词条 | Push–pull perfusion |
释义 |
this technique replaced the cortical cup technique for observing neurotransmitters. The advent of concentric microdialysis probes in the 1980s resulted in push-pull sampling falling out of favor, as such probes require less monitoring, and are less invasive than the higher flow rate push-pull probes (>10 microliter/min), which could result in lesions if flow is unbalanced.[2] With the advent of microfluidics and miniaturized probes, low-flow push–pull sampling was developed in 2002.[3] By using flow rates of ~50 nL/min, this technique minimizes tissue damage while providing finer spatial resolution than microdialysis sampling. References1. ^{{cite journal|last=Gaddum|first=J.H.|title=Push-pull cannulae|journal=Journal of Physiology|year=1961|volume=155|issue=1|pages=1P–2P}} 2. ^{{cite journal|last=Myers|first=R.D.|author2=Adell, A. |author3=Lankford, M.F. |title=Simultaneous comparison of cerebral dialysis and push-pull perfusion in the brain of rats: a critical review|journal=Neuroscience & Biobehavioral Reviews|year=1998|volume=22|issue=3|pages=371–387|doi=10.1016/S0149-7634(97)00025-0 }} 3. ^{{cite journal|last=Kottegoda|first=Sumith|author2=Shaik, Imtiazuddin |author3=Shippy, Scott A. |title=Demonstration of low flow push-pull perfusion|journal=Journal of Neuroscience Methods|year=2002|volume=121|issue=1|pages=93–101|doi=10.1016/S0165-0270(02)00245-5|pmid=12393165 }} External links
3 : Biochemistry methods|Neurochemistry|Neurotechnology |
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