Volume 100A, Issue 12 pp. 3267-3275

Evaluation of bone regeneration, angiogenesis, and hydroxyapatite conversion in critical-sized rat calvarial defects implanted with bioactive glass scaffolds

Lianxiang Bi

Lianxiang Bi

Department of Oral Biology, UMKC School of Dentistry, University of Missouri–Kansas City, Kansas City, Missouri 64108-2784

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Steve Jung

Steve Jung

Department of Materials Science and Engineering, Missouri University of Science and Technology, Rolla, Missouri 65409

Mo-Sci Corporation, Rolla, Missouri 65401

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Delbert Day

Delbert Day

Department of Materials Science and Engineering, Missouri University of Science and Technology, Rolla, Missouri 65409

Center for Bone and Tissue Repair and Regeneration, Missouri University of Science and Technology, Rolla, Missouri 65409

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Katie Neidig

Katie Neidig

Department of Oral Biology, UMKC School of Dentistry, University of Missouri–Kansas City, Kansas City, Missouri 64108-2784

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Vladimir Dusevich

Vladimir Dusevich

Department of Oral Biology, UMKC School of Dentistry, University of Missouri–Kansas City, Kansas City, Missouri 64108-2784

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David Eick

David Eick

Department of Oral Biology, UMKC School of Dentistry, University of Missouri–Kansas City, Kansas City, Missouri 64108-2784

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Lynda Bonewald

Corresponding Author

Lynda Bonewald

Department of Oral Biology, UMKC School of Dentistry, University of Missouri–Kansas City, Kansas City, Missouri 64108-2784

Department of Oral Biology, UMKC School of Dentistry, University of Missouri–Kansas City, Kansas City, Missouri 64108-2784Search for more papers by this author
First published: 26 June 2012
Citations: 109

How to cite this article: Bi L, Jung S, Day D, Neidig K, Dusevich V, Eick D, Bonewald L. 2012. Evaluation of bone regeneration, angiogenesis, and hydroxyapatite conversion in critical-sized rat calvarial defects implanted with bioactive glass scaffolds. J Biomed Mater Res Part A 2012:100A:3267–3275.

Abstract

Bioactive glasses are biocompatible materials that convert to hydroxyapatite in vivo, and potentially support bone formation, but have mainly been available in particulate and not scaffold form. In this study, borosilicate and borate bioactive glass scaffolds were evaluated in critical-sized rat calvarial defects. Twelve-week-old rats were implanted with 45S5 silicate glass particles and scaffolds of 1393 silicate, 1393B1 borosilicate, and 1393B3 borate glass. After 12 weeks, the defects were harvested, stained with hematoxylin and eosin to evaluate bone regeneration, Periodic Acid Schiff to quantitate blood vessel area, and von Kossa and backscatter SEM to estimate newly mineralized bone and hydroxyapatite conversion of bioactive glasses. The amount of new bone was 12.4% for 45S5, 8.5% for 1393, 9.7% for 1393B1, and 14.9% for 1393B3 (*p = 0.04; cf. 1393 and 1393B1). Blood vessel area was significantly higher (p = 0.009) with 45S5 (3.8%), with no differences among 1393 (2.0%), 1393B1 (2.4%), or 1393B3 (2.2%). Percent von Kossa-positive area was 18.7% for 45S5, 25.4% for 1393, 29.5% for 1393B1, and 30.1% for 1393B3, significantly higher (p = 0.014) in 1393B1 and 1393B3 glasses than in 45S5. 45S5 and 1393B3 converted completely to HA in vivo. The 1393B3 glass provided greater bone formation and may be more promising for bone defect repair due to its capacity to be molded into scaffolds. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A 100A:3267–3275, 2012.

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