35 results match your criteria: "Hospital Products Division[Affiliation]"

A factorial design study on the physical stability of 3-in-1 admixtures.

J Pharm Pharmacol

November 1993

Hospital Products Division, Abbott Laboratories, Abbott Park, IL 60064.

The effects of dextrose concentration, the compounding method, and storage conditions, on the physical stability of 3-in-1 admixtures were investigated using a 2n factorial design. The main effect of these three variables on the weight percent of oil globules larger than 5 microns (by HIAC) was found to be statistically significant. However, the effects of interaction amongst these variables, except the two-way interaction between dextrose concentration and storage conditions, were found to be statistically insignificant.

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Siliconized stoppers, when used with parenteral drug products, have been shown to be a source of particulate contamination. In this study, five different variables: pH of the solution, buffer concentration, Teflon coating on the stopper, autoclaving cycle (F0), and lot-to-lot variation of the siliconization process were evaluated using an eight-run Plackett-Burman design with respect to their impact on the level of particulate contamination from siliconized stoppers. Results show that pH of the solution can significantly affect the particulate level of samples using siliconized stoppers (p < 0.

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The sorption of calcitriol into PVC from an injectable formulation containing Tween 20, a nonionic surfactant, was studied. The amount of drug sorbed by the plastic decreased as the concentration of the surfactant increased. The apparent partition parameter of the drug between PVC strips and the solution was experimentally determined at three different concentrations of the surfactant.

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The stability of commercially formulated calcitriol 1 and 2 micrograms/mL and calcitriol formulation subsequently diluted to 0.5 microgram/mL in 0.9% sodium chloride injection, 5% dextrose injection, or water for injection was evaluated after eight hours' storage in polypropylene syringes.

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The stability of ganciclovir 1 and 5 mg/mL in 5% dextrose injection and in 0.9% sodium chloride injection was studied at 25 degrees C and 5 degrees C over 35 days. Ganciclovir (as the sodium salt) was added to 120 polyvinyl chloride bags containing either 5% dextrose injection or 0.

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Parliamentary procedure is the greatest ally a committee chair or presiding officer can have. It is also an ally for the knowledgeable committee member. The key procedures are the rules governing motions.

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The stability of total nutrient admixtures (TNAs) prepared from dextrose and amino acid injections commercially packaged in a dual-chamber container and a safflower-soybean oil fat emulsion was studied. The admixtures studied were divided into two groups. Group 1 admixtures represented 14 combinations of Aminosyn II, dextrose, and Liposyn II.

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The maximum solubilities of calcium and phosphate in neonatal total parenteral nutrient (TPN) solutions compounded using Aminosyn-PF or TrophAmine amino acid injection were determined. Eight solutions were compounded from Sterile Water for Injection, USP, 50% dextrose injection, usual electrolytes and trace metals, and Aminosyn-PF 7% or TrophAmine 6% to obtain concentrations of amino acids 2.5% and dextrose 25% and amino acids 1% and dextrose 10%.

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