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Negligible In Vitro Recovery of Macromolecules from Microdialysis Using 100 kDa Probes and Dextran in Perfusion Fluid

Overview
Journal Neurochem Res
Specialties Chemistry
Neurology
Date 2024 Mar 13
PMID 38478218
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Abstract

Microdialysis is applied in neurointensive care to monitor cerebral glucose metabolism. If recoverable, macromolecules may also serve as biomarkers in brain disease and provide clues to their passage across the blood-brain barrier. Our study aimed to investigate the in vitro recovery of human micro- and macromolecules using microdialysis catheters and perfusion fluids approved for clinical use. In vitro microdialysis of a bulk solution containing physiological or supraphysiological concentrations of glucose, lactate, pyruvate, human IgG, serum albumin, and hemoglobin was performed using two different catheters and perfusion fluids. One had a membrane cut-off of 20 kDa and was used with a standard CNS perfusion fluid, and the other had a membrane cut-off of 100 kDa and was perfused with the same solution supplemented with dextran. The flow rate was 0.3 µl/min. We used both push and push-pull methods. Dialysate samples were collected at 2-h intervals for 6 h and analyzed for relative recovery of each substance. The mean relative recovery of glucose, pyruvate, and lactate was > 90% in all but two sets of experiments. In contrast, the relative recovery of human IgG, serum albumin, and hemoglobin from both bulk solutions was below the lower limit of quantification (LLOQ). Using a push-pull method, recovery of human IgG, serum albumin, and hemoglobin from a bulk solution with supraphysiological concentrations were above LLOQ but with low relative recovery (range 0.9%-1.6%). In summary, exchanging the microdialysis setup from a 20 kDa catheter with a standard perfusion fluid for a 100 kDa catheter with a perfusion solution containing dextran did not affect the relative recovery of glucose and its metabolites. However, it did not result in any useful recovery of the investigated macromolecules at physiological levels, either with or without a push-pull pump system.

References
1.
Hillered L, Persson L, Nilsson P, Ronne-Engstrom E, Enblad P . Continuous monitoring of cerebral metabolism in traumatic brain injury: a focus on cerebral microdialysis. Curr Opin Crit Care. 2006; 12(2):112-8. DOI: 10.1097/01.ccx.0000216576.11439.df. View

2.
Lindblad C, Raj R, Zeiler F, Thelin E . Current state of high-fidelity multimodal monitoring in traumatic brain injury. Acta Neurochir (Wien). 2022; 164(12):3091-3100. PMC: 9705453. DOI: 10.1007/s00701-022-05383-8. View

3.
Bungay P, Wang T, Yang H, Elmquist W . Utilizing transmembrane convection to enhance solute sampling and delivery by microdialysis: theory and in vitro validation. J Memb Sci. 2010; 348(1-2):131-149. PMC: 2802079. DOI: 10.1016/j.memsci.2009.10.050. View

4.
Guilfoyle M, Helmy A, Donnelly J, Stovell M, Timofeev I, Pickard J . Characterising the dynamics of cerebral metabolic dysfunction following traumatic brain injury: A microdialysis study in 619 patients. PLoS One. 2021; 16(12):e0260291. PMC: 8675704. DOI: 10.1371/journal.pone.0260291. View

5.
Yang D, Tsai T, Cheng C, Lee C, Chen S, Cheng F . Simultaneous monitoring of extracellular glucose, pyruvate, lactate and glutamate in gerbil cortex during focal cerebral ischemia by dual probe microdialysis. J Chromatogr A. 2001; 913(1-2):349-54. DOI: 10.1016/s0021-9673(00)01033-5. View