dc.creatorConesa, Angela
dc.creatorPérez, Carlos
dc.creatorRivera, Henry
dc.creatorAldrey, Oscar
dc.creatorBianco Colmenares, Nicolás E.
dc.creatorDe Sanctis, Juan B.
dc.date2017-03-02T14:46:06Z
dc.date2017-03-02T14:46:06Z
dc.date1997
dc.date.accessioned2022-10-28T01:21:53Z
dc.date.available2022-10-28T01:21:53Z
dc.identifier0269-8951
dc.identifierhttp://hdl.handle.net/10872/14717
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4948333
dc.descriptionA new method for normodense eosinophil purification is proposed. It is based on the use of high-density Ficoll-Hypaque (density = 1.114 g mL-1) instead of dextran sedimentation plus standard Ficoll-Hypaque, before discontinuous Percoll gradient centrifugation. Eosinophils from 11 controls and 11 eosinophilic patients were studied. The density distribution of eosinophils was similar in both groups. However, eosinophilic patients showed a significant increase in the absolute count of hypodense eosinophils. Normodense eosinophil purity and recovery were significantly higher in controls as compared with eosinophilic patients (p < 0.05). High-density Ficoll-Hypaque allowed separation of mononuclear and polymorphonuclear cells with high purity and recovery using a single centrifugation step. It also reduces one step in eosinophil purification as compared to the standard method. Thirdly, contrary to the single anti-CD16 magnetic bead separation method, it allows the isolation of normodense and hypodense eosinophils. In summary, this method is economic, reliable and permits the purification of different leucocyte populations.
dc.languageen
dc.publisherMedical science research
dc.relationVol. 25;No. 11 pp 751-755
dc.subjectnormodense eosinophil
dc.subjecthigh-density Ficoll-Hypaque
dc.subjecteosinophil purification
dc.subjectmononuclear
dc.subjectpolymorphonuclear cells
dc.subjectanti-CD16
dc.subjecthypodense eosinophils
dc.subjectleucocyte populations
dc.titleHigh-density Ficoll-Hypaque as an alternative method of eosinophil purification
dc.typeArticle


Este ítem pertenece a la siguiente institución