1985
DOI: 10.1046/j.1537-2995.1985.25485273810.x
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Preparation of blood components with saline‐adenine‐glucose‐phosphate‐ maltose quadruple‐pack system

Abstract: A saline-adenine-glucose-phosphate-maltose (SAGP-maltose) quadruple-pack system was devised to improve the conventional method of preparing blood components. One of the features of this method is that high-speed centrifugation was used as the initial spin in the two-step centrifugation of whole blood. This feature permitted the removal of the buffy coat from red cells at the same time the platelets were isolated. Since the platelets were concentrated without forming a button, the damage to the platelets due to… Show more

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Cited by 15 publications
(7 citation statements)
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“…Platelets were counted electronically (Coulter Thrombocounter), hypotonic shock response determined as described by Tandy and Taylor [25]. Electron microscopy of platelets was performed according to Archer et al [26], and red cell morphology assessed by light microscopy as described by Uda et al [27], based on cell forms defined by Bessis [28]. Sterility testing was performed in a manner similar to that suggested by Puckett [29].…”
Section: Processing Of Bloodmentioning
confidence: 99%
“…Platelets were counted electronically (Coulter Thrombocounter), hypotonic shock response determined as described by Tandy and Taylor [25]. Electron microscopy of platelets was performed according to Archer et al [26], and red cell morphology assessed by light microscopy as described by Uda et al [27], based on cell forms defined by Bessis [28]. Sterility testing was performed in a manner similar to that suggested by Puckett [29].…”
Section: Processing Of Bloodmentioning
confidence: 99%
“…Citrate was assayed colorimetrically [24], Platelets were counted electronically (Coulter Thrombocounter), hypotonic shock response determined as described by Tandy and Taylor [25]. Electron microscopy of platelets was per formed according to Archer et al [26], and red cell morphology assessed by light microscopy as described by Uda et al [27], based on cell forms defined by Bessis [28]. Sterility testing was performed in a manner similar to that suggested by Puckett [29].…”
Section: Processing Of Bloodmentioning
confidence: 99%
“…Preparation and preseroation of red blood cells with u sextuple-hag system Figure 1 shows the sextuple-bag system (Kawasumi Kagakukogyo Co., Ltd, Tokyo, Japan) according to our specifications: the primary bag contains 56 ml of citrate-phosphate-glucose (CPD) solution, and the third to fifth bags contain 140 ml of SAGP-maltose solution (Uda et al, 1985) composed of 2 mM adenine, 50 mM glucose, 20 mM disodium hydrogen phosphate, 60 mM maltose, and approximately 80 mM sodium chloride, with an osmotic pressure of approximately 300 mOsm. The SAGP-maltose solution was sterilized separately by filtration through a 0.22-pm membrane filter (Japan Milipore Co., Ltd, GSWP 04700, Tokyo, 257 Japan), and then added to the third to fifth satellite bags of the previously autoclaved sextuple-bag system.…”
Section: Materials a N D Methodsmentioning
confidence: 99%
“…ATP, ADP and AMP were measured spectrophotometrically according to an enzymatic method (Jaworek et a[., 1974). A morphology score was determined as described previously (Uda et al, 1985;Ohkuma & Uda, 1986). Briefly, a morphology score was calculated from the percentage of red cells of each of four morphological types, according to the modification of the classification of Bessis (Brecher & Bessis, 1972), and given an integral value from 3 to 0 (discocyte = 3, echinocyte I = 2, echinocyte I1 = 1, spherocyte = 0).…”
Section: In-uitro Tests For Stored Red Blood Cellsmentioning
confidence: 99%
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