Fanny M Laihad
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Bioviabilitas Hidroksiapatit Ekstrak Cangkang Kerang Darah (Anadara granosa) Terhadap Sel Punca Mesenkimal Sebagai Bahan Graft Tulang Arlita Dewi Nastiti; Widyastuti; Fanny M Laihad
Denta Journal Kedokteran Gigi Vol 9 No 2 (2015): Agustus
Publisher : Fakultas Kedokteran Gigi Universitas Hang Tuah

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Abstract

Background: One of a bone defect fillers is ahydroxyapatite. Hydroxyapatite can be obtained from Anadara granosa shells extract that have high calcium content. The mineral content can be used as a bone filler material for bone grafting. However, the material is not known bioviability to against periodontal tissues so that was needed bioviability testing. This bioviability testing using mesenchymal stem cells as mesenchymal stem cells can differentiate into periodontal tissues. Purpose: To determine bioviability Anadara granosa shell extract on mesenchymal stem cells. Materials and Methods: This study was conducted using post-only control group design. Mesenchymal stem cells in 96 wells were divided into a control group of cells (n=7), media controls (n=7), and treatment (n=7). The treatment group were given various doses of the Anadara granosa shell extract with a concentration 54 mg/ml, 27 mg/ml, 13.5 mg /ml and 6.75 mg/ml. The mesenchymal stem cells were incubated for 24 hours before and after treatment. Once given MTT, the optical density is read by ELISA reader and calculated the percentage of viability. The cell viability data were analyzed with KruskalWallis statistical test, Mann-Whitney. Results: From the results showed that an increase in cell viability to Anadara granosa shell extract. Increased cell viability starting treatment group concentration of 54 mg/ml (23,,67%), 27 mg/ml (57,43%), 13,5 mg/ml (68,87%), 6,75 mg / ml (81,92%). The highest cell viability at concentrations of 6,75 mg/ml (81,92%). Conclusion: Bioviability extract blood clam Anadara granosa shell have the highestconcentration of 6,75 mg/ml and bioviabilitas lowest cell at a concentration of 54 mg/ml.
Pengaruh Induksi Aspergillus niger/brasiliensis Strain ATCC ® 16404™ Secara Sistemik dan Pencabutan Gigi Terhadap Jumlah Koloni pada Mukosa Gingiva Yanuardi Kristandia; Fanny M Laihad; Astrid Palmasari
Denta Journal Kedokteran Gigi Vol 9 No 2 (2015): Agustus
Publisher : Fakultas Kedokteran Gigi Universitas Hang Tuah

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30649/denta.v9i2.18

Abstract

Background: Prevention of gingival mucosal tissue damage caused by aspergillus niger the invasive fungal infection in the mouth is still difficult to determine its diagnosis and therapy. The cause of maxillary gingiva mucosal damage can be indicated as systemic fungal infections triggered by tooth extraction. There have been no research yet about the effect of invasive fungal aspergillus niger infections in the maxillary mucosa that has been performed tooth extraction and no tooth extraction. Purpose: To determine the effect of Aspergillus niger/brasiliensis strain ATCC ®16404 ™ induction systemically and tooth extraction action to the number of colonies on the maxillary gingiva mucosa. Materials and Methods: This study used post test only control group design. Thirty two adult male wistar rats were randomly divided into 4 groups: group K-, group P1 had tooth extraction, group P2 injected 0.3 ml by Aspergillus niger strain ATCC®16404 ™ 0.5 Mc Farland, P3 had extraction of maxillary tooth and injection 0.3 ml of the fungus aspergillus niger strain ATCC®16404 ™ 0.5 Mc Farland. Swabbing were applied on each group (day 1,3,5) in the maxillary mucosa and cultured on saboround dextrose agar (SDA) media with the spreader technique and incubated (37°C) for 48 hours Data were analyzed by Kruskal Wallis. Result: There is no significant difference in the amount of the fungus aspergillus niger in each group. Conclusion: Induction of aspergillus niger systemic wasn’t able to lead to significant conditions of the oral cavity, and therefore revocation isn’t a factor that that triggered the severity of the onset of aspergillus niger.