Results 191 to 200 of about 41,111 (239)
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Polymyxin B and Colistin

New England Journal of Medicine, 1964
GRAM-negative bacilli, in particular pseudomonas species, are of increasing concern to the clinician as infectious and therapeutic problems.1 , 2 Accordingly, polymyxin B has grown to singular importance as its utility to the treatment of systemic infections caused by pseudomonas species has been appreciated and exploited.
N M, NORD, P D, HOEPRICH
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Polymyxin-B-binding sites in the cochlea as demonstrated by polymyxin-B/gold labeling

Histochemistry, 1986
A polymyxin-B/bovine-serum-albumin/gold complex was used as a probe to detect the binding sites of polymyxin B on thin sections of cochlea embedded in Spurr's resin. The binding sites were found to be mainly located on the stereocilia, the cuticular plate of hair cells, the head plate of Deiters' cells, the tonofilaments in pillar cells and Deiters ...
M, Tachibana   +3 more
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Polymyxin B: similarities to and differences from colistin (polymyxin E)

Expert Review of Anti-infective Therapy, 2007
Hospital-acquired infections due to multidrug-resistant gram-negative bacteria constitute major health problems, since the medical community is continuously running out of available effective antibiotics and no new agents are in the pipeline. Polymyxins, a group of antibacterials that were discovered during the late 1940s, represent some of the last ...
Andrea, Kwa   +3 more
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Clinical Use of Polymyxin B

2019
Polymyxin B is another clinically available polymyxin that has re-emerged in clinical practice to treat infections caused by multi-drug (MDR) or extensively-drug-resistant (XDR) Gram-negative bacteria (GNB). Its chemical structure is very similar to the structure of polymyxin E (colistin).
Maria Helena, Rigatto   +2 more
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Studies of the biosynthesis of polymyxin B

Biochimica et Biophysica Acta (BBA) - General Subjects, 1968
Abstract Polymyxin B, a polypeptide antibiotic produced by Bacillus polymyxa, is synthesized towards the end of the exponential growth phase of the organism. Radioactive diaminobutyric acid is taken up by the cells and incorporated into the antibiotic and into other basic peptides.
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Peptide Antibiotics (Polymyxin B and Polymyxin E)

1978
Of the five polymyxins, A, B, C, D and E, originally isolated from a spore-bearing bacillus called variously B. aerosporus and B. polymyxa (Garrod et al., 1973), only two have found clinical usefulness, namely polymyxin B, usually in the form of the sulphate, and polymyxin E (colistin), either as the sulphate or sodium sulphomethate.
A. P. Ball, J. A. Gray, J. McM. Murdoch
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Prolonged Treatment with Polymyxin B

New England Journal of Medicine, 1960
BECAUSE polymyxin B has significant toxic potentialities its use is sharply circumscribed, and prolonged therapy with it is avoided. This report describes an unusual case in which circumstances necessitated the administration of polymyxin B for almost one year to a patient with a single functioning kidney.
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B‐Cell Activating Properties of Polymyxin B

Scandinavian Journal of Immunology, 1978
Polymyxins are known to be inhibitors of certain polyclonal B cell activators such as lipopolysac‐charide and dextransulphate. However, increased specific responses to hapten‐coupled mitogens have been reported after the addition of polymyxins to superoptimal conjugate doses.
C I, Smith, L, Hammarström
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The Functional Association of Polymyxin B with Bacterial Lipopolysaccharide Is Stereospecific:  Studies on Polymyxin B Nonapeptide

Biochemistry, 2000
The Gram-negative bacterial endotoxin lipopolysaccharide (LPS) is a major inducer of sepsis. The natural cyclic peptide polymyxin B (PMB) is a potent antimicrobial agent, albeit highly toxic, by virtue of its capacity to neutralize the devastating effects of LPS. However, the exact mode of association between PMB and LPS is not clear. In this study, we
H, Tsubery   +3 more
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Contact dermatitis to polymyxin B

Contact Dermatitis, 2008
M M, Jiaravuthisan, J G, DeKoven
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