## Abstract Systemic treatment with disodium ethaneβhydroxyβ1, 1βdiphosphonate is ineffective in inhibiting the calcergenic reactions induced in mouse skin by the lanthanides. In contrast, disodium dichloromethylene diphosphonate prevents lanthanide calcergy induced by 12 of the 15 compounds tested
Synthesis of osseous specific 32P-labeled disodium ethane-1-hydroxy-1,1-diphosphonate
β Scribed by Lionel D. McCreary; Andrew J. Tofe; Marion D. Francis
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- French
- Weight
- 337 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
β¦ Synopsis
High specific activity 32P-labeled disodium ethane-lhydroxy-1,l-diphosphonate has been prepared for specific use as a radiothera eutic ameliorative treatment of osseous tumors by reacting s2P-labeled phosphorus trichloride, acetic acid and water. This compound has been purified by crystallization of the disodium salt from a water-ethanol solution. Product identity and purity were established by reverse isotope dilution analysis. Spectrochemical quantitation, thin layer chromatography, radionuclide beta energy and half-life determinations are presented as essential procedures for establishing chemical and radiochemical purity when human distribution studies are planned.
π SIMILAR VOLUMES
Both disodium pyrophosphate and disodium ethane-hydroxy-1, 1-diphosphate inhibit the reaction of simple calcergy induced in the mouse by lead acetate. The pyrophosphate is effective only by a direct interaction with the lead salt and the disphosphonate is effective only before the occurrence of hist