Abstract
The transport of deferiprone (L1) in normal (N), sickle (S) and thalassaemic (T) red blood cells (RBC) was determined by incubation with 14C-L1 at 37°C. Following incubation with 0.5 mM 14C-L1 for 4h, the intracellular concentration of L1 in T RBC was 3 times higher than was found extracellularly. In contrast, no concentration gradient across N and S RBC membranes was detected. Efflux studies showed that T RBC released only 17 ± 2% of 14C-L1 into the extracellular space. We hypothesize that L1 accumulation in T RBC results from their high content of chelatable iron and formation of large, hydrophilic L1-Fe(III) complexes trapped within the cytosol.
Original language | English |
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Pages (from-to) | 1081-1083 |
Number of pages | 3 |
Journal | British Journal of Haematology |
Volume | 105 |
Issue number | 4 |
DOIs | |
Publication status | Published - 1999 |
Keywords
- Deferiprone
- Erythrocytes
- Sickle cell disease
- Thalassaemia
- Transport