Journals / Turkish Journal of Medical Sciences / 2018 / Cilt: 48 - Sayı: 6

The histopathological effects of calcium triglyceride bone cement and chitosan on the healing of experimental bone defects

Pages
1268–1277
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

After evaluating theresults, both materials were found not to be very useful in the bone healing process.Conclusion: CTBC remained for a long time without being resorbed; it can be used as a placeholder in large bone defects, whereas thegel form of chitosan cannot be utilized for this purpose because it was resorbed in the first 7 days.

📌 3 Key Takeaways

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Objective & Hypothesis:Background/aim: This study evaluated the histopathological effects of two different bone grafts, calcium triglyceride bone cement(CTBC) and chitosan, on the healing of experimental bone defects.Materials and methods: Ninety-two Sprague Dawley male rats, with a weight of 240 ± 20 g, were used.
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Key Findings & Data:Two experimental groups thatconsisted of 64 rats were divided into four subgroups due to the sacrification days, which were 7, 14, 30, and 60.
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Conclusion & Impact:After evaluating theresults, both materials were found not to be very useful in the bone healing process.Conclusion: CTBC remained for a long time without being resorbed; it can be used as a placeholder in large bone defects, whereas thegel form of chitosan cannot be utilized for this purpose because it was resorbed in the first 7 days.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Background/aim: This study evaluated the histopathological effects of two different bone grafts, calcium triglyceride bone cement(CTBC) and chitosan, on the healing of experimental bone defects.Materials and methods: Ninety-two Sprague Dawley male rats, with a weight of 240 ± 20 g, were used. Two experimental groups thatconsisted of 64 rats were divided into four subgroups due to the sacrification days, which were 7, 14, 30, and 60. After creating an 8-mmlong and 1-mm-wide cortico-cancellous bone defect in the right tibia of each rat, CTBC and chitosan were applied to the bone defects.In the main group, after creating the bone defects in the right tibias, we kept those empty to serve as the control group. We evaluatedinflammation, foreign body reaction, necrosis, fibrosis, new bone formation, and the residual graft material at 7, 14, 30, and 60 days.Results: In both the CTBC and chitosan groups, the new bone formation was higher than that in the control group, whereas foreign bodyreaction and residual graft material in the CTBC group and fibrosis in the chitosan group were significantly higher. After evaluating theresults, both materials were found not to be very useful in the bone healing process.Conclusion: CTBC remained for a long time without being resorbed; it can be used as a placeholder in large bone defects, whereas thegel form of chitosan cannot be utilized for this purpose because it was resorbed in the first 7 days.

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Cite This Article

ÇANKAYA, A. B., YILDIRIM, M. S., ATALAY, B., ORAL, C. K., USLUCAN, L. (2022). The histopathological effects of calcium triglyceride bone cement and chitosan on the healing of experimental bone defects. Turkish Journal of Medical Sciences, Cilt: 48 - Sayı: 6, 1268–1277. https://ajindex.com/articles/610346

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References (12)

  1. Rabie ABM, Lie KEN, Jie RKP. Integration of endochondral bone grafts in the presence of demineralized bone matrix. Int J Oral Maxillofac Surg 1996; 25: 311-318.
  2. Redondo LM, Cantera JMG, Hernândez AV, Puerta CV. Effect of particulate porous hydroxyapatite on osteoinduction of demineralized bone autografts in experimental reconstruction of the rat mandible. Int J Oral Maxillofac Surg 1995; 24: 445- 448. Aaboe M, Pinholt ME, Hjorting-Hansen E. Healing of experimentally created defects: a review. Br J Oral Maxillofac Surg 1995; 33: 312-318. Bernard GW. Healing and repair of osseous defects. Dent Clin North Am 1991; 35: 469-477. Parikh SN. Bone graft substitutes: past, present, future. J Postgrad Med 2002; 48: 142-148.
  3. Buttermann G, Glazer P, Bradford D. The use of bone allografts in the spine. Clin Orthop 1996; 324: 75-85.
  4. Greenwald AS, Boden SD, Goldberg VM, Khan Y, Laurencin CT, Rosier RN. Bone graft substitutes: facts, fictions, and applications. J Bone Joint Surg 2001; 83: 98-103.
  5. Szpalski M, Gunzburg R. Applications of calcium phosphatebased cancellous bone fillers in trauma surgery. Orthopaedics 2002; 25: 601-609.
  6. Kumar P, Vinitha B, Fathima G. Bone grafts in dentistry. J Pharm Bioall Sci 2013; 5: 125-127.
  7. Aichelmann-Reidy ME, Yukna RA. Bone replacement grafts. The bone substitutes. Dent Clin North Am 1998; 42: 491-503.
  8. Stevenson S, Emery SE, Goldberg VM. Factors affecting bone graft incorporation. Clin Orthop Relat Res 1996; 324: 66-74.
  9. Atay MH, Yılmaz FR. Investigation histopathologically of two different bone grafts. Dicle Tıp Dergisi 2005; 32: 172-178 (article in Turkish with a summary in English). Tomak Y, Dabak N, Kökçü C, Gülman B, Karaismailoğlu TN, Andaç A. Our clinical experience with the use of allografts and bone banking. Acta Orthopaedica et Traumatologica Turcica 2000; 34: 139-146 (article in Turkish with an abstract in English). Veth R, Schreuder B, Beem H, Pruszcynski M, Rooy J. Cryosurgery in aggressive, benign, and low-grade malignant bone tumours. Lancet Oncol 2005; 6: 25-34.
  10. Azad AK, Sermsintham N, Chandrkrachang S, Stevens WF. Chitosan membrane as a wound-healing dressing: characterization and clinical application. J Biomed Mater Res B Appl Biomater 2004; 69: 216-222.
  11. Klokkevold PR, Fukayama H, Sung EC, Bertolami CN. The effect of chitosan (poly-N-acetyl glucosamine) on lingual hemostasis in heparinized rabbits. J Oral Maxillofac Surg 1999; 57: 49-52.
  12. Liu H, Du Y, Wang X, Sun L. Chitosan kills bacteria through cell membrane damage. I