K Nakai, H Abe, N Matsuda, M Kobayashi, H Ikeda, S Sekiguchi, E Tsuchida
{"title":"Development of analytical methods to evaluate SFH.","authors":"K Nakai, H Abe, N Matsuda, M Kobayashi, H Ikeda, S Sekiguchi, E Tsuchida","doi":"10.3109/10731199209119667","DOIUrl":null,"url":null,"abstract":"<p><p>For the determination of stroma content in SFH, two analytical methods were developed, the HPLC-UV for phospholipids and the enzyme immunoassay for blood group antigen. These analytical methods were applied to evaluate three representative SFH preparations. The 36,000 x g centrifugation method was shown to contain higher amount of stroma components. On the other hand, the BMM-40 nm and the ultrafiltration method with a 100 kd membrane was shown to remove more than 99.7% of phospholipids and almost all of blood group antigen from hemoglobin solutions. These results demonstrated that these analytical methods were very useful in evaluating any highly purified hemoglobin solutions.</p>","PeriodicalId":77039,"journal":{"name":"Biomaterials, artificial cells, and immobilization biotechnology : official journal of the International Society for Artificial Cells and Immobilization Biotechnology","volume":"20 2-4","pages":"447-51"},"PeriodicalIF":0.0000,"publicationDate":"1992-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/10731199209119667","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomaterials, artificial cells, and immobilization biotechnology : official journal of the International Society for Artificial Cells and Immobilization Biotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/10731199209119667","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
For the determination of stroma content in SFH, two analytical methods were developed, the HPLC-UV for phospholipids and the enzyme immunoassay for blood group antigen. These analytical methods were applied to evaluate three representative SFH preparations. The 36,000 x g centrifugation method was shown to contain higher amount of stroma components. On the other hand, the BMM-40 nm and the ultrafiltration method with a 100 kd membrane was shown to remove more than 99.7% of phospholipids and almost all of blood group antigen from hemoglobin solutions. These results demonstrated that these analytical methods were very useful in evaluating any highly purified hemoglobin solutions.
建立了两种测定SFH基质含量的方法:高效液相色谱-紫外分光光度法(HPLC-UV)测定磷脂和酶免疫分析法(elisa)测定血型抗原。这些分析方法用于评价三种具有代表性的SFH制剂。36,000 x g离心方法被证明含有更多的基质成分。另一方面,BMM-40 nm和100 kd膜的超滤方法可以从血红蛋白溶液中去除99.7%以上的磷脂和几乎所有的血型抗原。这些结果表明,这些分析方法是非常有用的评价任何高纯度的血红蛋白溶液。