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Chemical Compound Review

lead; sulfane     lead; sulfane

Synonyms: AG-F-39132, AC1O4DFS, CTK1C4101, hydrogen sulfide; lead
 
 
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Disease relevance of LEAD SULFIDE

  • Although the histological and biochemical responses to lead toxicity were restricted to the more soluble lead compounds in this study, lead from Skagway lead ore concentrate and lead sulfide was also bioavailable, and accumulated in proportion to dose in vulnerable target organs such as bone and kidney [1].
  • Pneumoconioses produced by intratracheal applications of various dusts (quartz, coal, cadmium and lead sulfide) in rats were investigated by electron microscopy in order to follow the pathway of the dust particles from the alveoli into the pulmonary interstitium [2].
 

High impact information on LEAD SULFIDE

  • Three-dimensional, orthogonal lead sulfide (PbS) nanowire arrays and networks have been prepared by using a simple, atmospheric pressure chemical vapor deposition (APCVD) method [3].
  • However, in all field samples, (sub)nanomolar levels of acid-leachable sulfide were recovered at pH 5.0-6.2, which could be attributed to dissociation of lead sulfide complexes with moderate acidity [4].
  • Extended X-ray adsorption fine structure (EXAFS) and X-ray absorption near edge structure (XANES) spectroscopy data indicated that lead sulfide was greater after 99 d in the treatments that included additions of sulfate [5].
  • Enzyme reaction product, lead sulfide, was localized to lysosomal organelles in normal platelets, and only in rare examples appeared in the DTS [6].
  • Comparison of lead bioavailability in F344 rats fed lead acetate, lead oxide, lead sulfide, or lead ore concentrate from Skagway, Alaska [1].
 

Biological context of LEAD SULFIDE

 

Associations of LEAD SULFIDE with other chemical compounds

 

Analytical, diagnostic and therapeutic context of LEAD SULFIDE

References

  1. Comparison of lead bioavailability in F344 rats fed lead acetate, lead oxide, lead sulfide, or lead ore concentrate from Skagway, Alaska. Dieter, M.P., Matthews, H.B., Jeffcoat, R.A., Moseman, R.F. Journal of toxicology and environmental health. (1993) [Pubmed]
  2. Electron microscopic investigations on dust penetration into the pulmonary interstitium in experimental pneumoconioses. Kissler, W., Morgenroth, K., Scherbeck, W. Respiration; international review of thoracic diseases. (1982) [Pubmed]
  3. Orthogonal PbS nanowire arrays and networks and their raman scattering behavior. Ge, J.P., Wang, J., Zhang, H.X., Wang, X., Peng, Q., Li, Y.D. Chemistry (Weinheim an der Bergstrasse, Germany) (2005) [Pubmed]
  4. Determination of Pb complexation in oxic and sulfidic waters using pseudovoltammetry. Rozan, T.F., Luther, G.W., Ridge, D., Robinson, S. Environ. Sci. Technol. (2003) [Pubmed]
  5. Metal bioavailability and speciation in a wetland tailings repository amended with biosolids compost, wood ash, and sulfate. DeVolder, P.S., Brown, S.L., Hesterberg, D., Pandya, K. J. Environ. Qual. (2003) [Pubmed]
  6. Localization of a lysosomal enzyme in platelets from patients with the White platelet syndrome. White, J.G. Platelets (2006) [Pubmed]
  7. Light microscopical localization of enzymes by means of cerium-based methods. III. Visualization techniques for cerium phosphate. Halbhuber, K.J., Zimmermann, N., Feuerstein, H. Acta Histochem. (1985) [Pubmed]
  8. Investigations of urinary stone formation following persorption. Brosig, W., Rost, A., Riedel, B. Transactions of the American Association of Genito-Urinary Surgeons. (1976) [Pubmed]
  9. Features of the cerebral vascular pattern that predict vulnerability to perfusion or oxygenation deficiency: an anatomic study. Moody, D.M., Bell, M.A., Challa, V.R. AJNR. American journal of neuroradiology. (1990) [Pubmed]
  10. Fluorescence spectroscopy of single lead sulfide quantum dots. Peterson, J.J., Krauss, T.D. Nano Lett. (2006) [Pubmed]
 
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