Kinoshita Y, Ohta K, Yamane T, Hino M, Takubo T, Samori T, Tatsumi N
Department of Clinical and Laboratory Medicine, Osaka City University Medical School, Asahimachi, Osaka, Japan.
J Clin Lab Anal. 2000;14(4):180-7. doi: 10.1002/1098-2825(2000)14:4<180::aid-jcla7>3.0.co;2-e.
To evaluate the feasibility of a synthetic polymer, sulphonated polyisoprene (SPIP), to be used as a new laboratory anticoagulant, hematological items were compared between blood samples anticoagulated with EDTA and SPIP, as were biochemical and electrolyte items between serum samples and SPIP-anticoagulated blood. Among hematological items, the average platelet count of the SPIP group was significantly lower than that of the EDTA group, due to platelet aggregation in the SPIP group. Addition of kanamycin to SPIP, but not of aspirin or prostaglandin E1, restored platelet count to about 80% of that in the EDTA group, and increased coefficients of correlation with the EDTA group for most hematological items examined. For biochemical and electrolyte items, high (> 0.95) correlation coefficients were obtained for 15 of 18 items between the serum and SPIP-anticoagulated samples. However, for some of these items, the addition of kanamycin decreased coefficients of correlation. Thus, SPIPs are excellent candidates for new anticoagulants that can be used for evaluation of hematological, biochemical, and electrolyte items with a single test tube in routine laboratory work. However, some improvements are required for use of kanamycin as an additive to inhibit platelet aggregation induced by SPIP, and in maintaining reliability of biochemical and electrolyte measurements.
为评估合成聚合物磺化聚异戊二烯(SPIP)作为新型实验室抗凝剂的可行性,对用乙二胺四乙酸(EDTA)和SPIP抗凝的血样的血液学指标进行了比较,同时也对血清样本与SPIP抗凝血液的生化和电解质指标进行了比较。在血液学指标中,由于SPIP组中血小板聚集,SPIP组的平均血小板计数显著低于EDTA组。向SPIP中添加卡那霉素可使血小板计数恢复至EDTA组的约80%,而添加阿司匹林或前列腺素E1则无此效果,并且添加卡那霉素后,大多数检测的血液学指标与EDTA组的相关系数增加。对于生化和电解质指标,血清样本与SPIP抗凝样本之间18项指标中的15项获得了高(>0.95)相关系数。然而,对于其中一些指标,添加卡那霉素会降低相关系数。因此,在常规实验室工作中,SPIP是可用于在单个试管中评估血液学、生化和电解质指标的新型抗凝剂的极佳候选物。然而,使用卡那霉素作为添加剂来抑制SPIP诱导的血小板聚集以及维持生化和电解质测量的可靠性仍需要一些改进。