Autofluorescence of condensed heme aggregates in malaria pigment and its synthetic equivalent hematin anhydride (beta-hematin)

The condensed crystalline phase of iron(III) protoporphyrin IX either isolated from parasite culture as malaria pigment (hemozoin) or synthetic equivalent hematin anhydride exhibits a solid-state autofluorescence characterized by an excitation maximum of 555 nm and an emission maximum of 577 nm. The...

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Vydáno v:The journal of physical chemistry. B Ročník 113; číslo 24; s. 8391 - 8401
Hlavní autoři: Bellemare, Marie-Josée, Bohle, D Scott, Brosseau, Colin-Nadeau, Georges, Elias, Godbout, Marianne, Kelly, Jane, Leimanis, Mara L, Leonelli, Richard, Olivier, Martin, Smilkstein, Martin
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 18.06.2009
Témata:
Animals
Female
Fluorescence
Hemeproteins - chemical synthesis
Hemeproteins - chemistry
Macrophages - chemistry
Mice
Mice, Inbred BALB C
Plasmodium falciparum - chemistry
Protoporphyrins - chemistry
Time Factors
ISSN:1520-6106
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Shrnutí:The condensed crystalline phase of iron(III) protoporphyrin IX either isolated from parasite culture as malaria pigment (hemozoin) or synthetic equivalent hematin anhydride exhibits a solid-state autofluorescence characterized by an excitation maximum of 555 nm and an emission maximum of 577 nm. The excitation spectrum maximum at 555 nm corresponds to the Q(0,0) band in the absorption spectrum which represents the lowest singlet of the material. This suggests that the fluorescent emission is due to the heme condensed phase. The photoluminescence lifetime of tau(f) = 2.7 +/- 0.8 ns as measured at four wavelengths between 550 and 600 nm is in the range of Frankel exciton in porphyrinic condensed phases. The material is shown to have an optical band gap of 2.04 eV characteristic of a semiconductor. Luminescence is markedly dependent upon the degree of hydration and the emission does not seem to be caused by presence of zinc(II) protoporphyrin IX or free-base protoporphyrin IX in the lattice. The autofluorescence can be used for in vivo tracking of hemozoin, for determination of parasitemia levels, and for infection monitoring and possibly for drug screening studies.
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ISSN:1520-6106
DOI:10.1021/jp8104375