Trivedi S M, Humphrey R L, Braine H G, Frondoza C G
Transfusion. 1984 May-Jun;24(3):260-3. doi: 10.1046/j.1537-2995.1984.24384225035.x.
Hydroxyethyl starch (HES), a glucopyranose polymer used to enhance the yield of granulocytes during leukapheresis, was detected by periodic acid-Schiff (PAS) staining of 1-microliter samples following electrophoresis on thin agarose film. HES migrated with restricted electrophoretic mobility in the far gamma region, and the intensity of staining was found to be concentration dependent. Densitometer scanning showed a linear curve from 30 mg to 600 mg per dl, although bands were identified at concentrations lower than 30 mg per dl. Sera from 46 leukapheresis subjects showed the same restricted bands. HES measured retrospectively in sera obtained on days 1 to 400 following apheresis ranged from 675 to 30 mg per dl. The clearance of HES from the sera of four donors measured serially appeared biphasic with the first T1/2 of 0.4 to 6.4 days and the second T1/2 of 58 to 240 days. HES also was detectable in urine concentrated 100fold for as long as 7 days following leukapheresis . This simplified, and sensitive PAS glycoprotein staining method can be used to detect and follow HES concentrations in serum and may provide a new tool for the study of HES in leukapheresis donors.
羟乙基淀粉(HES)是一种用于在白细胞单采过程中提高粒细胞产量的吡喃葡萄糖聚合物,通过在薄琼脂糖膜上进行电泳后对1微升样品进行过碘酸希夫(PAS)染色来检测。HES在远γ区以受限的电泳迁移率迁移,并且发现染色强度与浓度有关。密度计扫描显示从每分升30毫克到600毫克呈线性曲线,尽管在低于每分升30毫克的浓度下也能识别出条带。46名白细胞单采受试者的血清显示出相同的受限条带。对白细胞单采后第1天至400天获得的血清进行回顾性测量,HES的含量范围为每分升675毫克至30毫克。对四名供体的血清中HES的清除情况进行连续测量,结果显示为双相清除,第一个半衰期为0.4至6.4天,第二个半衰期为58至240天。在白细胞单采后长达7天的时间里,在浓缩100倍的尿液中也能检测到HES。这种简化且灵敏的PAS糖蛋白染色方法可用于检测和追踪血清中的HES浓度,并可能为研究白细胞单采供体中的HES提供一种新工具。