PubMed · 15402701
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B K JENSEN, K A JENSEN. 1950-01-07. A steric cabinet for producing injectabilia.. https://pubmed.ncbi.nlm.nih.gov/15402701/
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Nowadays drug stores of military-and-field medical organizations use the method of distillation for obtaining cleaned water and water for injection and use distillators as a technical means, which does not ensure that the water obtained has stated indices of quality. It was found out that it is the most efficient to use the technology basing on the complex usage of filtering, osmotic, ionic processes for obtaining cleaned water and water for injection from surface natural springs, which ensures minimal usage of resources and energy and the unity of constructional and technological peculiarities of cleaning water methods.
PURPOSE: To assess the accuracy and precision of methods in clinical use for intraocular drug injection. DESIGN: Experimental laboratory investigation. METHODS: A total of 800 injections were performed using 20 different 1-ml syringes at intended volumes of 0.10 ml and 0.05 ml. The volume of each injection was calculated from mass of water delivered onto an analytic balance. RESULTS: The mean measured volume delivered was less than the intended volume for every syringe (P <.001 for each syringe at each volume). A total of 7% and 22% of injections differed by 20% or more from the intended volumes of 0.10 ml and 0.05 ml, respectively. Overdelivery of volume was uncommon. CONCLUSION: Clinically relevant materials and methods used for intraocular injection of drugs systematically underdelivered the intended volume.
AIM: To determine vitamin B1 in pharmaceutical preparations by chemiluminescence (CL) flow sensor. METHODS: When 200 microL of Na3PO4 was passed through an anion exchange column, K3Fe(CN)6 was eluted from the resin and then mixed with the vitamin B1 stream containing NaOH to product CL, by the fast oxidation reaction between vitamin B1 and K3Fe(CN)6 in alkaline solution. RESULTS: The CL emission intensity was correlated with the vitamin B1 concentration in the range 1.0 x 10(-5) to 1.0 x 10(-3) mol.L-1 and the detection limit was 8.0 x 10(-6) mol.L-1 (3 sigma). A complete analysis, including sampling and washing, can be performed within 2 min with a relative standard deviation of less than 4.0%. CONCLUSION: The vitamin B1 flow sensor was stable for over 200 analyses and has been applied successfully to determination of vitamin B1 in pharmaceutical preparations.