Hasil Pencarian  ::  Simpan CSV :: Kembali

Abstrak :
ABSTRAK
Latar Belakang: MTA bersifat biokompatibel dan dapat digunakan untuk perawatan kaping pulpa. Saat ini dikembangkan semen berbasis kalsium silikat sama seperti MTA dengan penambahan steroid, yaitu Odontocem. Tujuan:Membandingkan efek toksisitas odontocem dan MTA-Angelus terhadap viabilitas sel fibroblas. Metode:Sel fibroblast embrio ayam direndam dalam larutan odontocemdan dan MTA-Angeluspada 24 dan 72 jam. Viabilitas sel dihitung menggunakanMTT Assay. Hasil:Pada kelompok odontcemdan MTA-Angelus, terdapat perbedaan bermakna (p≤0,05 ) dibandingkan dengan kontrol. Pada paparan 24 jam, tidak terdapat perbedaan bermakna antara odontocem dengan MTA-Angelus. Kesimpulan:Odontocem dan dan MTA-Angelus menurunkan viabilitas sel pada 24 jam dan meningkatkan pada 72 jam.ABSTRACT
Background:MTA is proved tobe biocompatible and can be used for pulp capping treatment.Currently, calcium silicate based cement similar to MTA with steroid,called Odontocem has been developed.Objective:To compare effects of odontocem and MTA-Angelus toxicity towards fibroblast cells viability.Method:Fibroblast cells of chicken embryonic were immersed separately in odontocem and MTA-Angelus solution for 24 and 72 hours.Cells viability was analyzed with MTT Assay.Result:There was a significant difference (p>0.05) in Odontocem and MTA-Angelus group compared to control.At the24-hour immersion, there was nosignificant difference between odontocem and MTA-Angelus.Conclusion:Odontocem and MTA-Angelus decreased the viability of fibroblast at 24 hours and increased them at 72 hours.;Background:MTA is proved tobe biocompatible and can be used for pulp capping treatment.Currently, calcium silicate based cement similar to MTA with steroid,called Odontocem has been developed.Objective:To compare effects of odontocem and MTA-Angelus toxicity towards fibroblast cells viability.Method:Fibroblast cells of chicken embryonic were immersed separately in odontocem and MTA-Angelus solution for 24 and 72 hours.Cells viability was analyzed with MTT Assay.Result:There was a significant difference (p>0.05) in Odontocem and MTA-Angelus group compared to control.At the24-hour immersion, there was nosignificant difference between odontocem and MTA-Angelus.Conclusion:Odontocem and MTA-Angelus decreased the viability of fibroblast at 24 hours and increased them at 72 hours.;Background:MTA is proved tobe biocompatible and can be used for pulp capping treatment.Currently, calcium silicate based cement similar to MTA with steroid,called Odontocem has been developed.Objective:To compare effects of odontocem and MTA-Angelus toxicity towards fibroblast cells viability.Method:Fibroblast cells of chicken embryonic were immersed separately in odontocem and MTA-Angelus solution for 24 and 72 hours.Cells viability was analyzed with MTT Assay.Result:There was a significant difference (p>0.05) in Odontocem and MTA-Angelus group compared to control.At the24-hour immersion, there was nosignificant difference between odontocem and MTA-Angelus.Conclusion:Odontocem and MTA-Angelus decreased the viability of fibroblast at 24 hours and increased them at 72 hours.;Background:MTA is proved tobe biocompatible and can be used for pulp capping treatment.Currently, calcium silicate based cement similar to MTA with steroid,called Odontocem has been developed.Objective:To compare effects of odontocem and MTA-Angelus toxicity towards fibroblast cells viability.Method:Fibroblast cells of chicken embryonic were immersed separately in odontocem and MTA-Angelus solution for 24 and 72 hours.Cells viability was analyzed with MTT Assay.Result:There was a significant difference (p>0.05) in Odontocem and MTA-Angelus group compared to control.At the24-hour immersion, there was nosignificant difference between odontocem and MTA-Angelus.Conclusion:Odontocem and MTA-Angelus decreased the viability of fibroblast at 24 hours and increased them at 72 hours.

Abstrak :
Latar belakang: Tujuan dari perawatan pulpa gigi adalah terjadinya regenerasi. Sel punca mampu menghasilkan sekretom yang mengandung growth factor bila dibiakkan pada suatu medium. Hal ini membawa perubahan pada terapi berbasis sel menjadi terapi dengan menggunakan sekretom dari sel punca. Tujuan: Menganalisis potensi CMWJ terhadap proliferasi sel fibroblas dalam berbagai konsentrasi. Metode: Sel fibroblas setelah starvasi dibiakkan dalam CMWJ konsentrasi 12,5; 25 dan 50 . Setelah 2 hari sel fibroblas dihitung menggunakan alat hitung sel otomatis. Hasil: Terdapat perbedaan bermakna p le;0,05 jumlah sel pada kelompok 12,5 dan 50. Kesimpulan: konsentrasi 12,5 CMWJ memiliki potensi terbesar terhadap proliferasi sel fibroblas.

---

Background: The goal of dental pulp treatment is regeneration instead of repair. Stem cells from Wharton's Jelly umbilical cord can secrete growth factors in cultured medium. These secretome may open future therapeutic options for cell free based therapies. Objectives: This study was performed to evaluate potency of CMWJ in improving serum starved fibroblast. Methods: A quasi experimental design was done in serum starved fibroblasts. After cultured in 12.5 25 and 50 concentration of CMWJ for 48 hours, the proliferation was measured by using automatic cell count machine. Result: Cultivation of serum starved fibroblasts showed elevation of proliferation in 12,5 concentration of WJMSCs CM compared with 50 concentration, in significant result were shown p le 0,05.

Abstrak :
Latar Belakang: Temulawak (Curcuma xanthorrhiza Roxb.) adalah tanaman berkhasiat obat asli Indonesia dan merupakan tanaman obat unggulan untuk dikembangkan menjadi obat herbal terstandar. Pada beberapa penelitian, ekstrak etanol temulawak (EET) telah terbukti berkhasiat sebagai antimikroba, namun belum diketahui keamanannya terhadap jaringan mukosa mulut. Tujuan: Mengetahui sitotoksisitas ekstrak etanol temulawak (EET) terhadap sel fibroblas gingiva manusia (in vitro). Metoda: Model sel fibroblas gingiva diperoleh dari kultur primer jaringan gingiva manusia. Ekstrak etanol temulawak (1%, 2,5%, 5%, 10%, 20%, 40%) dipaparkan pada sel fibroblas gingiva dengan durasi paparan 1 jam, 3 jam, dan 24 jam. Viabilitas sel pasca paparan EET dianalisis dengan uji MTT (3-(4,5-dimethyl-thiazol-2-yl)-2,5-diphenyl-tetrazolium bromide) dan sitotoksisitas ditetapkan berdasarkan Inhibition Concentration 50% (IC50). Sedangkan, jumlah sel pasca paparan EET dievaluasi dengan metoda exclusion dye/trypan blue. Hasil: Model sel fibroblas gingiva dapat diperoleh dari kultur primer jaringan gingiva dan secara morfologi teridentifikasi sebagai sel fibroblas. Berdasarkan nilai IC50, EET pada konsentrasi >20% pasca paparan 1 dan 3 jam dan konsentrasi ≥10% pasca paparan 24 jam sitotoksik terhadap sel fibroblas gingiva. Jumlah sel fibroblas gingiva menurun sesuai dengan peningkatan konsentrasi pada durasi paparan 24 jam. Kesimpulan: Ekstrak etanol temulawak memiliki efek sitotoksik terhadap sel fibroblas gingiva. Sitotoksisitas ekstrak etanol temulawak dipengaruhi oleh konsentrasi dan durasi paparan. ......Background: Javanese turmeric (Curcuma xanthorrhiza Roxb.) is a herbal plant native to Indonesia and is a superior herbal plant to be developed into a standardized herbal medicine. In some studies, Curcuma xanthorrhiza ethanolic extract (CXEE) had been reported to have antimicrobial effect. However, its safety has not been evaluated for oral mucosal tissue. Objective: To evaluate the cytotoxicity of Curcuma xanthorrhiza ethanolic extract to human primary gingival fibroblast cells (in vitro). Method: Gingival fibroblast cells model were cultured from human primary gingival tissues. CXEE (1%, 2,5%, 5%, 10%, 20%, 40%) was added into gingival fibroblast culture for 1 h, 3 hrs, and 24 hrs. Cells viability after treatment of EET was analized with the 3-(4,5-dimethyl-thiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay and determined by Inhibition Concentration 50% (IC50). Meanwhile, cell density of treated cells was determined by exclusion dye/Trypan Blue. Result: Primary culture of human gingival tissue was able to produce gingival fibroblast cells model that was morphologically identified. Based on IC50, CXEE was cytotoxic againts gingival fibroblast cells at >20% of final concentration after 1 hr and 3 hrs treatment and at ≥10% of final concentration after 24 hrs treatment. Cell density of gingival fibroblast cells showed reduction as the increase of extract concentration in 24 hrs treatment. Conclusions: Curcuma xanthorrhiza ethanolic extract shows cytotoxic effect againts gingival fibroblast cells and is affected by concentration and duration of treatment.

Abstrak :
Latar Belakang: Obat antifungal sintetik dilaporkan menimbulkan reaksi gastrointestinal. Ekstrak etanol temulawak merupakan tanaman obat yang memiliki efikasi sebagai antijamur. Untuk dijadikan obat alternatif, ekstrak etanol temulawak harus biokompatibel terhadap sel inang. Tujuan: Menganalisis efek sitotoksitas ekstrak etanol temulawak terhadap sel fibroblast gingiva secara in vitro dengan live/dead staining. Metode: Sel fibroblast gingiva passage kedua dikultur sebanyak 1,4 x 104 sel/wells di atas cover glass dalam 12 wells plate. Sel diberi perlakuan dengan konsentrasi ekstrak etanol temulawak 5% dan 20% dengan waktu paparan 1 jam, 3 jam, dan 24 jam. Viabilitas dilihat dari uji live/dead staining menggunakan confocal laser scanning microscope dengan fluorescent dye SYTO9 ex/em max: 480/500nm, PI ex/em max: 490/635nm. Hasil: intensitas fluorescent semakin tinggi berbanding lurus dengan peningkatan konsentrasi ekstrak etanol temulawak. Kesimpulan: ekstrak etanol temulawak memiliki efek sitotoksik pada konsentrasi 5% dan 20% pada sel fibroblast gingiva. ......Background: Synthetic antifungal drugs are reported to cause gastrointestinal reactions. Ethanol turmeric extract is a herbal drug that has antifungal efficacy. To be used as an alternative drug, ethanol turmeric extract must be biocompatible with host cells. Objective: Analyze the cytotoxicity of ethanol turmeric extract on gingival fibroblasts in vitro with live/dead staining. Methods: The second passage gingival fibroblast cell was cultured as much as 1.4 x 104 cells / wells on the cover glass in 12 well plates. Cells were treated with ethanol turmeric extract concentrations of 5% and 20% with exposure time of 1 hour, 3 hours and 24 hours. Viability seen from live/dead staining assay using confocal laser scanning microscope with fluorescent dye SYTO9 ex/em max: 480/500nm, PI ex/em max: 490/635nm. Results: The higher fluorescent intensity is linear to increase in concentration of dilution ethanol turmeric extract. Conclusion: Ethanol turmeric extract has a cytotoxic effect at concentrations of 5% and 20% on gingival fibroblast cells.