Influence of radiopaque fillers on physicochemical properties of a model epoxy resin-based root canal sealer. (65/89)

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Investigation on the structure and upconversion fluorescence of Yb(3)(+)/Ho(3)(+) co-doped fluorapatite crystals for potential biomedical applications. (66/89)

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Passage of chromium-mordanted and rare earth-labeled fiber: time of dosing kinetics. (67/89)

Coastal bermudagrass hay was labeled with Cr by the Cr-mordant procedure and with 177Lu applied to the same fiber. Neutral detergent fiber prepared from the same Coastal bermudagrass hay was labeled with Yb, 169Yb, Tb and 160Tb by soaking overnight following by thorough washing and drying. Wood chips were similarly labeled with Sm or La, and Solka Floc was labeled with 147Nd and 141Ce. The carriers, labels and times of administration to cattle were: bermudagrass fiber with both Cr and 177Lu, bermudagrass fiber with 169Yb and Solka Floc labeled with 147Nd at 0 h; bermudagrass fiber with Yb, Solka Floc with 141Ce and wood chips with Sm at 24 h; wood chips with La at 48 h; and bermudagrass fiber labeled with 160Tb at the beginning and labeled with Tb at the end of a meal. Fecal collection followed and passage characteristics were determined with a two-compartment, age-dependent model. Markers labeling the different fiber sources had different (P less than .01) passage rates (Solka Floc greater than Coastal bermudagrass greater than wood chips), but there was no difference within fiber source for rare earth passage. There also was no difference between the passage characteristics of Cr-mordant and 177Lu. However, passage rate of particles administered at the beginning of the meal (160Tb) was 42% higher than for particles at the end of the meal (Tb).(ABSTRACT TRUNCATED AT 250 WORDS)  (+info)

Oncomodulin. 1H NMR and optical stopped-flow spectroscopic studies of its solution conformation and metal-binding properties. (68/89)

As deduced from its 1H NMR spectrum, oncomodulin's solution conformation is very similar to the tertiary structure of other single domain 2-site calcium-binding proteins of the troponin C class. Despite its extensive amino acid sequence homology with parvalbumins, however, oncomodulin differs significantly from these proteins in its Ca(II)----Ln(III) exchange characteristics. Although the relative affinity of Lu(III) for the EF site of Ca2-oncomodulin was normal, beta Lu:EF/beta Ca:EF being 175 +/- 15, displacement of Ca(II) from the CD site was not favored, beta Lu:CD/beta Ca:CD being 1.2 +/- 0.1. Lineshape analyses of several 1H NMR resonances generated by the Lu(III) titration of Ca2-oncomodulin indicated that Ca(II)----Ln(III) exchange at the CD site was 15-20 s-1, approximately 100 times faster than exchange at the CD site of parvalbumins. Analyses of the distribution of metal-bound oncomodulin species showed that Ca(II)----Lu(III) exchange was cooperative, the coefficient of cooperativity being estimated as 5 +/- 1. The kinetics of the release of Yb(III) from oncomodulin as measured by optical stopped-flow techniques corroborated the observed cooperativity in metal binding; the off-rate constant of Yb(III) from the EF site of Yb2-oncomodulin was 0.0036 s-1, approximately 19 times slower than the release of Yb(III) from the EF site of Ca1Yb1-oncomodulin. We attribute part of the reduced preference of small Ln(III)s for the CD site of oncomodulin to a combination of this site's inherent incompressibility (Williams, T.C., Corson, D.C. & Sykes, B.D. (1984) J. Am. Chem. Soc. 106, 5698-5702) and the Glu----Asp substitution at sequence position 59, the residue which chelates metal at the -X coordination position. Like the CD site in oncomodulin, site III in troponin C has not only a lower affinity for calcium relative to the CD site of parvalbumins but also aspartic acid at its -X position; a water molecule bridges the gap between bound metal and the carboxyl group of the relatively short side chain of Asp-114 (Herzberg, O. & James, M. N. G. (1985) Biochemistry 24, 5298-5302). Hence, we suggest that Asp-59 in oncomodulin binds metal only indirectly through an intervening water molecule, a proposal which is consistent with the CD site's reduced affinity for ions the size of Ca(II) or smaller.  (+info)

Evaluation of rare-earth markers using an in vitro ruminal fermentation system and effect of processing method on ruminal turnover of sized corn particles. (69/89)

A two-stage in vitro ruminal fermentation experiment was conducted to determine the extent of marker migration and the effects of marker addition on digestibility. Fermentation studies were terminated either at the end of stage I, the fermentation phase, or stage II, the pepsin digestion phase. Treatment diets contained ytterbium-marked corn plus chopped Coastal bermudagrass hay and nonmarked corn plus chopped hay. After stage I of the in vitro ruminal fermentation, 90% of ytterbium was recovered. Of this, 8.8% of the ytterbium had migrated to the hay, 2% was recovered in the supernatant and 89.2% remained bound to the corn. After completion of both stages, 72% was recovered, of which 7.9% was bound to corn, 33.6% was bound to the hay, 1.1% was recovered in the stage I supernatant and 57.4% was associated with the acid pepsin supernatant. Dry matter digestion was not affected after stage I but after stage II, digestibility was decreased 7% due to marker addition. A ruminal-cannulated Holstein steer weighing approximately 680 kg was used to determine turnover rates from the rumen of liquid and five different particle sizes of corn. Corn from each of two processing methods was fractionated into five particle sizes by dry-sieving. The corn particles included steam-rolled corn (SRC) retained on a 4-mm sieve and marked with dysprosium, SRC retained on a 2-mm sieve and marked with erbium, cracked corn (CC) retained on a 4-mm sieve and marked with yttrium, CC retained on a 2-mm sieve and marked with ytterbium, and CC retained on a 1-mm sieve and marked with samarium.(ABSTRACT TRUNCATED AT 250 WORDS)  (+info)

Measurement of glomerular filtration rate: single injection plasma clearance method without urine collection. (70/89)

Glomerular filtration rate (GFR) can be calculated from the plasma clearance of any of several radiopharmaceuticals that are excreted by glomerular filtration. Simplified methods have been proposed that require only one or two plasma samples in lieu of a more complete clearance curve. We examined the error introduced by this simplification. Forty patients were studied using a dual-isotope technique employing [99mTc]DTPA and [169Yb]DTPA, obtaining eight plasma samples for each clearance curve at intervals from 10 to 240 min after injection. Data were fit to several empirical or semiempirical formulae and also to a two-compartment computer model that permitted GFR estimation from only one or two data points. The computer model gave good fit, but so did several simpler methods. The error that results from replacing the complete clearance curve by a single 3-hr sample was about 8 ml/min (residual s.d.). By using two samples (at 1 and 3 hr), the error could be reduced to 4 ml/min. Recommended one- and two-sample methods are presented.  (+info)

Influence of dietary alfalfa:orchardgrass hay and lasalocid on in vitro estimates of dry matter digestibility and volatile fatty acid concentrations of cecal contents and rate of digesta passage in sows. (71/89)

Four mature crossbred sows were fistulated in the cecum, with two sows fed a corn-alfalfa:orchardgrass hay (46%) diet (CH) and two fed a corn-soybean meal diet (CS). Four experiments were conducted to evaluate buffers, incubation times, buffer pH and substrate and inocula sources in an in vitro, anaerobic, mixed-culture system. In vitro dry matter digestibility (IVDMD) and substrate solubility in buffer (SS) were determined. In Exp. 1, substrates were CH and CS diets with cecal inocula obtained from CH- and CS-fed sows. The bicarbonate (B) buffer resulted in lower (P less than .01) and less variable SS for all treatments. In vitro dry matter digestibility was higher (P less than .01) for the CS diet at both 24 and 48 h incubation. Use of the B buffer also resulted in higher (P less than .001) IVDMD values. In Exp. 2, substrates were either as in Exp. 1 or were freeze-dried cecal contents (CC) from CH- or CS-fed sows. In vitro dry matter digestibility of CC was lower (P less than .006) than IVDMD of diet, while IVDMD was higher (P less than .02) with cecal inocula than fecal inocula. In Exp. 3, substrate-inocula treatments were CH-CH, CH-CS, CS-CH and CS-CS. Substrate solubility was lower (P less than .05) at pH 5.8 than at pH 6.8. In vitro dry matter digestibility was higher when substrate and inocula were from the same source and at pH 5.8. In Exp. 4, CC and inocula were from sows fed CH and CS diets with or without lasalocid. In vitro dry matter digestibility was higher with CC from lasalocid-fed sows and inocula from sows fed no lasalocid. The CH diet resulted in higher acetate (Ac) and lower propionate (Pr) molar proportions than did the CS diet, while lasalocid increased molar proportion Pr and decreased molar proportion Ac in cecal contents from sows fed either diet. Corn-alfalfa:orchardgrass hay-fed sows had a faster rate of digesta passage and shorter cecal retention time than did CS-fed sows.  (+info)

Lanthanide markers in a single sample for nutrient studies in humans. (72/89)

Multiple Lanthanide markers were used to develop procedures for determinations of intake and apparent utilization of four nutrients using data from fecal analysis and known concentrations of markers in nutrients. Terbium oxide was given as the intake marker. All foods contained the other non-absorbed markers, each marker in direct proportion to the amount of a specific nutrient in each food. Nutrient markers were oxides of samarium, scandium, ytterbium, and europium. Fecal collection and subsequent analysis of nutrients and markers were completed. Fecal marker concentration stabilized 2 days following initiation of the marker regime. Thus, after 3 days, a single grab sample could be utilized to analyze for nutrient utilization. The ratio of nutrient marker proportional to nutrient and intake to nutrient excretion provides the data for the calculation of apparent utilization for as many nutrients as nutrient markers incorporated into the food. When direct and marker methods of determining nutrient intake and apparent utilization were compared, no significant differences were found for gross energy, fat, protein, and calcium.  (+info)