Naturally occurring 1,2,8-trimethoxyxanthone and biphenyl ether intermediates leading to 1,2-dimethoxyxanthone.

In order to study structure-activity relationships, a series of mono-, di- and trioxygenated xanthones has been synthesized and the structures of methyl 2-(3,4-dimethoxyphenoxy)benzoate, C(16)H(16)O(5), 2-(3,4-dimethoxyphenoxy)benzoic acid, C(15)H(14)O(5), 1,2-dimethoxy-9H-xanthen-9-one, C(15)H(12)O(4), and 1,2,8-trimethoxy-9H-xanthen-9-one, C(16)H(14)O(5), have been determined. The first two compounds both assume skew conformations, the dihedral angles between the two phenyl rings being 80.04 (8) and 83.0 (1) degrees, respectively. The latter two compounds are essentially planar and their methoxy substituents assume orientations consistent with minimum steric interactions.

[American cutaneous leishmaniasis in the sugar cane-producing area of Pernambuco, North-East Brazil]. / La leishmaniose tégumentaire américaine dans la région sucrière du Pernambouc, Nord-Est du Brésil.

The cases of American cutaneous leishmaniasis reported here were observed between 1995 and 1998 in outpatients at a health clinic in the sugar cane-producing region in the south of Pernambuco State (Brazil), in which the disease is known to be endemic. Two hundred thirty eight cases were reported, equivalent to about ten cases per thousand patients. The disease affected patients of all ages, with a slight male predominance. The lesions were generally single and located on the legs. They were successfully treated with Glucantime. Vectors of the disease, sandflies of the genus Lutzomyia, were captured in and around homes, particularly in stables. This field work demonstrates the extent of a long-standing endemic that can be effectively treated within motivated health structures.

Umbilical cord blood processing with the Optipress II blood extractor.

BACKGROUND: We have previously shown that UC blood (UCB) units can be volume-reduced manually, in a closed system, without major losses of nucleated and CD34(+) cells and without the addition of exogenous material. Our aim was to use an automated method for the separation of the UCB components using the Optipress II, extractor, with the 'buffy-coat' collection in a standardized volume. METHODS: After centrifugation, the 51 UCB units were separated into the three blood components, plasma, buffy coat (BC) and red cells, using the Optipress II. The final volume of the BC fraction, rich in nucleated and progenitor CD34(+) cells, was set at 30 mL. The nucleated and CD34(+) cell content of the UCB collections and the resulting BC were evaluated. RESULTS: The UCB units were grouped according to the volume collected: Group I < 80 mL and Group II > or = 80 mL. Standardization of the BC at 30 mL resulted in significant volume reduction for both groups, with median values of 51% in Group I and 70% in Group II. The nucleated and CD34(+) cell recoveries in the BC from Group I were 88% and 99% respectively; for Group II they were 80% and 97%. DISCUSSION: This semi-automated method of volume reduction efficiently reduces low, as well as high volume UCB units, with good nucleated- and progenitor-cell yields. Being a closed system and free of external material, the risk of contamination is minimized. The resulting fractions are then available for validation studies of the unit, effectively fulfilling the main requisites for UCB banking.

Analysis of surface markers on CD34+ cells, isolated from cord blood and G-CSF primed peripheral blood.

We report a comparative study of the expression of multilineage and adhesion molecules on CD34+ cells isolated from human umbilical cord blood (CB) and G-CSF-mobilized peripheral blood progenitor cells (PBPC) from healthy volunteers. The major difference found between the two sources of CD34+ populations was the expression of CD54 molecule, which was higher in CB in comparison to PBPC.

Umbilical cord blood processing: volume reduction and recovery of CD34+ cells.

One of the main problems for the establishment of umbilical cord blood (UCB) banks is the storage space needed for the frozen samples. The aim of this study was to find a method of reducing the volume of UCB units without major losses of the haematopoietic progenitor-CD34+ cells. The UCB was collected into a triple blood bag system, in which the anti-coagulant had been previously adjusted. The blood bag was first centrifuged for red cell depletion followed by a second centrifugation for plasma reduction. At this point, the main bag containing the white blood cell (WBC) rich fraction "buffy coat' (BC) and the "waste bag' were sealed and detached. Haematologic cell counts and CD34+ cell quantification were done in whole blood and in the isolated fractions. The average volume of the 19 UCB samples processed was 103 ml. Separation by centrifugation led to a mean volume reduction of 56% with red cell depletion of 59%. The white blood cell recovery was of 72% with a significant CD34+ cell recovery of 87%. This seems a promising method for cord blood volume reduction and enrichment of CD34+ cells.