In vitro and in situ nutrient degradability of barley and wheat milling byproducts

1998 ◽  
Vol 78 (3) ◽  
pp. 457-459 ◽  
Author(s):  
A. F. Mustafa ◽  
J. J. McKinnon ◽  
D. A. Christensen

A study was conducted to estimate nutrient degradability of barley milling byproducts (BMBP) using in vitro and in situ techniques. Three levels of milling (5.9, 9.5 and 17%), representing the proportion of byproduct to the original grain weight were tested. A wheat byproduct (WMBP), milled at 5.9% was used for comparison. Results indicated that 5.9% WMBP was more degradable than the BMBP. Within the BMBP, the 17% BMBP was more degradable than the 5.9 and the 9.5% BMBP. No differences in nutrient degradability were observed between the 5.9 and the 9.5% BMBP. Key words: Barley, wheat, milling byproducts, nutrient degradability

1996 ◽  
Vol 76 (4) ◽  
pp. 625-628 ◽  
Author(s):  
A. F. Mustafa ◽  
D. A. Christensen ◽  
J. J. McKinnon

The in vitro and in situ nutrient degradabilities of fenugreek hay and straw relative to late-cut alfalfa hay and barley straw were determined. Results indicated that the nutritive value of fenugreek hay was comparable to late cut alfalfa hay while that of genugreek straw was lower than barley straw. Key words: Fenugreek, hay, straw


1995 ◽  
Vol 75 (3) ◽  
pp. 485-487 ◽  
Author(s):  
K. B. Lehman ◽  
E. K. Okine ◽  
G. W. Mathison ◽  
J. Helm

Differences in in situ dry matter degradabilities occurred at all incubation times when 22 cultivars of barley gram grown at three locations were examined. Rapidly and slowly degradable fractions ranged from 25 to 40% and from 49 to 65%, respectively. Rates of degradation ranged from 23 to 35% h−1 (P = 0.03). Key words: Barley, cultivars, in situ, degradability, location


Phlebologie ◽  
2007 ◽  
Vol 36 (05) ◽  
pp. 237-244 ◽  
Author(s):  
B. Lun ◽  
J. F. Uhl ◽  
Y. Bringer ◽  
W. Blättler

Summary Objective: The force exerted on a limb by a medical compression stocking (MCS) is given by the properties of the yarn and the technique of knitting. The pressure determined by the manufacturer should be the one acting on the leg provided the stocking fits the leg shape. However, the interface pressure is governed by additional factors which act simultaneously in a poorly defined manner. We sorted out the different material- and patient-related components and assessed their relative role combining in vitro with in situ techniques. Design and method: The force exerted by the stockings was measured with the Zwick and Hosy dynamometers and the pressure exerted on the leg with the SIGaT instrument placed underneath the stockings at various sites. Leg circumference was determined with the Perometer and local radius calculated from computer tomographic slices and assessed with templates. Stockings exerting ankle pressures between 10 and 40 mmHg were tested. Subjects serving in the various experiments were selected from a pool of 28 healthy volunteers. Results: All stockings exerted the predefined pressure when measured at the stocking/leg-interface (in situ) and on the dynamometer (in vitro) provided the local leg curvature was taken into account. The stockings showed slightly different elastic properties (pressure amplitude difference upon leg movement 2–6mmHg). The interface pressure varied significantly when measured at different angular positions on the same circumference (range of change +40%; –20%). The differences were strongly correlated with the local radius (range of variation along the calf circumference 35–125 mm). The differences of local radii got smaller with higher interface pressures. Leg movements provoked simultaneous increases and decreases of interface pressure of up to 15 mmHg depending on the site of measurement. Leg circumference varied only slightly with movements pointing in either direction: 0.25 cm at the ankle (range +0.4; –0.4) and 0.33 cm at the calf (range +1.05; –1.45), respectively. The compressibility of the underlying tissue had no effect on the interface pressure. Conclusions: The interface pressure can be assessed reliably in vitro and in situ. It shows complex, quantitatively important non-uniform local variations both when measured along a given leg circumference at rest and when monitored at one particular site during movements. The changes reflect the discontinuity of the leg configuration and further alterations of the silhouette occurring with every muscle activation. Clearly, a massage effect of stockings is documented which does not necessarily reflect a global effect exerted on the leg.


2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
A. Falsafi ◽  
J. D. Oxman ◽  
P.-H. Tse ◽  
T. T. Ton

Aim. This paper presents a simple, versatile in vitro methodology that enables indirect quantification of shrinkage and expansion stresses under clinically relevant conditions without the need for a dedicated instrument.Methods. For shrinkage effects, resulting cusp deformation of aluminum blocks with MOD type cavity, filled with novel filling compositions and commercial cements, has been measured using a bench-top micrometer and a Linear Variable Differential Transformer (LVDT, a displacement transducer) based instrument.Results. The results demonstrated the validity of the proposed simple methodology. The technique was successfully used in longer-term measurements of shrinkage and expansion stress for several dental compositions.Conclusions. In contrast to in situ techniques where a measuring instrument is dedicated to the sample and its data collection, the proposed simple methodology allows for transfer of the samples to the environment of choice for storage and conditioning. The presented technique can be reliably used to quantify stress development of curing materials under clinically relevant (oral) conditions. This enables direct examination and comparison of structural properties corresponding to the final stage of formed networks. The proposed methodology is directly applicable to the study of self-curing systems as they require mouth-type conditions (temperature and humidity) to achieve their designed kinetics and reactions.


2019 ◽  
Vol 4 (1) ◽  
pp. 141-148 ◽  
Author(s):  
Mary E DeFeo ◽  
Kelsey V Shampoe ◽  
Pedro H V Carvalho ◽  
Flavia A S Silva ◽  
Tara L Felix

Abstract Objectives were to compare in vitro and in situ disappearance of dry matter (DM), neutral detergent fiber (NDF), and starch of traditional (unprocessed and rolled) and hulless (unprocessed) barley. Experiment 1: three barley sources were compared using in vitro techniques. The sources were: 1) traditional barley that was not processed, 2) traditional barley processed through a roller mill, and 3) hulless barley that was not processed. For in vitro incubation, each barley source was ground through a 1-mm screen. Ground barley sources were weighed into bags (25 micron porosity) and incubated in ruminal fluid from two steers fed 80% rolled corn for 3, 6, 12, 24, 48, or 72 h. Intact bags were assayed for NDF; remaining bags were opened and the residual was removed and analyzed to determine disappearance of DM and starch. Experiment 2: the barley sources used in Exp. 1 were compared using in situ techniques. For in situ analysis, each barley source was ground in a Wiley mill with no screen to mimic mastication. Artificially masticated samples were weighed into Dacron bags (50 ± 10 micron porosity) and incubated in eight ruminally fistulated steers (n = 8) for 3, 6, 12, 24, 48, and 72 h. Residual contents were analyzed to determine in situ disappearance of DM, NDF, and starch. Data were analyzed using the MIXED procedures of SAS (9.4 SAS Institute, Cary, NC) with repeated measures. DM disappearance was greatest (P < 0.05) for hulless barley in vitro and for rolled barley in situ, regardless of time postincubation. For both trials, NDF disappearance was greatest (P < 0.05) for hulless barley, regardless of time postincubation. Starch disappearance at all time points was greatest (P < 0.05) for rolled barley in situ. Starch disappearance was greater (P < 0.05) for hulless barley at 6 h of in vitro incubation compared to rolled and unprocessed barley, whereas starch disappearance in vitro was comparable (P = 0.60) between barley sources. When the grains were compared in vitro, minor differences were noted, presumably because barley sources were finely ground prior to incubation. Compared to in vitro estimates, in situ techniques had greater variation in ruminal degradation estimates. Differences observed between in situ and in vitro techniques are driven largely by differences between the procedures. Although laboratory methods are widely used to estimate ruminal degradation, these techniques did not provide comparable estimates of ruminal degradation of barley.


Pharmaceutics ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 898
Author(s):  
Isabela Fanelli Barreto Biscaia ◽  
Samantha Nascimento Gomes ◽  
Larissa Sakis Bernardi ◽  
Paulo Renato Oliveira

Cocrystals have gained attention in the pharmaceutical industry due to their ability to improve solubility, stability, in vitro dissolution rate, and bioavailability of poorly soluble drugs. Conceptually, cocrystals are multicomponent solids that contain two or more neutral molecules in stoichiometric amounts within the same crystal lattice. There are several techniques for obtaining cocrystals described in the literature; however, the focus of this article is the Reaction Crystallization Method (RCM). This method is based on the generation of a supersaturated solution with respect to the cocrystal, while this same solution is saturated or unsaturated with respect to the components of the cocrystal individually. The advantages of the RCM compared with other cocrystallization techniques include the ability to form cocrystals without crystallization of individual components, applicability to the development of in situ techniques for the screening of high quality cocrystals, possibility of large-scale production, and lower cost in both time and materials. An increasing number of scientific studies have demonstrated the use of RCM to synthesize cocrystals, mainly for drugs belonging to class II of the Biopharmaceutics Classification System. The promising results obtained by RCM have demonstrated the applicability of the method for obtaining pharmaceutical cocrystals that improve the biopharmaceutical characteristics of drugs.


1991 ◽  
Vol 71 (3) ◽  
pp. 739-754 ◽  
Author(s):  
E. M. Kendall ◽  
J. R. Ingalls ◽  
R. J. Boila

The rumen degradability and postruminal digestion of rumen escape dry matter (DM), nitrogen (N) and metabolically essential amino acids (EAA) for canola meal (CM) from five different processing plants (samples 1–5) and one sample of soybean meal (SBM) were compared. Rumen degradability was estimated by incubating sample-filled small nylon bags in situ in the rumen of steers for 0, 4, 8, 12, 16 and 30 h. Postruminal digestion was estimated using a sequence of ruminal in situ incubations for 0, 4, 8, 12 and 16 h, in vitro incubation in an acid-pepsin solution and a mobile nylon bag technique distal to the abomasum. The rumen escape of nutrients for CM1 was consistently lower compared to other CM samples, while CM4 resulted in the highest escape of nutrients at 30 h. An estimate of maximum degradability of EAA measured at 30 h differed among CM samples, with the rumen escape of EAA being CM4 > CM2 = CM5 ≥ CM1 = CM3 > SBM. The DM, N and EAA content of mobile bag residues was relatively uniform among CM samples, particularly after 12 and 16 h of ruminal fermentation, but was higher for CM than for SBM, probably due to a low digestibility of CM hulls. The rumen degradability of CM from different processing plants differed and as a consequence the postruminal digestion of nutrients in CM differed. Key words: Canola meal, rumen degradability, postruminal digestion, dry matter, nitrogen, amino acids


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