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At least 937 records · Page 52Linked to original sources
PubMed1980

[Therapy of juvenile iron deficiency with bivalent iron dragees (Fe2-fumarate, succinate, sulfate). Controlled double-blind study].

In 53 children with moderate iron deficiency (haemoglobin 7,5 to 12 g/dl) divalent iron salts as tablets (59Fe2+-fumarate, -succinate, -sulfate) were tested versus placebo (controlled double-blind study). Gastrointestinal side effects were most frequently seen with iron succinate (50%) and iron sulfate (25%). Therapeutic success as measured by haemoglobin regeneration was not significantly different among the three iron salts, but significantly more effective than in the placebo group. Children beyond the age of two years mostly refused the application of tablets and should be supplied with liquid preparations.

Anemia, Hypochromic↗
PubMed1994

[Microbiological consequences of chelation of bivalent metal cations by nitroxoline].

The present work deals with the physico-chemical and microbiological investigations made in order to explain the role of divalent cations in the mechanism of the action of nitroxoline (NIT), an antibiotic used in the treatment of uncomplicated urinary tract infections. Preliminary studies reported that bacteriostatic and bactericidal activities of NIT on Escherichia coli strains are decreased in the presence of Mg2+ and Mn2+ but not with Ca2+. A spectrophotometric study, conducted in order to elucidate the interaction between metal ions and NIT, showed the formation of drug-metal ion complexes. In addition, we examined the relationships between the metal ions-chelating property of NIT and its effects on the decrease of the mannose sensitive hemagglutination titer and the production of siderophores from E. coli. The results suggested that these antimicrobial activities of NIT would also be due to the complexation of metal ions by this molecule.

Anti-Infective Agents, Urinary↗
PubMedDate not supplied

[The determination of the optimal inoculation dose of an oral cholera bivalent chemical vaccine in a controlled trial of the vaccination of children and adolescents].

The reactogenicity and immunological effectiveness of different doses of cholera vaccine for oral administration (in tablets), containing choleragen toxoid, Ogawa and Inaba O-antigens and some of Vibrio cholerae exoenzymes, have been tested on 143 children aged 2-17 years. In this investigation the optimum immunization doses of the preparation have been established: two tablets containing 100,000 binding units (BU) of the toxoid and 2,500 units of O-antigen for children 11-14 years; four tablets containing 200,000 BU of the toxoid and 5,000 units of O-antigen for adolescents aged 15-17 years. An essential advantage of the oral vaccine over vaccines intended for parenteral administration lies in its capacity for inducing the accumulation of secretory antibodies (coproantibodies) in practically all vaccinees.

Administration, Oral↗
PubMedDate not supplied

[The use of a live Salmonella bivalent vaccine for decreasing the circulation of salmonellae in a poultry plant].

S. typhimurium (expressing antigen 09 of S.dublin) recombinant vaccine strain was tested at a large poultry-breeding farm under the conditions of permanent circulation of salmonellae. The oral immunization of laying hens in three administrations with doses of 5 x 10(8), 5 x 10(9) and 5 x 10(9) microbial cells induced an increase in titers of antibodies only to group D salmonellae, while in immunized chickens (each receiving a dose of 3 x 10(8) microbial cells) antibodies to both group B and group D salmonellae were detected. The vaccination of laying hens and chickens produced a protective effect due to the development of immunity and the decrease of Salmonella contamination of eggs laid by immunized hens, thus reducing the risk of infection at incubator stations. Total mortality during the first 3 months of life was essentially lower (p < 0.001) among immunized chickens (4.41 +/- 0.09%) than in the control group of nonimmunized chickens (5.91 +/- 0.10%).

Administration, Oral↗
PubMed1997

Potential of protein OprF of Pseudomonas in bivalent vaccines.

Outer membrane protein OprF is the major outer membrane of Pseudomonas aeruginosa, and has been expressed to a similar high level in Escherichia coli from the cloned gene. It contains conserved surface epitopes, and antibodies against these epitopes can protect mice from P. aeruginosa infections. To develop the oprF gene as a carrier for foreign epitopes, linker insertion mutagenesis has been performed to introduce 12 nucleotide inserts marked by a unique PstI site. Nine such sites can accept and express a foreign epitope within the surface loop regions of OprF on the surface of E. coli. The antigenicity at a given insertion site, and the influence of the length of a model repeating malarial epitope on antigenicity, have been shown to be site-specific and apparently dependent on the nature of the surrounding amino acids at the insertion site. Immunization of mice with OprF containing a highly antigenic inserted epitope led to an epitope-specific antibody response. These data suggest that OprF has potential for use as a carrier for foreign epitopes.

Amino Acid Sequence↗
PubMed1976

[Production and testing of a live lyophilized bivalent vaccine against Aujeszky's disease and erysipelas in swine].

A live freeze-dried bivaccine against swine erysipelas and Aujeszky's disease in pigs was produced, its antigen titers reaching 10(8) and 10(4.67) for the two components, respectively. The immunity conferred to the vaccinated pigs (so far as Aujeszky's disease is concerned) had an antibody titer of 1:4, and in sheep the titer was up to 1:16, these animals showing resistance at a control infection with 5000 LD50 per head. The vaccinated pigs likewise withstood a control infection with a mixed 24-48-hour broth culture of virulent strains causing swine erysipelas.

Animals↗
PubMed1998

Biodistribution and dosimetric study in medullary thyroid cancer xenograft using bispecific antibody and iodine-125-labeled bivalent hapten.

UNLABELLED: The purpose of this study was to evaluate biodistributions and absorbed doses of anti-carcinoembryonic antigen (CEA)/anti-diethylenetriamine pentaacetic acid (DTPA)-indium (anti-DTPA-In) bispecific monoclonal antibody (BsMAb) F6-734 and 125I-labeled DTPA-indium dimer hapten (125I-di-DTPA-In hapten) in athymic mice xenografted with human medullary thyroid cancer. METHODS: Bispecific monoclonal antibodies F6-679 (anti-CEA/antihistamine) and G7A5-734 (antimelanoma/anti-di-DTPA-In) were used as irrelevant BsMAbs. Athymic mice inoculated with TT medullary thyroid cancer cells expressing CEA were administered BsMAbs F6-734, F6-679 or G7A5-734 and then, 48 hr later, 125I-di-DTPA-In hapten. Iodine-125-labeled F6 F(ab')2 fragment was injected into other groups of mice. Biodistributions were examined at 30 min and 5, 24, 48 and 96 hr after injection of 125I-di-DTPA-In hapten or 125I-labeled F6 F(ab')2. RESULTS: In mice injected with BsMAb F6-734 and 125I-di-DTPA-In hapten, tumor uptake was 9.1%+/-2.1%, 8.7%+/-3.5%, 8.0%+/-2.3%, 5.1%+/-0.9% and 3.5%+/-1.5% of the injected dose/g at 30 min and 5, 24, 48 and 96 hr, and tumor-to-blood, tumor-to-liver and tumor-to-kidney ratios were 37.0+/-12.5, 32.3+/-10.9 and 10.4+/-2.7 at 24 hr. Iodine-125-F6 F(ab')2 fragment showed a tumor uptake of 7.39% injected dose/g and tumor-to-blood, tumor-to-liver and tumor-to-kidney ratios of 1.8+/-0.6, 7.3+/-2.9 and 3.6+/-1.6 at 24 hr. In mice injected with F6-679 or G7A5-734, tumor uptake and tumor-to-normal tissue ratios were much lower than in the mice injected with F6-734. These results were confirmed by autoradiographic studies that demonstrated clear tumor-to-normal tissue contrast. CONCLUSION: This two-step targeting method seems very potent for the diagnosis and therapy of human medullary thyroid cancer and other CEA-producing tumors because it combines high tumor uptake and low normal tissue background.

Animals↗
PubMed1996

Effect of Sandimmun Neoral on the level of bivalent cations in erythrocytes of kidney transplant recipients.

In a 4 month study, a group of 16 patients with stable renal graft function receiving triple immunosuppressive therapy including cyclosporin A (Cy A) were investigated for the levels of calcium, magnesium and zinc in erythrocytes. The patients were randomized to be converted to the new microemulsion formulation (Sandimmun Neoral) in a 1:1 fashion (n = 8) or to continue with the classical formulation (Sandimmun) (n = 8). The concentrations of creatinine, phosphate, alkaline phosphatase activity, calcium, magnesium and zinc were measured twice a month in blood plasma. The concentration of calcium, magnesium and zinc in erythrocytes was also measured. The concentration of magnesium in blood plasma and erythrocytes during the study showed no deviation from normal values. The level of zinc in erythrocytes was almost twice as high as in normal healthy controls and was not dependent on Cy A formulation. Calcium content in erythrocytes of patients receiving Sandimmun was 27.6% higher than in healthy persons. Conversion of the patients to Sandimmun Neoral normalized the calcium concentration in erythrocytes and caused a transient increase of calcium levels in blood plasma.

Administration, Oral↗
PubMed1981

Fine structure and behaviour of a pericentric inversion in the sand rat, Psammomys obesus.

In pachytene spermatocytes of the sand rat, Psammomys obesus, a long autosomal bivalent was observed, which was asynaptic for a large interstitial segment of its length in early pachytene. This bivalent also exhibited unaligned kinetochores. In late pachytene spermatocytes all autosomal bivalents were fully synapsed, but one of the shortest bivalents now possessed unaligned kinetochores. Evidence is presented in support of the proposition that the asynaptic interstitial region observed in early pachytene is due to the bivalent being heterozygous for a pericentric inversion. Using the maximum extent of homologous pairing, the break points were mapped at 26% from one end and 20% from the other. The unaligned kinetochores support the proposal that the aberration is an inversion and measurements of their positions confirm the estimated break points. In one cell a bivalent with interstitial (but no terminal) synapsis also confirms the inversion hypothesis. It is proposed that the bivalent is so small that topological considerations prevent the formation of the expected inversion loop. Evidence is also presented that complete synapsis of the bivalent during late pachytene can be attributed so 'synaptic adjustment', characterized by non-homologous synapsis (heterosynapsis). The position of the aberrant bivalent in relation to the sex chromosomes also changes during pachytene. When the bivalent is incompletely synapsed it generally associates by its ends with the ends of the sex chromosomes, but when it is non-changes during pachytene. When the bivalent is incompletely synapsed it generally associates by its ends with the ends of the sex chromosomes, but when it is non-homologously synapsed it is not associated with them.

Animals↗