The HPLC-MS/MS system consisted of an Ultimate 3000 autosampler and pump with inline degasser, all of Dionex (Sunnyvale, CA, USA), connected to a degasser from LC Packings. The autosampler with a 100 μL sample loop was coupled to an AB Sciex API4000 mass spectrometer (Framingham, MA, USA) via a Shimadzu Prominence Column Oven (type CTO-20A) which was kept at 35 °C. Separation was performed with an Agilent column 2.1 × 100mm packed with material of Zorbax Extend 3.5 μm C-18 and kept at 35 °C using a CTO-20A column oven (Shimadzu, Kyoto, Japan). Instrument control and data acquisition was done using Analyst v1.6.2 and DCMS-link v2.12 software (Dionex).
Speedvac high capacity concentrator
The SpeedVac High Capacity Concentrator is a laboratory equipment designed to gently remove solvents and concentrate samples. It utilizes a vacuum system and controlled temperature to efficiently evaporate liquid samples, preserving the integrity of the sample materials.
3 protocols using speedvac high capacity concentrator
HPLC-MS/MS Analysis of Samples
The HPLC-MS/MS system consisted of an Ultimate 3000 autosampler and pump with inline degasser, all of Dionex (Sunnyvale, CA, USA), connected to a degasser from LC Packings. The autosampler with a 100 μL sample loop was coupled to an AB Sciex API4000 mass spectrometer (Framingham, MA, USA) via a Shimadzu Prominence Column Oven (type CTO-20A) which was kept at 35 °C. Separation was performed with an Agilent column 2.1 × 100mm packed with material of Zorbax Extend 3.5 μm C-18 and kept at 35 °C using a CTO-20A column oven (Shimadzu, Kyoto, Japan). Instrument control and data acquisition was done using Analyst v1.6.2 and DCMS-link v2.12 software (Dionex).
Oxytocin Radioimmunoassay Protocol
Saliva Oxytocin Extraction and Measurement
After evaporation using a SpeedVac High Capacity Concentrator (Thermo Scientific, Massachusetts, USA) 50 μl of assay buffer was added. The oxytocin was then measured with a highly sensitive and specific radio-immuno assay, standardized and validated in human studies. The detection limit was in the 0.5 pg/sample range, the intraassay variation was less than 8% and the < 0.7% cross reactivity was considered negligibly small.
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