The Effect of Poloxamer 407-Based Hydrogel on the Osteoinductivity of Demineralized Bone Matrix.
10.4055/cios.2014.6.4.455
- Author:
Jae Hyup LEE
1
;
Hae Ri BAEK
;
Kyung Mee LEE
;
Hyun Kyung LEE
;
Seung Bin IM
;
Yong Sung KIM
;
Ji Ho LEE
;
Bong Soon CHANG
;
Choon Ki LEE
Author Information
1. Department of Orthopedic Surgery, SMG-SNU Boramae Medical Center, Seoul National University College of Medicine, Seoul, Korea. spinelee@snu.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Demineralized bone matrix;
Osteoinductivity;
Carrier;
Poloxamer 407-based hydrogel
- MeSH:
Animals;
Bone Matrix/*physiology;
Cell Culture Techniques;
Decalcification Technique;
Excipients/*pharmacology;
Hydrogels/pharmacology;
Male;
Mesenchymal Stromal Cells/*drug effects;
Osteogenesis/*drug effects;
Poloxamer/*pharmacology;
Rats;
Rats, Nude
- From:Clinics in Orthopedic Surgery
2014;6(4):455-461
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: Demineralized bone matrix (DBM) is used for bone healing due to its osteoinductivity, but it requires a carrier for clinical application. Here, we report the effects on the osteoinductivity of DBM by use of a poloxamer 407-based hydrogel as the carrier, compared to sterile water. METHODS: DBM-W and DBM-H represent 27 wt% of DBM with sterile water and DBM with a poloxamer 407-based hydrogel, respectively. Both of the compositions were applied to human mesenchymal stem cell (MSC) cultures, and monitored for alkaline phosphatase (ALP) staining and ALP activity. Six 10-week-old athymic nude rats were used for abdominal muscle grafting with either DBM-W or DBM-H, and were tested by plane radiography, microfocus X-ray computed tomography (CT), and decalcified histology to evaluate ectopic bone formation. RESULTS: The DBM-W group showed stronger ALP staining at 7, 14, and 21 days of treatment, and significantly higher ALP activity at 7 and 14 days of treatment, compared to the DBM-H group. Plane radiography could not confirm the radio-opaque lesions in the rat ectopic bone formulation model. However, ectopic bone formation was observed in both groups by micro-CT. Compared to the DBM-H group, the DBM-W group showed higher bone volume, percent bone volume and trabecular number, and the difference in percent bone volume was statistically significant. Decalcified histology found bony tissue with lamellation in both groups. CONCLUSIONS: Our results suggest that poloxamer 407-based hydrogel has efficacy as a DBM carrier since it shows ectopic bone formation, but its effects on the quality and quantity of osteoblastic differentiation in rat abdominal ectopic bone and MSC are considered negative.
