Article
Development of Bioactive Sol-Gel Material Template for In Vitro and In Vivo Synthesis of Bone Material
Journal of Sol-Gel Science and Technology (impact factor:
1.63).
11/2000;
19(1):441-445.
DOI:10.1023/A:1008799513932
pp.441-445
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Citations (0)
- Cited In (4)
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Article: Macroscopical, histological, and morphometric studies of porous bone-replacement materials in minipigs 8 months after implantation.
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ABSTRACT: The aim of this investigation was to test the induction of bone formation and biodegradation of different biomaterials based on calcium phosphate (CaP). Up to now, hydroxyapatite and beta-tricalcium phosphate ceramics have routinely been sintered at temperatures of 1300 degrees C. The new CaP biomaterials tested are fabricated by a sol-gel process at only 700 degrees C. Critical-size defects (>5 cm(3)) in the mandible of 15 adult Goettingen minipigs were filled with 1 of the 2 new types of CaP biomaterials, or with 1 of 2 well-known old-type ceramics, or with a gelatin sponge (in the control group). Macroscopical, histological, and morphometric examination of the former defect areas were made 8 months postoperatively. Eight months after implantation of the new CaP biomaterials, complete bone formation was observed in the defect area, and at the same time, the foreign material was resorbed almost completely. After implantation of the classical types of ceramics, only incomplete bone formation and a lesser resorption rate of the foreign bodies were noted. The difference in the bone formation rate was significant: more than 93% for the new CaP biomaterials versus less than 58% for the classical types of ceramics (P < 0.01). The biological behavior of the new CaP biomaterials was better than that of the old-type sintered ceramic bone-grafting materials. These new CaP matrices are suitable for filling bone defects and are of interest for dentists, including implantologists, craniomaxillofacial and orthopedic surgeons, as well as traumatologists.Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics 12/2006; 102(5):606-13. · 1.50 Impact Factor -
Article: Neuartiges Knochenaufbaumaterial auf Kalziumphosphatbasis
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ABSTRACT: HintergrundAlle bisher angebotenen synthetischen Knochenersatzmaterialien auf Hydroxylapatit(HA)- und -Trikalziumphosphat(TCP)-Basis werden im Sinterverfahren bei Temperaturen von 1100–1500C produziert. 2 innovativ im Sol-Gel-Verfahren bei 200C hergestellte Knochenaufbaumaterialien auf Kalziumphosphatbasis mit Siliziumoxid (SiO2) weisen aufgrund des Herstellungsunterschieds neuartige Materialeigenschaften auf und wurden als Adjuvans im Langzeittierversuch getestet. Es sollte geklrt werden, in welchem Umfang diese im Niedertemperaturbereich hergestellten Knochenaufbaumaterialien die Osteogenese in Critical-size-Defekten stimulieren und welches Resorptionsverhalten sie aufweisen.Material und MethodeBei 18 adulten Gttinger Minischweinen wurden im Bereich der anterioren Mandibula perforierende Critical-size-Defekte (>5cm3) gesetzt. In Gruppe I (n=6) wurden diese mit einer biphasischen (60% HA und 40% TCP), in Gruppe II (n=6) mit einer monophasischen Variante (100% HA) des neuartigen Knochenaufbaumaterials aufgefllt. Gruppe III (n=6) bildete die Leerkontrolle. Nach 8Monaten wurde die Defektregion klinisch und histologisch/morphometrisch untersucht. Die statistische Evaluation erfolgte mittels Varianzanalyse fr Mehrfachvergleiche.ErgebnisseIn beiden Versuchsgruppen waren klinisch eine vollstndige Reossifikation der Defekte sowie ein hoher Biodegradationsgrad der Testmaterialien zu beobachten. In Gruppe II (reines HA) waren nach 8Monaten 98,7% des Biomaterials resorbiert. Dieser Wert lag in Gruppe I (HA und TCP) mit 93,7% etwas niedriger, wobei die Gruppendifferenz statistisch nicht signifikant war (p=0,483). Beide Knochenaufbaumaterialien stimulieren die Knochenneubildung deutlich. Die Defekte waren nach 8Monaten zu mehr als 93% mit Knochen aufgefllt. In der Kontrollgruppe lag die kncherne Durchbaurate der Defekte bei 48,4%. Dieser Unterschied war statistisch hoch signifikant (p<0,001).SchlussfolgerungIm Sol-Gel-Verfahren bei 200C hergestellte Knochenaufbaumaterialien auf Kalziumphosphatbasis weisen in vivo neben einer sehr guten Osteokonduktivitt ein verbessertes Resorptionsverhalten gegenber herkmmlichen Biokeramiken auf. Sie erscheinen daher fr die Therapie kncherner Defekte beim Menschen geeignet.BackgroundUp to now hydroxyapatite (HA) and -tricalciumphosphate (-TCP) ceramics have been routinely sintered at temperatures between 1100 and 1500C. Our new calcium ceramic is fabricated by a sol-gel process at 200C. The aim of this investigation was to test the biodegradation of and the induction of bone formation by this material.Material and methodsEighteen 1-year-old Goettingen minipigs were divided into three groups. Critical size defects (>5cm3) in the mandible were treated differently in all three animals (group 1: filling with 40% -TCP plus 60% HA, group 2: pure HA was applied, group 3 served as controls: only gelatinous material was given). Macroscopic and microscopic investigations of the former defects were made 8months postoperatively.ResultsIn groups 1 and 2 biodegradation of more than 93% of the new calcium phosphate formula was found 8months postoperatively and considered to be very good. No difference was observed between pure HA (group 2) and the combination of HA and -TCP (group 1). In both groups complete bone formation was seen macroscopically in the former defects. In the control group only incomplete bone formation with 48.4% of the defect area was noted. This difference was significant (p<0.001).DiscussionThe new calcium phosphate formula made by a sol-gel method at 120C seems to be suitable for filling bone defects and is of interest for orthopedic surgery, traumatology, craniomaxillofacial surgery, and dentistry.Mund- Kiefer- und Gesichtschirurgie 04/2012; 8(5):277-281. -
Article: Histological and histomorphometrical analysis of a silica matrix embedded nanocrystalline hydroxyapatite bone substitute using the subcutaneous implantation model in Wistar rats
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ABSTRACT: The clinical suitability of a bone substitute material is determined by the ability to induce a tissue reaction specific to its composition. The aim of this in vivo study was to analyze the tissue reaction to a silica matrix-embedded, nanocrystalline hydroxyapatite bone substitute. The subcutaneous implantation model in Wistar rats was chosen to assess the effect of silica degradation on the vascularization of the biomaterial and its biodegradation within a time period of 6 months. Already at day 10 after implantation, histomorphometrical analysis showed that the vascularization of the implantation bed reached its peak value compared to all other time points. Both vessel density and vascularization significantly decreased until day 90 after implantation. In this time period, the bone substitute underwent a significant degradation initiated by TRAP-positive and TRAP-negative multinucleated giant cells together with macrophages and lymphocytes. Although no specific tissue reaction could be related to the described silica degradation, the biomaterial was close to being fully degraded without a severe inflammatory response. These characteristics are advantageous for bone regeneration and remodeling processes.Biomedical Materials 05/2010; 5(3):035005. · 2.16 Impact Factor
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Keywords
Animal tests
biodegradable
biodegradation properties.Nanoporous silica gel
bone ingrowth.An
bone tissue
crystallinity
first steps
inoculated
low degree
microns
millimetres
new bone tissue
novel porous material
pores
temperatures
tissue culture medium
vitro formation