Disease relevance of Killvermyl

• Bromothymol blue (B) broth for the cultivation, detection, and identification of Ureaplasma urealyticum is described [1].
• Bromothymol blue broth: improved medium for detection of Ureaplasma urealyticum (T-strain mycoplasma) [1].
• The addition of 0.001% bromocresol purple and 0.001% bromothymol blue to buffered charcoal-yeast extract agar allowed differentiation between members of the family Legionellaceae [2].
• The bromothymol blue test was less sensitive than the California Mastitis Test but offered several practical advantages for use on farm [3].
• Detection of bovine mastitis by bromothymol blue pH indicator test [3].

High impact information on Killvermyl

• D-Sorbitol, as the main carbon source, differentiates the species that can ferment it by the pH indicators cresol red and bromothymol blue [4].
• For primary isolation on genital mycoplasma agar 95% N2-5% CO2 gave 100% correlation with growth in bromothymol blue broth, whereas certain strains failed to grow on agar incubated in air, the TABCO2 system (Lab-Tek Division, Miles Laboratories, Ltd., Rexdale, Canada), 100% CO2, or under anaerobiosis [5].
• The difference in pH of the sample in the presence and absence of formaldehyde, which blocks the amino function, provides the value of r.a.n. by monitoring the changes in absorbance of bromothymol blue at 616 nm [6].
• 1. During aerobic cation uptake in liver mitochondria, the hydrophobic pH indicator bromothymol blue undergoes a multiphase response: phase 1 (rapid acidification), phase 2 (slow alkalinization), phase 3 (rapid alkalinization) and phase 4 (reacidification) [7].
• The change in pH was demonstrated by spectral changes of the pH indicators Bromocresol Green, Bromothymol Blue, Bromocresol Purple and Phenol Red. The magnitude of the pH change was calculated from the kinetics of the changes in the indicators' absorbance and from fluorescence intensity of naphtholate [8].

Chemical compound and disease context of Killvermyl

• A synthetic basal salts medium containing inositol as the sole source for carbon and energy and bromothymol blue as pH indicator, selectively supports the growth of Klebsiella pneumoniae and Serratia spp [9].

Anatomical context of Killvermyl

• Glyco- and tauro-deoxycholate induce alkalinization of the intra-mitochondrial space as determined on bromothymol blue pre-loaded mitochondria [10].
• Bromothymol blue as a probe for structural changes of model membranes induced by hemoglobin [11].
• The inhibition by bromothymol blue of anion translocation across the mitochondrial membrane [12].
• Stable liposome-type artificial red blood cells containing either an aqueous bromothymol solution or erythrocyte haemolysate were produced using carboxymethylchitin as a stabilizer [13].
• Sensitivity, specificity, positive predictive value and negative predictive value of each test were as follows, respectively: IGFBP-1 (86, 74, 73 and 87%); bromothymol (64, 100, 100 and 77%); fern test (62, 96, 93 and 75%) and ultrasonography (19, 100, 100 and 61%) [14].

Associations of Killvermyl with other chemical compounds

• Both hydrophilic bromothymol blue and lipophilic dapsone were encapsulated in these liposomes and their in vitro release studies were carried out at 37 degrees C using different media, namely, phosphate buffer (pH 7.4), 0.02 N-HCl and 1% mouse plasma [15].
• Differentiation of Cryptococcus neoformans serotypes A and D using creatinine dextrose bromothymol blue thymine medium [16].

Analytical, diagnostic and therapeutic context of Killvermyl

• The drug was determined with bromothymol blue at pH 9.0, using one extraction in the direct procedure and 2 successive extractions in the combined elution-extraction process after thin layer chromatography [17].

References