triethyllead and trimethyllead

A method for the extraction of triethyl lead (TEL(+)), trimethyl lead (TML(+)), and Pb(2+) from sand was developed using supercritical modified CO(2)-CH(3)OH extraction and in situ complexation with sodium diethyldithiocarbamate (NaDDTC) using a 2(5) factorial exploratory design is described. The screened variables were (i) pressure (69-193 bar), (ii) temperature (40-150 degrees C), (iii) ligand amount (0-100 mg), (iv) methanol volume (0.0-0.5 mL) and (v) static time (0-45 min). The optimum extraction conditions found were as follow: pressure, 193 bar; temperature, 40 degrees C; amount of NaDDTC, 100 mg; methanol volume, 0.5 mL; static time 45 min; and CO(2) flow rate, 1 mL min(-1). Under these conditions the following recoveries were obtained (TML(+) 97+/-2%, TEL(+) 70+/-5%, and Pb(2+) 100+/-4%). The presence of NaDDTC is not necessary for the extraction of TML(+) and TEL(+), but it is a very significative parameter for Pb(2+). A second experimental design 2(2)+star for temperature and pressure was realized, but the results were not better than those of the first model. SFE extract derivatization was achieved with pentylmagnesium bromide, and target analyte determination was carried out by gas chromatography-mass spectrometry. Detection limits in the full-scan mode were 4, 10, and 39 pg as lead for TMPeL, TEPeL and PbPe(4), respectively. The method was validated with urban dust containing TML(+) (CRM 605. Pb 7.9 +/-1.2 microg kg(-1)) and river sediment containing inorganic lead (GBW08301. Pb 79.0+/-12.0 mg kg(-1)) as reference materials. The proposed method was applied to lead analysis in sand collected from an oil-polluted beach in Chile.

Topics: Analytic Sample Preparation Methods; Chromatography, Supercritical Fluid; Ditiocarb; Environmental Monitoring; Gas Chromatography-Mass Spectrometry; Geologic Sediments; Lead; Methanol; Organometallic Compounds; Reproducibility of Results; Temperature; Tetraethyl Lead; Water Pollutants, Chemical

The interactions of the tributyl, triethyl and trimethyllead compounds with energized mitochondria have been investigated in this paper. It has been shown that the (alkyl)(3)Pb-Cl compounds induce swelling in mitochondria suspended in a sucrose medium. The phenomenon is more marked the higher the lipophilicity and occurs in the following order: (Bu)(3)Pb>(Et)(3)Pb>(Me)(3)Pb. As swelling is inhibited by cyclosporine, this suggests that the swelling is due to the opening of a trans-membrane pore (MTP pore) in the mitochondria. As this pore can be responsible for the inhibition of the ATP synthesis, and, consequently for cell death, the opening of the pore could be one of the reasons for the toxicity of the (alkyl)(3)Pb-X compounds.

Topics: Animals; Mitochondria, Liver; Mitochondrial Membranes; Organometallic Compounds; Rats; Spectrophotometry, Ultraviolet; Tetraethyl Lead

One analytical procedure for the determination of ionic alkyllead in human urine has been studied. The system consists of the extraction of Me3Pb+, Et3Pb+ and Pb2+ at pH 9.0 with diethyldithiocarbamate to an organic phase. Then, the ionic compounds are butylated with BuMgCl and the final organic solution is analyzed by GC-MS-SIM. The elimination of both foam and gels in the extraction step and the general procedure for the urine are discussed. The recovery of compounds ranges from 105.1% for Me3Pb+ to 97.2% for Et3Pb+ using hexane as extracting agent and detection limits are 18.4 pg/ml of Me3Pb+ and 19.2 pg/ml of Et3Pb+ in urine. The speciation of ionic alkylleads in the urine of a petrol station worker showed a value of 27.9 pg/ml of Me3Pb+ in urine and Et3Pb+ was below the detection limit.

Topics: Ethanol; Gas Chromatography-Mass Spectrometry; Humans; Indicators and Reagents; Lead; Organometallic Compounds; Pentanes; Pentanols; Tetraethyl Lead

The effect of organic lead and tin compounds upon the integrity of cerebral neurotubules has been studies in vitro and in vivo, using 3H-colchicine binding as an index of tubulin aggregation. Triethyl tin, trimethyl lead and triethyl lead chlorides at concentrations above 5 X 10(-5)M, all prevented the polymerization of tubulin. Inorganic lead had a similar effect. Trimethyl tin had a much lesser capacity to prevent such polymerization. Rats received a single dose of each organometal, by subcutaneous injection and the capacity of hippocampal soluble protein to bind 3H colchicine was assessed. At organometal doses sufficient to cause morphological damage and behavioral change, no significant differences of colchicine binding capacity were apparent.

Topics: Animals; Brain; Lead; Male; Microtubules; Organometallic Compounds; Rats; Rats, Inbred F344; Tetraethyl Lead; Triethyltin Compounds; Trimethyltin Compounds; Tubulin

The dose-related behavioral effects produced by triethyl (TEL) (2.6 to 7.9 mg/kg) and trimethyl lead (TML) (8.8 to 26.2 mg/kg) were assessed 2, 7, 14, 21 and 28 days following injection. TEL, but not TML, produced dose- and time-related decreases in body weight. Both agents decreased vertical and horizontal components of motor activity 2 days postdosing; increased activity was seen consistently in TEL-exposed rats 7 to 21 days after dosing. TML increased fore- and hindlimb strength for up to 28 days postdosing. TEL had no consistent effect on this measure. Both TEL and TML decreased responsiveness to an acoustic stimulus during the first two weeks postdosing. Latency to respond to a thermal stimulus was increased 2 to 14 days after TEL with the peak change occurring from 2 to 7 days. The peak of effect following TML was two weeks postdosing. In general, there was a significant correlation between both TEL and TML-induced changes in blood and brain lead levels and decreased sensitivity to a thermal stimulus. The apparent delayed onset of TML-induced neurobehavioral effects may be related to a longer time to obtain peak blood or brain levels. Histopathological assessment of rats 7 or 28 days after TEL and TML indicated that TEL caused structural abnormalities in the hippocampus and dorsal root ganglion, while TML produced changes primarily in the spinal cord and brain stem.

Topics: Animals; Behavior, Animal; Body Weight; Brain; Dose-Response Relationship, Drug; Male; Motor Activity; Organometallic Compounds; Rats; Rats, Inbred F344; Reaction Time; Reflex, Startle; Sensory Thresholds; Spinal Cord; Tetraethyl Lead

Recent reports have demonstrated that organolead and -tin compounds can alter behavioral reactivity to noxious stimuli. To further define the dose response and temporal characteristics of these neurobehavioral effects, male Fischer 344 rats were injected sc with either one-fourth, one-half, or three-fourths the acute LD50 of triethyl lead (TEL), triethyl tin (TET), trimethyl lead (TML), trimethyl tin (TMT), or distilled water and tested on a 57.5 degrees C hot plate 1, 7, 14, 21, and 28 days after dosing. All four organometals altered hot plate latencies, but the magnitude and time course of these effects differed among the compounds. TEL produced a dose-related increase in latencies which was maximal 1 and 7 days postdosing and had dissipated by 28 days. In contrast, the group administered TML (3/4 LD50) exhibited a late developing antinocioception which became evident 14 days after dosing and persisted throughout the period of testing. The intermediate dose of TMT (1/2 LD50) also produced a delayed increase in response times which was observed 21 and 28 days post-treatment. The 3/4 LD50 dose of TMT produced increased hot plate latencies on all post-treatment test days except Day 14. TET (1/2 LD50) produced increased hot plate latencies 1, 7, 14, and 21 days postdosing and also induced a reversible ataxia and akinesia. Higher doses of TET proved lethal to 80% of the animals and lower doses failed to alter response times in the hot plate. These data demonstrate that trialkyl lead and tin compounds can produce time- and dose-related increases in hot plate latencies.

Topics: Animals; Central Nervous System Diseases; Dose-Response Relationship, Drug; Lead; Lead Poisoning; Lethal Dose 50; Male; Organometallic Compounds; Organotin Compounds; Pain; Rats; Rats, Inbred F344; Reaction Time; Tetraethyl Lead; Time Factors; Triethyltin Compounds; Trimethyltin Compounds

Topics: Administration, Oral; Animals; Chlorides; Lead; Lead Poisoning; Organometallic Compounds; Rats; Tetraethyl Lead