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Signaling lipid profiling offers critical insights into human health by revealing the molecular drivers of inflammation, metabolic disorders, and cancer. While traditional blood collection remains the gold standard, it requires invasive venous access and strict cold-chain logistics. Volumetric absorptive microsampling (VAMS) has emerged as a promising alternative, enabling precise, low-volume sampling. Recent comparative analyses demonstrate that VAMS provides distinct advantages over conventional whole blood (WB) and dried blood spot (DBS) methods, particularly regarding precision and short-term stability.
Researchers evaluated the analytical performance of VAMS using a single liquid-liquid extraction (LLE) protocol. The study compared precision, recovery, and matrix effects across various sampling platforms. Results indicated that VAMS achieves superior precision when compared to DBS. Furthermore, the metabolic profile of VAMS samples closely aligns with those obtained from fresh whole blood. In contrast, DBS often shows substantial metabolic deviation, which may complicate clinical interpretations during routine monitoring.
Lipid stability remains a primary concern in bioanalytical research. The study showed that VAMS maintains improved lipid stability during the initial 24 hours at room temperature. However, clinicians and researchers must exercise caution with extended storage. When storage exceeded one week, significant artifacts appeared in the samples due to hydrolytic and oxidative degradation. Consequently, implementing stabilization strategies is essential for high-quality signaling lipid profiling. Experts recommend using desiccant-assisted storage or antioxidant pretreatment to preserve the integrity of low-abundance lipid species over longer periods.
The transition toward decentralized clinical trials and remote monitoring in India necessitates reliable microsampling techniques. While VAMS shows great potential, further optimization of extraction efficiency from the tip is required. Advancing these protocols will facilitate the broader application of lipidomics in personalized medicine and routine diagnostics. Specifically, addressing long-term stability will be the next critical step for global implementation.
VAMS provides higher analytical precision and more closely reflects the metabolic profile of fresh whole blood compared to traditional dried blood spots.
VAMS samples demonstrate improved lipid stability during the first 24 hours at room temperature, making them suitable for rapid transport without immediate freezing.
Researchers suggest using desiccant-assisted storage or pretreating the tips with antioxidants to prevent oxidative and hydrolytic breakdown of signaling lipids.
Disclaimer: This content is for informational and educational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional for diagnosis and treatment. Refer to the latest local and national guidelines for clinical practice.
References
Thangavelu MU et al. Volumetric absorptive microsampling for profiling of signaling lipids: a comparative analysis with whole blood and dried blood spots. Anal Bioanal Chem. 2026 Apr 05. doi: 10.1007/s00216-026-06413-5. PMID: 41936005.
Chalfant CE. Lipidomics in translational research and the clinical significance of lipid-based biomarkers. Transl Res. 2017 Nov;189:1-11. doi: 10.1016/j.trsl.2017.06.006. PMID: 28668521.
Volani C et al. Volumetric Absorptive Microsampling of Blood for Untargeted Lipidomics. Molecules. 2021 Jan 7;26(2):262. doi: 10.3390/molecules26020262. PMID: 33430335.
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A comparative study shows VAMS offers better precision and 24-hour stability than DBS for profiling signaling lipids, supporting its use in clinical lipidom...
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