluting compounds such as morphine, oxymorphone, and hydromorphone are separated from hydrophilic matrix interferences, resulting in decreased ion-suppression and increased sensitivity. Similar analyses on C18 and phenyl-hexyl columns often exhibit poor peak shape and resolution (for example, peak tailing between closely eluting isobars), which makes identification and accurate quantification more difficult.
Figure 1: Baseline resolution of isobaric pain management drugs in sub-5-min runs on the Raptor⢠Biphenyl column.
Complete separation of critical pain management drug analytes from hydrophilic matrix components and isobaric interferences was achieved using the new Raptor™ SPP Biphenyl LC column in less than 5 min. The fast, complete separations produced in this method allow accurate quantification of pain management drugs and support increased sample throughput and improved lab productivity.
To learn more, visit www.restek.com/raptor
Restek Corporation
110 Benner Circle, Bellefonte, Pennsylvania 16823, USA
Tel: (800) 356 1688 fax: (814) 353 1309
Website: www.restek.com/raptor
HPLC 2025 Preview: The Present and Future of Automation in Analytical Laboratories
May 22nd 2025Analytical laboratories are undergoing a fundamental transformation. In the face of increasing sample volumes, growing regulatory requirements, and the rising demand for faster, more precise, and cost-efficient analysis, optimizing laboratory processes is becoming a central focus. Automation technologies offer promising solutions in this regard. Recently, they have evolved from isolated solutions to comprehensive systems that permeate nearly all areas of laboratory practice. This development not only opens up new opportunities in terms of efficiency, data quality, and scalability but also brings technical, organizational, and personnel challenges. To successfully address these, strategic approaches are needed that consider both the technological and human dimensions of the transformation.
Quantifying Isavuconazole in Dried Blood Spots Using HPLC
May 21st 2025Isavuconazole, an antimycotic agent used to treat fungal infections, can typically be found during dried blood spot sampling. However, there are obstacles that keep it from being an ideal approach for properly determining the drug’s presence.
Separating and Quantifying Spinach Flavonoids with UHPLC–MS/MS
May 21st 2025Researchers at Baylor College of Medicine’s Children's Nutrition Research Center (Houston, Texas) developed and validated a high-throughput extraction and ultrahigh-performance liquid chromatography–tandem mass spectrometry (UHPLC–MS/MS) method to separate and quantify 39 spinach flavonoid species in 11.5 min.