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At least 1,261 records · Page 70Linked to original sources

Toxicity of boron to rainbow trout: a weight-of-the-evidence assessment.

From the large data set available on the toxicity of boron to aquatic organisms, the toxicity of boron to the early life stages of rainbow trout (Oncorhyncus mykiss) is the seminal issue relative to setting water quality criteria and effluent standards. Issues associated with the early life stage studies are the flat concentration-response curve, the low threshold of toxicity, and teratogenic effects observed. Recent laboratory and field studies offer new experimental data that make a weight-of-the-evidence assessment timely. In a re-examination of the effect of boron on the embryo-larval stage in rainbow trout and zebrafish, adverse effects due to boron deficiency are observed which decrease with increasing dose. It was found that low concentrations of boron stimulate embryonic growth in rainbow trout and increase the viability and survival of embryonic zebrafish. As boron concentration is further increased, the dose-response curve becomes flat as homeostatic processes are active; this is followed at higher doses by a new adverse response that increases with increasing dose. As a result, the dose-response relationship is U shaped, consistent with the characteristic shape of an essential micronutrient. Thus, effects originally reported to be toxicity at low exposures rather may be due to boron deficiency. Water analyses in trout hatcheries and field studies in wild trout streams add additional information on the toxicity of boron to trout. Of particular note is a controlled field study carried out in the Firehole River in Yellowstone Park (WY, USA), where trout populations survive and reproduction successfully occurs in natural water containing boron concentrations up to and in some cases greater than 1.0 mg B/L. Teratogenic effects due to boron exposure were not observed in any of these more recent studies.

Animals↗

[Determination of moth-proof agent residues in textiles with headspace solid-phase microextraction and gas chromatography-mass spectrometry].

A procedure is described for the identification and determination of volatile moth-proof pesticide residues, dichlorobenzene and naphthalene, in textile products by headspace solid-phase microextraction (HS-SPME) coupled with GC/MS in selective ion monitoring mode (SIM). Several standard fabrics (ISO 105/F01-1982) are used as sample matrices to reduce the target compound-matrix interaction. Prior to SPME, 0.2 g textile sample is immersed in 3 mL boric acid-citric acid-sodium acid phosphate buffer (pH 2.2) solution with 300 g/L sodium chloride and 5% (volume fraction) methanol for supersonic treatment in water bath(50 +/- 1) degrees C. Then an SPME fiber holder is used manually by passing the needle through the septum of the sample vial, depressing the plunger and lowering a fused silica fiber coated with 100 microns polydimethylsiloxane (PDMS) into the headspace right above the sample solution. Adsorption equilibrium is almost established within 5 minutes with magnetic stirring at (40 +/- 1) degrees C. After sample adsorption, draw SPME fiber into the needle, and withdraw the needle from the sample vial and immediately introduce it into the chromatograph injector, where the adsorbed analytes are thermally desorbed for 3 minutes at 230 degrees C and delivered to a capillary GC column for analysis by mass detector. The method provides data of very good linearity with low coefficients of variation for volatile target compounds like p-dichlorobenzene and naphthalene. For all the fabrics tested, typical limits of detection (LOD) were 1 microgram/kg and average recoveries from fortified sample fabrics were between 83.6%-115.2% and the relative standard deviations of the residues were 8.1%-9.8%.

English Abstract↗

[Determination of angiotensin-converting enzyme activity by micellar electrokinetic capillary chromatography].

A sensitive and rapid method was developed for angiotensin-converting enzyme (ACE) activity determination by micellar electrokinetic capillary chromatography (MECC). MECC was carried out to separate and quantify the products of the enzymatic reacting using Hip-Leu-His as the substrate in 20 mmol/L boric acid-borate buffer (pH 9.0) including 50 mmol/L SDS as the run buffer at an applied voltage of 8.1 kV. The electrophoresis was monitored at 228 nm, and completed in 6 minutes. The detection limits of ACE activity was 5 pmol/min(signal to noise ratio was 2).

Buffers↗

Chlorampenicol retention on, and penetration into, the rabbit eye.

The retention of the antibiotic chloramphenicol on, and penetration into, the rabbit eye has been compared following administration in two vehicles. Samples were taken of both aqueous humor and a washing fluid applied to the conjunctival surface and the concentration of 14C-chloramphenicol determined. Greater tear film and aqueous humor drug concentrations, which are effective against many organisms, were found with a vehicle which enhanced retention time on the ocular surfaces.

Animals↗

Determination of physostigmine and pyridostigmine in pharmaceutical formulations by capillary electrophoresis.

Physostigmine (PHY) and pyridostigmine (PYR) are two important anticholinesterase compounds with several clinical uses. Recently, PHY has been investigated for the treatment of senile dementia in Alzheimer's disease. However, both PHY and PYR have gained importance as antidotes for anticholinergic drugs. In military medicine, PYR is used as a prophylactic against nerve gas poisoning and was used in Saudi Arabia during the Gulf War in 1991. A new capillary zone electrophoresis (CZE) method for the rapid determination of PHY and PYR in pharmaceutical preparations has been developed. An untreated fused-silica capillary tube (75 microm i.d., 44 cm total length, 36.5 cm length to the detector) was employed with detection at 200 and 270 nm for PHY and PYR, respectively. The optimal separation conditions for PHY were: 50 mM boric acid-HCl buffer (pH 3.25) with 30 mM NaClO4, electrokinetic injection for 5 sec at -5 kV, temperature 25 degrees C, and separation voltage 15 kV. The optimal separation conditions for PYR were: 20 mM phosphate buffer (pH 7), electrokinetic injection for 20 sec at -10 kV, temperature 25 degrees C, and separation voltage 15 kV. The limits of detection (LOD, S/N = 3) were 70 and 60 ppb for PHY and PYR, respectively. The method can be used for the monitoring of possible main degradation products in tablets of military antidote formulations.

Chemistry, Pharmaceutical↗

[Photolysis kinetics and photoinitiated polymerization mechanism studies of [Cp-Fe-Naph]BF4 and [Cp-Fe-Cp]BF4 by UV spectrum].

The absorption spectra of photoinitiator cyclopentadiene-Fe-naphthalene tetrafluoroborate salt ([Cp-Fe-Naph]BF4) and ferocinium tetrafluoroborate salt([Cp-Fe-Cp]BF4), in two solvents have been studied. The influence of irradiation on the solution of photoinitiator has been observed. The kinetics of photolysis has been determined by real-time UV absorption spectrum. The results show that the photolysis reactions of two initiators are the first order reaction, the rate constant of photolysis reaction are 0.72 and 0.65 min-1, respectively. The photoinitiated mechanism of [Cp-Fe-Cp]BF4 was obtained.

Borates↗