In vitro closed loop optical network electrophysiology: An introduction

2013 ◽  
Author(s):  
A. El Hady ◽  
W. Stühmer
Keyword(s):  
Author(s):  
Christoph E. Schwarz ◽  
Gordon Lightbody ◽  
Ingo Müller-Hansen ◽  
Jörg Arand ◽  
Christian F. Poets ◽  
...  

BackgroundAdjusting the fraction of inspired oxygen (FiO2) delivered to preterm infants to keep their oxygen saturation within target range remains challenging. Closed-loop automated FiO2 control increases the time infants spend within the assigned target range. The delay with which FiO2 adjustments at the ventilator result in a change in the inspired gas limits the performance of both manual and automated controls.ObjectiveTo evaluate the equilibration time (Teq) between FiO2 adjustments and changes in FiO2 reaching the patient.MethodsIn vitro determination of the delay in FiO2 adjustments at the ventilator at 5 and 8 L/min of gas flow and two different humidifier/ventilator circuit volumes (840 and 432 mL).ResultsTeq values were 31, 23, 20 and 17 s for the volume–flow combinations 840 mL+5 L/min, 840 mL+8 L/min, 432 mL+5 L/min and 432 mL+8 L/min, respectively.ConclusionThe identified delay seems clinically relevant and should be taken into account during manual and automatic control of FiO2.


2019 ◽  
Vol 6 (2) ◽  
pp. 30 ◽  
Author(s):  
Chiara Campiglio ◽  
Francesca Ceriani ◽  
Lorenza Draghi

To fully exploit the potential of hydrogel micro-fibers in the design of regenerative medicinal materials, we designed a simple, easy to replicate system for cell embedding in degradable fibrous scaffolds, and validated its effectiveness using alginate-based materials. For scaffold fabrication, cells are suspended in a hydrogel-precursor and injected in a closed-loop circuit, where a pump circulates the ionic cross-linking solution. The flow of the cross-linking solution stretches and solidifies a continuous micro-scaled, cell-loaded hydrogel fiber that whips, bends, and spontaneously assembles in a self-standing, spaghetti-like patch. After investigation and tuning of process- and solution-related parameters, homogeneous microfibers with controlled diameters and consistent scaffolds were obtained from different alginate concentrations and blends with biologically favorable macromolecules (i.e., gelatin or hyaluronic acid). Despite its simplicity, this coaxial-flow encapsulation system allows for the rapid and effortless fabrication of thick, well-defined scaffolds, with viable cells being homogeneously distributed within the fibers. The reduced fiber diameter and the inherent macro-porous structure that is created from the random winding of fibers can sustain mass transport, and support encapsulated cell survival. As different materials and formulations can be processed to easily create homogeneously cell-populated structures, this system appears as a valuable platform, not only for regenerative medicine, but also, more in general, for 3D cell culturing in vitro.


2014 ◽  
Vol 15 (1) ◽  
Author(s):  
Soo Min Jang ◽  
Katie E Cardone ◽  
Thomas D Nolin ◽  
Darius L Mason ◽  
Darren W Grabe
Keyword(s):  

1998 ◽  
Vol 79 (01) ◽  
pp. 144-149 ◽  
Author(s):  
H. Feitsma ◽  
C. Kluft ◽  
J. L. M. Heeremans ◽  
R. Prevost ◽  
D. J. A. Crommelin

SummaryIn this study, the clot accumulation properties of liposome-coupled plasminogen were compared to those of free (non-liposomal) plasminogen in an in vitro, closed-loop, flow-system. After introduction of a clot into the closed system, double-radiolabelled plasminogen-liposomes were administered and the accumulation of radiolabel on the entire clot was measured.Liposomal plasminogen showed improved accumulation over free plasminogen, on both a fibrin clot and a whole blood clot. Moreover, once liposomal plasminogen was fibrin associated, it could not be washed away with buffer, in contrast to free plasminogen. Liposomal plasminogen was able to compete successfully with an excess of free plasminogen. The plateau levels for the accumulated amount of plasminogen depended on the incubated amount of plasminogen and were influenced by partial degradation of the clot. Furthermore, it was shown that a threshold liposomal plasminogen surface-density was needed for optimum clot accumulation.


2014 ◽  
Vol 136 (12) ◽  
Author(s):  
Joshua William Giles ◽  
Louis Miguel Ferreira ◽  
George Singh Athwal ◽  
James Andrew Johnson

In vitro active shoulder motion simulation can provide improved understanding of shoulder biomechanics; however, accurate simulators using advanced control theory have not been developed. Therefore, our objective was to develop and evaluate a simulator which uses real-time kinematic feedback and closed loop proportional integral differential (PID) control to produce motion. The simulator’s ability to investigate a clinically relevant variable—namely muscle loading changes resulting from reverse total shoulder arthroplasty (RTSA)—was evaluated and compared to previous findings to further demonstrate its efficacy. Motion control of cadaveric shoulders was achieved by applying continuously variable forces to seven muscle groups. Muscle forces controlling each of the three glenohumeral rotational degrees of freedom (DOF) were modulated using three independent PID controllers running in parallel, each using measured Euler angles as their process variable. Each PID controller was configured and tuned to control the loading of a set of muscles which, from previous in vivo investigations, were found to be primarily responsible for movement in the PID’s DOF. The simulator’s ability to follow setpoint profiles for abduction, axial rotation, and horizontal extension was assessed using root mean squared error (RMSE) and average standard deviation (ASD) for multiple levels of arm mass replacement. A specimen was then implanted with an RTSA, and the effect of joint lateralization (0, 5, 10 mm) on the total deltoid force required to produce motion was assessed. Maximum profiling error was <2.1 deg for abduction and 2.2 deg for horizontal extension with RMSE of <1 deg. The nonprofiled DOF were maintained to within 5.0 deg with RMSE <1.0 deg. Repeatability was high, with ASDs of <0.31 deg. RMSE and ASD were similar for all levels of arm mass replacement (0.73–1.04 and 0.14–0.22 deg). Lateralizing the joint’s center of rotation (CoR) increased total deltoid force by up to 8.5% body weight with the maximum early in abduction. This simulator, which is the first to use closed loop control, accurately controls the shoulder’s three rotational DOF with high repeatability, and produces results that are in agreement with previous investigations. This simulator’s improved performance, in comparison to others, increases the statistical power of its findings and thus its ability to provide new biomechanical insights.


1913 ◽  
Vol 17 (3) ◽  
pp. 307-324
Author(s):  
G. H. Whiffle ◽  
H. B. Stone ◽  
B. M. Bernheim

The blood of closed duodenal loop dogs is not toxic to normal dogs. The blood of dogs that have been fatally poisoned with duodenal loop fluid is likewise non-toxic to normal dogs. The mucosa of closed or drained duodenal loops contains a toxic substance quite similar to the toxic material found in the lumen of the closed loops. This toxic substance is absorbed from the mucosa itself and not from the lumen of the drained loops. The same is probably true of the closed loops which have an intact mucosa. It seems highly probable that the poison is formed by the mucosa and is in great part absorbed directly from it by the blood. Normal intestinal mucosa contains no toxic substance nor can it neutralize in vitro the toxic substance produced in the closed loops. There is no evidence that the toxic material when given intravenously is excreted by the intestine or held by the intestinal mucosa in any demonstrable form. The toxic substance is not absorbed from the normal intestinal tract. Destruction of the mucosa in a closed loop by means of sodium fluoride prevents the formation of the toxic substance. This fact furnishes the final proof that the mucosa is the essential factor in the elaboration of the poisonous material.


Cytometry ◽  
1987 ◽  
Vol 8 (1) ◽  
pp. 101-103 ◽  
Author(s):  
W. H. Schuette ◽  
C. Burch ◽  
P. O. Roach ◽  
J. E. Parrillo

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