Nano-intercalated rhodanese in cyanide antagonism

References

• Ashani MR, Mohri M, Chekani M. 2006. Effects of garlic (Allium sativum) and its chief compound, allicin, on acute lethality of cyanide in rat. Comp Clin Pathol 15:211–213.
   Google Scholar
• Baskin SI, Porter DW, Rockwood GA, Romano JA, Patel HC, Kiser RC, Cook CM, Ternay AL. 1999. In vitro and in vivo comparison of sulfur donors as antidotes to acute cyanide intoxication. J Appl Toxicol 19:173–183.
   PubMed Web of Science ®Google Scholar
• Block E. 1985. The chemistry of garlic and onions. Sci Am 252:94–99.
   Web of Science ®Google Scholar
• Budai M, Szabó ZS, Zimmer A, Szõgyi M, Gróf P. 2004. Studies on molecular interactions between nalidixic acid and liposomes. Int J Pharm 279:67–79.
   PubMed Web of Science ®Google Scholar
• Dagani R1996. Chemists explore potential of dendritic macromolecules as functional materials. Chem Eng News 1–13.
   Google Scholar
• Dixon WJ. 1965. The up-and-down method for small animal samples. Am Stat Assoc J 12:967–978.
   Google Scholar
• Frankenberg L. 1980. Enzyme therapy in cyanide poisoning: Effect of rhodanese and sulfur donors. Arch Toxicol 45:315–323.
   PubMed Web of Science ®Google Scholar
• Iciek M. 2001. Biosynthesis and biological properties of compounds containing highly reactive, redused sulfane sulfur. Pol J Pharmacol 53:215–225.
   PubMedGoogle Scholar
• Iciek M, Bilska A, Ksizek L, Srebro Z, Wlodek L. 2005. Allyl disulfide as donor and cyanide as acceptor of sulfane sulfur in mouse tissues. Pharmacol Rep 57:212–218.
   PubMedGoogle Scholar
• Ihler GM, Glew RH, Schnure FW. 1973. Enzyme loading erythrocytes. Proc Natl Acad Sci USA 70:2663–2666.
   PubMed Web of Science ®Google Scholar
• Katchalski E, Silman I, Goldman R. 1971. Effects of the microenvironment on the mode of action of immobilized enzymes. Adv Enzymol Mol Biol 34:445–536.
   PubMedGoogle Scholar
• Litchfield JT, Wilcoxon F. 1949. A simplified method of evaluating dose-effect experiments. J Pramacol Exp Ther 96:99–113.
   PubMed Web of Science ®Google Scholar
• Petrikovics I, Pei L, McGuinn WD, Cannon EP, Way JL. 1994. Encapsulation of rhodanese and organic thiosulfonates by mouse erythrocytes. Fund Appl Toxicol 23:70–75.
   PubMedGoogle Scholar
• Petrikovics I, Cannon EP, McGuinn WD, Pei L, Way JL. 1995. Cyanide antagonism with organic thiosulfonates and carrier red blood cells containing rhodanese. Fund Appl Toxicol 24:1–8.
   PubMedGoogle Scholar
• Petrikovics I, Papahadjapoulos D, Hong K, Cheng TC, Baskin SI, Jiang J, Jaszberenyi JC, Logue BA, Szilasi M, McGuinn WD, Way JL. 2004. Comparing therapeutic and prophylactic protection against the lethal effect of paraoxon. Toxicol Sci 77:258–262.
   PubMed Web of Science ®Google Scholar
• Petrikovics I, Wales ME, Jaszberenyi JC, Budai M, Baskin SI, Szilasi M, Logue BA, Chapela P, Wild JR. 2007. Enzyme-based intravascular defense against organophosphorus neurotoxins: Synergism of dentritic-enzyme complexes with 2-PAM and atropine. Nanotoxicology 1:1–9.
   Google Scholar
• Sayed-Sweet Y, Hedstrand DM, Spindler R, Tomalia DA. 1997. Hydrophobically modified poly(amidoamine)(PAMAM) dendrimers: Their properties at the airwater interface and useas nanoscopic container molecules. J Mater Chem 7:1199–1205.
   Web of Science ®Google Scholar
• Silbert JA. 1983. The storage of washed human erythrocytes in a protein free medium. Transfusion 23:8–10.
   PubMed Web of Science ®Google Scholar
• Tomalia DA, Baker H, Dewald J, Hall M, Kallos G, Martin S, Roeck J, Ryder J, Smith P. 1985. A new class of polymers-starburst-dendritic macromolecules. Polym J 17:117–132.
   Web of Science ®Google Scholar
• Tomalia DA, Baker H, Dewald J, Hall M, Kallos G, Martin S, Roeck J, Ryder J, Smith P. 1986. Dendritic macromolecules: Synthesis of starburst dendrimers. Macromolecules 19:2466–2468.
   Web of Science ®Google Scholar
• Tomalia DA, Naylor AM, Goddard WA. 1990. Starburst dendrimers: Molecular level control of size, shape, surface chemistry, topology and flexibility from atoms to macroscopic matter. Angew Chem Int Ed Engl 29:138–175.
   Web of Science ®Google Scholar
• Tomalia DA, Dvornic PR, Uppuluri S, Swanson DR, Balogh L. 1997. Skeletal macromolecular isomerism: A comparison of dendritic polymer properties to those of classical macromolecular architectures. Polymer Mater Sci Eng 77:95–96.
   Google Scholar
• Tomalia DA, Esfand R. 1997. Dendrons, dendrimers and dendrigrafts. Chem Ind 11:416–420.
   Google Scholar
• Way JL. 1983. Cyanide antagonism. Fund Appl Toxicol 3:383–386.
   PubMedGoogle Scholar
• Way JL, Sylvester D, Morgan RL, Isom GE, Burrows GE, Tamulinas CB, Way, JL. 1984. Recent perspectives on the toxicodynamic basis of cyanide antagonism. Fund Appl Toxicol 4:231–239.
   PubMedGoogle Scholar
• Way JL, Leung P, Ray L, Saunder C. 1985. Erythrocyte encapsulated thiosulfate sulfurtransferase. Bibl Haematol 51:75–81.
   PubMedGoogle Scholar
• Way JL, Cannon EP, Leung P, Davis R, McGuinn DW, Yao C, Chiou C, Naqi A. 1991. Antagonism of cyanide intoxication with rhodanese encapsulated within resealed erythrocytes. Adv Biosci 81:207–211.
   Google Scholar
• Westley J. 1981. Thiosulfate: Cyanide sulfurtransferase (rhodanese). Meth Enzymol 77:285–291.
   PubMedGoogle Scholar
• Xia X, Hu Z, Gao J, Qin D, Durst HD, Yin R. 2002. Light scattering study of the self-association behavior of long-chain branched poly(2-ethyloxazoline) in solvents. Langmuir 18:8302–8308.
   Web of Science ®Google Scholar
• Yin R, Qin D, Tomalia DA, Kukowsky-Latallo J, Baker JR. 1997. From dendrimers to dendrigrafts. Synthesis, characterization and applications. Polym Mater Sci Eng 77:206–207.
   Google Scholar
• Yin R, Zhu Y, Tomalia DA. 1998. Architectural copolymers: Rod-shaped, cylindrical dendrimers. J Am Chem Soc 120:2678–2679.
   Web of Science ®Google Scholar