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1 ble, 18.4 h oral t(1/2), and 0.19 L/(h x kg) plasma clearance).
2 Primary outcome was measured GFR (iohexol plasma clearance).
3 adrenaline concentrations because of reduced plasma clearance.
4 acterized by high brain penetrance and rapid plasma clearance.
5 ral dosing, but exposure was limited by high plasma clearance.
6 docytosis of circulating LDL, increasing its plasma clearance.
7 properties but has poor solubility and rapid plasma clearance.
8 lipoproteins accumulate because of impaired plasma clearance.
9 GC 945 to KB tumor-bearing mice showed rapid plasma clearance (0.021 L/h) and tissue distribution.
10 iltration rateiohexol measured using iohexol plasma clearance: 19 2 vs 16 2 mL/min/1.73 m2; p = 0.13
11 half-life of disposition 69.7 +/- 39.7 hrs, plasma clearance 2.39 +/- 1.32 mL/hr/kg, and volume of d
12 f BPS, in comparison with BPA, and its lower plasma clearance (3.5 times lower), the oral BPS systemi
13 he liver was the major organ responsible for plasma clearance, accounting for >60% of the peptide upt
14 e drug-to-antibody ratio (DAR); however, ADC plasma clearance also increases with DAR, reducing expos
15 ient) were 10.8% and 0.88, respectively, for plasma clearance and 15.3% and 0.77, respectively, for f
17 higher plasma free fraction, and (c) faster plasma clearance and brain uptake kinetics, enabling mea
18 the C15 and C18 analogues displaying delayed plasma clearance and enhanced tumor uptake and retention
19 A, which in experimental models has a slower plasma clearance and greater fibrin specificity and is 8
20 receptor-related protein function, decreased plasma clearance and hepatic uptake of (131)I-apoB-48 LD
22 ptor class B (SR-BI) failed to normalize the plasma clearance and liver uptake of [(3)H]CE from LCAT-
23 roperties in the rat and dog with respect to plasma clearance and oral bioavailability and is a poten
26 f eliminating the MR on MR- and MPR-mediated plasma clearance and tissue distribution of infused phos
28 bind the replaced glycoprotein, increase its plasma clearance, and inhibit its activity, preventing s
29 umor model simulating the interstitial flow, plasma clearance, and transport of the drug within the t
30 nts were half-life, time to C(max) [t(max)], plasma clearance, and volume of distribution of cagrilin
33 ts provided excellent renal images, with the plasma clearance averaging 228 mL/min for (99m)Tc(CO)(3)
34 duced cocaine burden in tissues, accelerated plasma clearance by 20-fold, and prevented cocaine-induc
35 rformed to quantify manganese and gadolinium plasma clearance by using inductively coupled plasma mas
36 mple at 45 min was found to be 23, using the plasma clearance calculated from a multi-sample clearanc
37 51)Cr-ethylenediaminetetraacetic acid (EDTA) plasma clearance counting but is time-consuming and requ
38 (99m)Tc-Diethylenetriaminepentaacetic acid plasma clearance curves from 79 subjects were analyzed.
39 We evaluated this approach for interpreting plasma clearance curves with the goal of reducing curve-
40 by applying a three-compartment model to the plasma clearance data of intravenously injected [(14)C]i
42 ts show that these three compounds exhibit a plasma clearance equivalent to iothalamate (a commonly c
43 Results indicated that drug lipophilicity, plasma clearance, faster target dissociation, and, in pa
52 based formulas with a gold standard (iohexol plasma clearance) in 193 renal transplant recipients usi
53 ; measurements of (14)C-ACPC and (67)Ga-DTPA plasma clearance (K(1)), (14)C-ACPC transport ( partial
54 hods of measuring whole-skeleton (99m)Tc-MDP plasma clearance (K(bone)) in 12 osteoporotic postmenopa
56 n volunteers followed by sequential imaging, plasma clearance measurements and timed urine collection
58 GFR measured by nonradiolabeled iothalamate plasma clearance (mGFR) in 72 subjects with cirrhosis.
59 using the slope-intercept method for iohexol plasma clearance (mGFR) in population cohorts from Malaw
61 s for mGFR determination using 1-compartment plasma clearance models and iohexol as the exogenous fil
63 uterium-labeled steroid hormones as tracers; plasma clearance of 100 mg of hydrocortisone; levels of
64 ce, capture ELISA measurements revealed fast plasma clearance of 11C7-scFv8D3 concomitantly with brai
65 se complexes (alpha 2M*) also diminished the plasma clearance of 125I-factor Xa in a dose-dependent f
71 4 years' follow-up we estimated GFR from the plasma clearance of 51Cr-labelled edetic acid (EDTA), an
72 nomolar affinity to TSLP (K(D) = 13 nM), low plasma clearance of 6.4 mL/min/kg, and an effective half
80 urement of glomerular filtration rate by the plasma clearance of an IV single dose of iohexol and est
81 en together, these data showed that impaired plasma clearance of apoE2-containing, triglyceride-rich
82 in the liver responsible for the binding and plasma clearance of apolipoprotein E-containing lipoprot
83 explained between-individual variability in plasma clearance of bedaquiline, its M2 metabolite, and
84 r both before and after I/R and improved the plasma clearance of bile acid and biliary outputs of bil
86 ignificant correlations between CrCl and the plasma clearance of both total topotecan [Spearman's cor
90 imum observed plasma concentration and total plasma clearance of ET-743 (mean +/- standard deviation)
91 ethods for GFR measurement using urinary and plasma clearance of exogenous filtration markers and foc
96 synthesized VLDL normally but showed reduced plasma clearance of human VLDL and a corresponding reduc
98 ocus on urinary clearance of iothalamate and plasma clearance of iohexol compared with inulin clearan
99 dults referred for measured GFR (mGFR) using plasma clearance of iohexol in Stockholm, Sweden, who ha
101 filtration rate (determined by measuring the plasma clearance of iohexol) between the baseline value
103 erious disorder caused by very low or absent plasma clearance of LDL, substantially raised LDL choles
104 PS, whereas SR-BI-null mice showed decreased plasma clearance of LPS into the liver and hepatocytes c
115 ntrast to the situation observed in baboons, plasma clearances of both compounds were similar in huma
117 area under the curve (0-last) and decreased plasma clearance over compound I and efavirenz, the stan
118 and desialylated pFn (aFn) displayed a rapid plasma clearance (P < .001) with greater than 50% of bot
119 ution of ADC, independent of payload dose or plasma clearance, plays a major role in ADC efficacy.Sig
121 amine sulfoconjugated to the respective free plasma clearances (r2 = .30, p < .01, and r2 = 0.29, p <
122 the natural logarithm of the respective free plasma clearances (r2 = 0.58, p < .001, and r2 = 0.39, p
123 lus and the Thiele modulus are ratios of the plasma clearance rate and antibody catabolism, respectiv
124 On a time scale of minutes, we determine the plasma clearance rate in the wild-type mouse, using time
129 ion within a tumor including dose, affinity, plasma clearance, target expression, internalization, pe
132 es were about 21.1 and 3.4 times slower than plasma clearance times for nalmefene and naloxone, respe
135 ts, which was commensurate with the observed plasma clearance values upon intravenous administration.
136 result in a 2-5-fold increase in calculated plasma clearance values when the excipient interferes wi
137 netic experiments, four trioxolanes had high plasma clearance values, suggesting a potential metaboli
138 curve increased linearly with dose, and mean plasma clearance was 1.86 mL/kg/min (range, 1.21 to 2.41
139 controls -(5.3 +/- 1.7) x 10(-3) s(-1), and plasma clearance was 2.6-fold higher in BCC than control
146 ter iv ddI administration, only the maternal plasma clearance was found to be significantly increased
147 ined in a biexponential manner, and systemic plasma clearance was high relative to liver blood flow.
150 osed mice; however, in the pre-dosed animals plasma clearance was more rapid and tissue clearance app
155 examethasone drug conjugate exhibited a fast plasma clearance, with a half-life of approximately 5-8