Updated on 19 July 2013
SMC Biotechnology is currently developing SMC-103 as a bone-healing device that can be delivered to the exact site of injury or damage to augment the body's natural healing process.
Singapore: SMC Biotechnology, a regenerative medicine company focused on developing carbohydrate compounds that enhance tissue regeneration, recently published data in the online journal Biomaterials, which suggests that its proprietary sugar compound SMC-103 greatly enhances bone repair.
Researchers found that affinity-selected heparan sulfate (HS) improved bone repair by increasing the bioavailability, bioactivity and half-life of the pro-healing compound, bone morphogenetic protein-2 (BMP-2). SMC-103 is a glycosaminoglycan (GAG), a naturally occurring substance composed of chains of paired sugar units. SMC Biotechnology is currently developing SMC-103 as a bone-healing device that can be delivered to the exact site of injury or damage to augment the body's natural healing process.
"This is the first time that an affinity-isolated sugar has been used to aid the body's natural repair processes," said Dr Simon Cool, co-founder, SMC Biotechnology, and the lead investigator of the study. "This could have strong implications in the clinic and shows that a sugar device can be used to promote bone healing rather than the use of a bone graft taken from the patients' hip bone or the application of extra BMP-2, both of which are associated with unwanted side-effects," Dr Cool said.
The study was conducted by researchers at the Glycotherapeutics Group, Institute of Medical Biology at the Agency for Science, Technology and Research (A*Star) in Singapore. To develop a specific GAG for bone repair, Dr Cool and Dr Victor Nurcombe, co-founder of SMC Biotechnology, and fellow researchers formulated a peptide-based affinity platform to isolate a unique BMP-2 binding HS variant from commercially available preparations of HS to ensure the translation into the clinic would be cost-effective.
Their theory was that the HS variant, once bound to BMP-2 produced by the body at the site of a bone injury, would prolong the growth factor's half-life and enhance its bioactivity. When the HS variant was delivered into critical-sized bone defects in preclinical studies, it enhanced bone healing at levels comparable to BMP-2 therapy alone. The study showed that BMP-2 binds to HS with a greater affinity than other sulfated GAGs, and that the unique characteristics of HS variants isolated based on growth factor affinity, validate this technology as a platform with high therapeutic utility.