Na3[B20H17NH3]: Synthesis and Liposomal Delivery to Murine Tumors

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 91; no. 8; pp. 3029 - 3033
• Main Authors: FEAKES, D. A, SHELLY, K, KNOBLER, C. B, HAWTHORNE, M. F
• Format: Journal Article
• Language: English
• Published: Washington, DC National Academy of Sciences of the United States of America 12.04.1994; National Acad Sciences
• Subjects: Animals; Atoms; Biological and medical sciences; Blood; Body weight; Boranes; Boranes - administration & dosage; Boranes - pharmacokinetics; Boron; Boron Neutron Capture Therapy - methods; Female; Isomers; Liposomes; Medical sciences; Mice; Mice, Inbred BALB C; Neoplasms, Experimental - metabolism; Oxidation-Reduction; Radiation therapy and radiosensitizing agent; Sodium; Tissue Distribution; Treatment with physical agents; Treatment. General aspects; Tumors; Encapsulation; Cage compound; Intravenous administration; Rodentia; Liposome; Neutron capture; Malignant tumor; Neutron therapy; Radiotherapy; Sodium Compounds; Vertebrata; Mammalia; Treatment; Mouse; Animal; Distribution; Dosage form; Pharmacokinetics; Chemical synthesis; Boron Compounds
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.91.8.3029

The polyhedral borane ion [n-B20H18]2-reacts with liquid ammonia in the presence of a suitable base to produce an apical-equatorial (ae) isomer of the [B20H17NH3]3-ion, [1-(2'-B10H9)-2-NH3B10H8]3-. The structure of this product has been confirmed by11B NMR spectroscopy and x-ray crystallography. This species undergoes acid-catalyzed rear-rangement to an apical-apical (a2) isomer, [1-(1'-B10H9)-2-NH3B10H8]3-, whose structure has been determined by11B NMR spectroscopy. The sodium salts of both the ae and the a2isomers of [B20H17NH3]3-have been encapsulated within small unilamellar liposomes, composed of distearoyl phosphatidylcholine/cholesterol (1:1), and investigated as boron-delivery agents for boron neutron capture therapy (BNCT) of cancer. The biodistribution of boron was determined after the injection of liposomal suspensions into BALB/c mice bearing EMT6 tumors. Both [B20H17NH3]3-isomers exhibited excellent tumor uptake and selectivity at very low injected doses, achieving peak tumor boron concentrations of 30-40 μ g of B/g of tissue and tumor/blood boron ratios of ≈5. The enhanced retention of the [B20H17NH3]3-isomers by EMT6 tumors may be attributed to their facile intracellular oxidation to an extremely reactive NH3-substituted [n-B20H18]2-ion, the electrophilic [B20H17NH3]-ion. Both isomers of [B20H17NH3]3-are at least 0.5 V more easily oxidized than other previously investigated species containing 20 boron atoms. In another experiment, [ae-B20H17NH3]3-was encapsulated in liposomes prepared with 5% PEG-2000-distearoyl phosphatidylethanolamine in the liposome membrane. As expected, these liposomes exhibited a longer circulation lifetime in the biodistribution experiment, resulting in the continued accumulation of boron in the tumor over the entire 48-hr experiment and reaching a maximum of 47 μ g of B/g of tumor.