About: Burette is a research topic. Over the lifetime, 511 publications have been published within this topic receiving 1884 citations. The topic is also known as: buret.
TL;DR: Change of in-line burettes in intensive care at 48-hour intervals is safe and should result in substantial cost savings and be associated with primary bacteremia.
Abstract: No studies of safety in changing intravenous systems containing in-line burettes at 48 hours in an intensive care setting have been performed. Patients entering a surgical intensive care unit were alternatively assigned to have any line with an in-line burette changed at either 24-hour (64 patients) or 48-hour (59 patients) intervals. Daily quantitative cultures with a 2-mL aliquot of burette fluid were obtained. Contaminated burette fluid was detected in nine of 452 (2.0%; 95% confidence interval, 0.7% to 3.3%) samples from 24-hour interval burettes and in nine of 224 (4.0%; 95% confidence interval, 1.4% to 6.6%) samples from 48-hour interval burettes. Bacterial contamination of burette fluid with ten or more colonies per milliliter occurred in only five (1.1%) cultures from patients in the 24-hour interval group compared with only two cultures (0.9%) in the 48-hour group. None of the contaminated burette fluids was associated with primary bacteremia. Change of in-line burettes in patients in intensive care at 48-hour intervals is safe and should result in substantial cost savings. ( JAMA 1984;251:2112-2115)
TL;DR: In this paper, a program was developed for the computer-controlled cooperation of four commercially available stepmotor-driven burettes to form density gradients in polyacrylamide gels and solute gradients for other purposes such as centrifugation and low pressure chromatography.
Abstract: A program has been developed for the computer-controlled cooperation of 4 commercially available stepmotor-driven burettes to form density gradients in polyacrylamide gels and solute gradients for other purposes such as centrifugation and low pressure chromatography. The slope of the gradients was defined by entering up to 200 endpoints of straight lines with the percentage of the total volume and the concentration of the gradient-forming solute as coordinates. The possible minimum increment of the discontinuous gradients is 0.5 % of the total range. They are mixed at variable flow rate by two burettes containing the high and low density acrylamide solutions and two additional burettes for the admixture of two catalysts at variable volume proportions. Within 10 min gradients with total volumes between 4 and 650 ml can be delivered. Gradient volumes smaller than 4 ml are possible if an average increment of > 0.5 % is accepted. The program meets the requirements of reproducibility for high resolution gradient gel electrophoresis and isoelectric focusing in immobilized pH gradients. All input data for the definition of the gradients can be displayed as a hard copy by a matrix printer and stored on tape. Thus the device meets the requirements of proper documentation of a given gradient in a publication and for reproduction in another laboratory. Other types of gradients for volumes of up to 1.4 liters can be produced by a subprogram converting the 4 burettes into a gradient pump with continuous outflow as used for column chromatography. The speed is variable between 0.4 ml and 5.2 liters per hour with minor pulsation only in the very low range.
TL;DR: In this paper, a burette chamber is provided which includes a primary and a secondary compartment, a wall member separating the primary and secondary compartments with the wall member providing an opening for communication between the secondary and primary compartments.
Abstract: A burette chamber is provided which includes a primary and a secondary compartment, a wall member separating the primary and secondary compartments with the wall member providing an opening for communication between the primary and secondary compartments. When the burette chamber is included in an intravenous solution administration set, the set can continuously administer IV solution to a patient as well as to allow intermittent administration of medicaments with return to the continuous administration of IV solution to the patient after completion of medicament administration.
TL;DR: In this paper, the performance of a new system for sequential injection analysis equipped with a liquid driver constituted by an ordinary burette for conventional automatic titrations actuated by a stepper motor was assessed.