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1 0.08 times at low filtration rates (4 g l-1 infusates).
2 the primate right frontal lobe or pons with infusate.
3 (50 microM) was added to the 100 mM glucose infusate.
4 f HA2000 increased substantially relative to infusate and the subsynovial and lymph concentrations fe
5 sources (skin, catheter segments, hubs, and infusate) and confirmed by restriction-fragment DNA subt
6 es at intermediate filtration rates (2 g l-1 infusates) and 1.26 +/- 0.08 times at low filtration rat
7 s were performed using Evans blue dye as the infusate, and interstitial fluid pressure was measured.
8 ml(-1) (mean +/-s.e.m., n= 31), exceeded the infusate concentration, 0.20 mg ml(-1), while subsynovia
11 esponses, along with luminal distribution of infusate during esophageal rapid and slow infusion of ai
14 04 times at high filtration rates (0.2 g l-1 infusates; mean +/- S.E.M.), 1.60 +/- 0.09 times at inte
19 , and proper preparation of local anesthetic infusate solutions are all considered essential componen
21 erum sodium concentration over 200 min or an infusate that maintained serum sodium concentration.
22 ugh further dose escalation was precluded by infusate volume constraints, this SU101 dose schedule re
23 sertion (infusion of peripherally compatible infusates vs. vesicants), and duration of use (</=5 days
27 ion of platelet-like particles (PLPs) in the infusate, which include platelets released during ex viv
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