Literature DB >> 9352140

The use of automated HPLC to detect and quantitate haemoglobins.

B J Wild1, A D Stephens.   

Abstract

The introduction of automation for haemoglobinopathy screening is an important advance in technology for haematology laboratories. This paper evaluates the utility of an automated HPLC instrument, the Bio-Rad 'Variant' for the detection and quantitation of the normal haemoglobins (Hb A, A2 and F) and the common abnormal haemoglobins (Hb S, C, DPunjab, E, OArab and Lepore) which need to be evaluated in laboratories undertaking carrier and/or neonatal screening for sickle cell and thalassaemia. The instrument only uses a small amount of whole blood (5 microliters), a 3 mm disc from a Guthrie spot may also be used for analysis of samples from neonates. It uses a 100 place automatic sampler with a cycle time of 6.5 min for adult samples (using the 'Beta Thalassaemia Short' reagent pack) and 3 min for neonatal samples. The automatic sampler also allows samples to be analysed 'out of hours'. A 'STAT'; position allows urgent samples to be analysed before, or during, a routine analytical run. All reagents, other consumables and application notes are provided by the suppliers. Other types of reagent packs, such as the 'Sickle Cell Short' for neonatal screening were not assessed during this study.

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Year:  1997        PMID: 9352140

Source DB:  PubMed          Journal:  Clin Lab Haematol        ISSN: 0141-9854


  5 in total

1.  Hemoglobin Pakse: presence on red blood cell membrane and detection by polymerase chain reaction-single-strand conformational polymorphism.

Authors:  Chairat Turbpaiboon; Atchasai Siritantikorn; Wanna Thongnoppakhun; Duangkamon Bunditworapoom; Chanin Limwongse; Pa-thai Yenchitsomanus; Noppadol Siritanaratkul; Prapon Wilairat
Journal:  Int J Hematol       Date:  2004-08       Impact factor: 2.490

Review 2.  The pressing need for point-of-care diagnostics for sickle cell disease: A review of current and future technologies.

Authors:  Patrick T McGann; Carolyn Hoppe
Journal:  Blood Cells Mol Dis       Date:  2017-08-08       Impact factor: 3.039

3.  Molecular basis and hematological features of hemoglobin variants in Southern Thailand.

Authors:  Vannarat Saechan; Chawadee Nopparatana; Chamnong Nopparatana; Suthat Fucharoen
Journal:  Int J Hematol       Date:  2010-09-14       Impact factor: 2.490

4.  High performance liquid chromatography (HPLC) as a screening tool for classical Beta-thalassaemia trait in malaysia.

Authors:  E George; A R Jamal; F Khalid; K A Osman
Journal:  Malays J Med Sci       Date:  2001-07

5.  Detection of Abnormal Hemoglobin Variants by HPLC Method: Common Problems with Suggested Solutions.

Authors:  Leela Pant; Dipti Kalita; Sompal Singh; Madhur Kudesia; Sumanlata Mendiratta; Meenakshi Mittal; Alka Mathur
Journal:  Int Sch Res Notices       Date:  2014-10-12
  5 in total

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