Bone Affinity of a Bisphosphonate-Conjugated Protein in Vivo

• Published in: Biotechnology progress 2000-12, Vol.16 (6), p.1115-1118
• Main Authors: Uludag, Hasan, Gao, Tiejun, Wohl, Gregory R., Kantoci, Darko, Zernicke, Ronald F.
• Format: Article
• Language: English
• Subjects: 1-amino-1,1-diphosphonate methane; Animals; Biological and medical sciences; Biotechnology; bisphosphonates; Bone and Bones - metabolism; Diphosphonates - metabolism; Disease Models, Animal; Female; Fundamental and applied biological sciences. Psychology; Health. Pharmaceutical industry; Industrial applications and implications. Economical aspects; Miscellaneous; Osteoporosis - metabolism; Ovariectomy; Rats; Rats, Sprague-Dawley; Serum Albumin, Bovine - metabolism
• ISSN: 8756-7938; 1520-6033
• DOI: 10.1021/bp000066y

Growth factors capable of stimulating bone formation are potential therapeutic agents for osteoporosis treatment. It is essential, however, that a targeting mechanism is incorporated into the growth factors to deposit them at osseous tissue with minimal distribution to extraskeletal sites. To this end, a strategy has been developed in which a bone‐seeking molecule, 1‐amino‐1,1‐diphosphonate methane (aminoBP), was chemically conjugated to a model protein, bovine serum albumin (BSA). This study was carried out to assess the bone affinity of the conjugates in a tibia injection model. Using ovariectomized (OVX) rats, initial (3 h) retention of BSA and aminoBP‐BSA were found to be equivalent when injected into the medullary cavity of tibia. After 1 day, an 8‐ and 12‐fold higher tibiae retention of the protein was obtained in normal and OVX rats as a result of aminoBP conjugation. A similar result (∼12‐fold difference) was also obtained in OVX rats after 3 days. We concluded that aminoBP conjugation to BSA imparted a high bone affinity and enhanced bone retention of proteins in normal and OVX rats.