4.8 Article

Bioabsorbable bone plates enabled with local, sustained delivery of alendronate for bone regeneration

期刊

JOURNAL OF CONTROLLED RELEASE
卷 222, 期 -, 页码 97-106

出版社

ELSEVIER
DOI: 10.1016/j.jconrel.2015.12.007

关键词

Alendronate; Bioabsorbable bone plate; Bone regeneration; Drug delivery

资金

  1. KRIBB [KGM4891511]
  2. Ministry of Health AMP
  3. Welfare, Republic of Korea [HI14C2310]
  4. Korea Health Technology RAMP
  5. D Project through the Korea Health Industry Development Institute (KHIDI) - Ministry of Health AMP
  6. Welfare, Republic of Korea [HI14C2194]
  7. Advanced medical new material (fiber) development program through the Ministry of Trade, Industry and Energy (MOTIE)
  8. Korea Institute for Advancement of Technology (KIAT) [R00001408]
  9. Korea Health Promotion Institute [HI14C0042020016] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

We prepared a bone plate enabled with the local, sustained release of alendronate, which is a drug known to inhibit osteoclast-mediated bone resorption and also expedite the bone-remodeling activity of osteoblasts. For this, we coated a bone plate already in clinical use (PLT-1031, Inion, Finland) with a blend of alendronate and a biocompatible polymer, azidobenzoic acid-modified chitosan (i.e., Az-CH) photo-crosslinked by UV irradiation. As we performed the in vitro drug release study, the drug was released from the coating at an average rate of 4.03 mu g/day for 63 days in a sustained manner. To examine the effect on bone regeneration, the plate was fixed on an 8 mm cranial critical size defect in living rats and the newly formed bone volume was quantitatively evaluated by micro-computed tomography (micro-CT) at scheduled times over 8 weeks. At week 8, the group implanted with the plate enabled with sustained delivery of alendronate showed a significantly higher volume of newly formed bone (52.78 +/- 6.84%) than the groups implanted with the plates without drug (23.6 +/- 3.81%) (p < 0.05). The plate enabled with alendronate delivery also exhibited good biocompatibility on H&E staining, which was comparable to the Inion plate already in clinical use. Therefore, we suggest that a bone plate enabled with local, sustained delivery of alendronate can be a promising system with the combined functionality of bone fixation and its expedited repair. (C) 2015 Elsevier B.V. All rights reserved.

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