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"Penelitian ini bertujuan untuk mengetahui viabilitas sel punca sum-sum tulang manusia setelah dipapar larutan ekstrak scaffold HA/alginat (30/70) atau scaffold HA/alginat/kitosan (30/50/20) selama 24, 48, atau 72 jam. Larutan ekstrak scaffold diuji dengan MTT. Hasil viabilitas sel pada pemaparan 24, 48, atau 72 jam scaffold HA/alginat secara berurutan 78,3±7,90%, 69,4±10,63%, 80,6±10,89%, sedangkan pada scaffold HA/alginat/kitosan secara berurutan 94,2±10,55%, 81,8±13,91%, 96,7±16,28%. Pada waktu pemaparan 24 jam, viabilitas sel antara scaffold HA/alginat dan scaffold HA/alginat/kitosan berbeda bermakna (p<0,05). Viabilitas sel scaffold HA/alginat/kitosan secara signifikan lebih tinggi dibandingkan dengan viabilitas sel scaffold HA/alginat pada waktu pemaparan 24 jam.

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This study aims to determine the viability of human bone marrow stem cells after exposed to the extract solution of HA/alginate (30/70) or HA/alginate/chitosan (30/50/20) scaffolds. The cell viability was evaluated by MTT assay. The cell viability of HA/alginate scaffold on 24, 48, or 72 hour is 78.3±7.90%, 69.4±10.63%, and 80.6±10.89%, respectively, while the cell viability of HA/alginate/chitosan scaffold is 94.2±10.55%, 81.8±13.91%, and 96.7±16.28%, respectively. The cell viability obtained from the HA/alginate and HA/alginate/chitosan scaffold in 24 hour is significantly different (p<0.05). The cell viability of HA/alginate/chitosan scaffold is significantly higher than that of the HA/alginate scaffold in 24 hour."

"[ABSTRAKMultifungsi untuk terapi kanker tulang dan regenerasi jaringan tulang mulai dipelajari dengan menggunakan scaffold komposit biopolimer dan magnetik. Penelitian ini bertujuan menyintesis dan mengarakterisasi scaffold karbonat apatit/kitosan/alginat/partikel magnetik kalsium alumina ferrit serta menganalisis viabilitas selnya. Pertama disintesis karbonat apatit kemudian dicampurkan dengan kitosan, alginat dan kalsium alumina ferrit kemudian di freeze drying untuk mendapatkan scaffold. Hasil menunjukkan terbentuknya struktur komposit. Kalsium alumina ferrit berbentuk irregular dan berukuran 0,5-2 μm. Magnetisasi partikel kalsium alumina ferrit dan scaffold magnetik ditunjukkan dengan magnetisasi saturasi, medan koersivitas dan magnetisasi remanen. Scaffold tersebut teramati tidak mempengaruhi viabilitas sel HaCaT.

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ABSTRACTMultifunction for bone cancer therapy and bone tissue regeneration has been studied using biopolymers and magnetic composite scaffolds. The aim of stud was to synthesize and characterize the carbonate apatite/chitosan/alginate/calcium aluminate ferrite composite scaffold as well as to analyze the cell viability. Firstly, carbonate apatite was synthesized and then was mixed with chitosan, alginate and calcium aluminate ferrite. Then the resulted gel was freeze dried to obtain thescaffold. Results indicated the formation of a composite structure. Calcium aluminate ferrite particle were irregular in shape and 0.5-2 μm in size. Magnetizations of the calcium aluminate ferrite particle and the magnetic scaffolds were demonstrated in the saturation magnetization, coercivity field and remanent magnetization. The produced scaffold was observed did not affect the viability of HaCaT cells., Multifunction for bone cancer therapy and bone tissue regeneration has been studied using biopolymers and magnetic composite scaffolds. The aim of stud was to synthesize and characterize the carbonate apatite/chitosan/alginate/calcium aluminate ferrite composite scaffold as well as to analyze the cell viability. Firstly, carbonate apatite was synthesized and then was mixed with chitosan, alginate and calcium aluminate ferrite. Then the resulted gel was freeze dried to obtain thescaffold. Results indicated the formation of a composite structure. Calcium aluminate ferrite particle were irregular in shape and 0.5-2 μm in size. Magnetizations of the calcium aluminate ferrite particle and the magnetic scaffolds were demonstrated in the saturation magnetization, coercivity field and remanent magnetization. The produced scaffold was observed did not affect the viability of HaCaT cells.]"

"Latar Belakang: Perawatan pulpa vital adalah perawatan konservatif yang bertujuan menjaga pulpa tetap sehat pada gigi yang mengalami trauma, karies, prosedur restorasi dan kelainan anatomi. Mineral Trioxide Aggregate (MTA) merupakan bahan bioaktif yang sering digunakan perawatan pulpa vital. Pengembangan MTA dilakukan untuk meningkatkan karakter fisik dan biokompatibilitasnya. Tujuan: Mengetahui pengaruh aplikasi material MTA dan MTA modifikasi carboxymethyl chitosan (CMC) terhadap viabilitas sel fibroblas. Metode: Sel fibroblas yang telah mengalami serum starvation selama 24 jam, diaplikasikan media kultur berupa material bioaktif yang berbeda yaitu MTA, MTA modifikasi CMC 5% dan 10 % serta DMEM sebagai kontrol. Pengaruh viabilitas sel fibroblas 24 dan 72 jam dinilai dan dihitung menggunakan MTT Assay. Analisis data menggunakan uji statistik One-Way ANOVA, dilanjutkan Post Hoc Bonferonni. Hasil: Terdapat perbedaan bermakna viablitas sel fibroblas pada kelompok MTA, MTA-CMC 5% dan 10% pada periode waktu pengamatan 24 dan 72 jam. Nilai viabilitas terendah terdapat pada kelompok MTA 72 jam sedangkan nilai viabilitas tertinggi terdapat pada kelompok MTA-CMC 5% 24 jam. Kesimpulan: MTA, MTA modifikasi CMC 5% dan 10% memengaruhi viabilitas sel fibroblas pada periode pengamatan 24 dan 72 jam. MTA modifikasi CMC 5% pengamatan 24 jam menghasilkan nilai viabilitas tertinggi dan termasuk kategori material yang tidak toksik.

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Background: Vital pulp treatment is a conservative treatment designed to keep the pulp healthy in teeth that have experienced trauma, caries, restoration procedures and anatomical abnormalities. Mineral Trioxide Aggregate (MTA) is one of the bioactive materials that is often used for vital pulp treatment. The development of MTA was carried out to improve its physical characteristics and biocompatibility.Objective: To determine the effect of the application of MTA modified carboxymethyl chitosan (CMC) and MTA materials on the viability of fibroblast cells.Methods: Fibroblast cells that had undergone 24 hours serum starvation were cultured in the different media in in every group MTA and MTA modified CMC concentrations of 5% and 10% and DMEM as a control. The effect of fibroblast cell viability at 24 hours and 72 hours was assessed based on the percentage of live cells calculated using the MTT Assay. Then the results obtained were analyzed using the SPSS statistical test. The distribution of the data was normal so that the One-Way ANOVA parametric test was carried out, followed by Post Hoc Bonferonni.Results: MTT Assay test, it was found that there was a significant difference in the viability of fibroblast cells in the MTA, MTA-CMC groups of 5% and 10% in the 24 and 72 hours observation periods. The lowest viability value was found in the MTA group with 72 hours of observation, while the highest viability value was found in the 5% MTA-CMC group with 24-hour observation. Conclusion: MTA, MTA modified CMC 5% and 10% affected the viability of fibroblast cells in the 24-hour and 72-hour observation periods. MTA modified CMC 5% at 24-hour observation resulted in the highest viability value and included in the category of non-toxic material."

"Ekstrak mangostin sebagai biomaterial baru yang ditambahkan pada scaffold karbonat apatit / alginat / kitosan diharapkan dapat membunuh sisa sel kanker pada tulang setelah dilakukan tindakan pembedahan. Semua material yang akan digunakan pada tubuh harus memenuhi syarat untuk dapat diterima jaringan dan tidak menimbulkan reaksi toksik pada tubuh. Tujuan penelitian ini untuk memperoleh informasi mengenai viabilitas sel terhadap scaffold komposit karbonat apatit / alginat / kitosan dengan ekstrak mangostin. Scaffold dibuat dari bahan serbuk karbonat apatit / alginat / kitosan dengan ekstrak mangostin menggunakan metode freeze drying. Karakterisasi dilakukan dengan XRD, FTIR, SEM dan dilanjutkan dengan viabilitas sel menggunakan MTT assay pada konsentrasi 10%, 7.5%, 5%, 2.5%, 1% atau 0.5%. Hasil penelitian diperoleh porositas scaffold komposit karbonat apatit / alginat / kitosan dengan ekstrak mangostin berkisar 50 ? 300 μm. Diperoleh viabilitas tertinggi dari scaffold komposit karbonat apatit / alginat / kitosan dengan ekstrak mangostin pada konsentrasi 0.5 %. Terdapat perbedaan bermakna antara viabilitas sel dari sampel scaffold karbonat apatit / alginat / kitosan dibandingkan terhadap viabilitas sel dari sampel scaffold karbonat apatit / alginat / kitosan dengan ekstrak mangostin pada konsentrasi 10 % dan 7.5 % (P<0.05) tetapi tidak memberikan perbedaan bemakna pada konsentrasi 5%, 2.5%, 1% dan 0.5% (P>0.05). Dapat disimpulkan scaffold komposit karbonat apatit / alginat / kitosan dengan ekstrak mangostin mempengaruhi viabilitas sel sehingga bersifat sitotoksik.

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Mangosteen Extract as a new biomaterial to be added to carbonate apatite scaffold / alginate / chitosan is expected to remove any remaining cancer cells in the bones after surgery. All materials which will used on the body must eligible to be accepted by system and does not cause toxic reactions in the body. The purpose of this study was obtaining information on cell viability against carbonate apatite composite scaffold / alginate / chitosan with mangosteen extract. The scaffold is made of carbonate apatite powder / alginate / chitosan with extract mangosteen using freeze drying method. Characterization are performed by XRD, FTIR, SEM and followed by cell viability using MTT assay at concentrations of 10%, 7.5%, 5%, 2.5%, 1% or 0.5%. The results were obtained composite scaffold porosity carbonate apatite / alginate / chitosan mangosteen extract range 50-300 lm. Obtained the highest viability of carbonate apatite composite scaffold / alginate / chitosan with mangosteen extract at a concentration of 0.5%. There is a significant difference between the cells viability of composite of scaffold carbonate apatite / alginate / chitosan samples compared to the cells viability of composite of scaffold carbonate apatite / alginate / chitosan with mangostin extract samples at concentrations of 10% and 7.5% (p<0.05), but no difference significant in the concentration 5%, 2.5%, 1% and 0.5% (p>0:05). It can be concluded composite of scaffold carbonate apatite / alginate / chitosan with mangostin extract affect the viability of cells that are cytotoxic."

"ABSTRAKLatar belakang: Virgin Coconut Oil VCO memiliki efek antibakteri. Tujuan: Menganalisis efek pemberian VCO berbagai konsentrasi terhadap viabilitas bakteri Actinomyces sp dan Prevotella sp. Metode penelitian: Bakteri Actinomyces sp dan Prevotella sp dipaparkan dengan VCO konsentrasi 12,5 , 25 , 50 , dan 100 . Selanjutnya dilakukan uji viabilitas dengan MTT Assay. Hasil: Penurunan viabilitas Actinomyces sp bermakna pada pemberian VCO 25 dan penurunan viabilitas Prevotella sp bermakna pada pemberian VCO 100 . Kesimpulan: Pada pemberian VCO dengan berbagai konsentrasi, penurunan viabilitas bakteri Actinomyces sp lebih besar dibandingkan dengan Prevotella sp.

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ABSTRACT Background Virgin Coconut Oil VCO has antibacterial effect. Objective To analyze effects of VCO administered in various concentrations on viability of Actinomyces sp and Prevotella sp. Methods Actinomyces sp and Prevotella sp was exposed to VCO in concentrations 12.5 , 25 , 50 and 100 . Afterwards, viability testing with MTT Assay was conducted. Results Significantly reduce viability was reached by Actinomyces sp with VCO 25 and significance was reached by Prevotella sp administering VCO 100 . Conclusion When VCO was administered in various concentrations, the decline rate in bacterial viability of Actinomyces sp was higher than Prevotella sp. "

"Tulang merupakan salah satu penyusun sistem gerak manusia yang rentan mengalami kerusakan berupa fraktur akibat kecelakaan atau osteoporosis. Mekanisme remodeling tulang dapat membantu memperbaiki struktur tulang, namun bergantung pada kerusakannya. Rekayasa jaringan tulang, perancah, merupakan salah satu penyembuhan yang dapat digunakan untuk membantu regenerasi jaringan tulang. Perancah harus memiliki biokompatibilitas serta osteokonduktivitas yang baik. Biokeramik seperti hidroksiapatit (HAp) dan biphasic calcium phosphate (BCP) digunakan sebagai perancah karena strukturnya yang mirip tulang asli. Temulawak, Curcuma xanthorrhiza (CuX) merupakan tanaman obat yang dapat digunakan untuk meningkatkan sifat antiinflamasi pada perancah. Pada penelitian ini, kitosan (CS), hyaluronic acid (HA), dan ekstrak temulawak (CuX) digunakan sebagai material utama perancah dengan HAp dan BCP sebagai variasinya. Ekstraksi temulawak dilakukan dengan metode Soxhlet dan ekstraksi HAp dan BCP dilakukan dengan metode kalsinasi tulang ikan tuna pada suhu 600 °C dan 1000 °C. Ketiga perancah difabrikasi dengan metode freeze drying dan dikarakterisasi dengan uji viabilitas dan proliferasi sel. HAp dan BCP sebagai variabel bebas menghasilkan viabilitas sel yang lebih baik dibandingkan dengan perancah kontrol pada uji direct selama 4 hari. Namun, tingginya degradasi dari perancah mengakibatkan jumlah sel berkurang drastis dari pertama kali ditanam. Pada uji viabilitas indirect menggunakan MTT assay, HAp pada perancah mendukung viabilitas sel secara signifikan dibandingkan dengan BCP dan kontrol. Secara keseluruhan, ketiga variasi perancah berhasil menyediakan tempat bagi sel untuk hidup dan tidak beracun.

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Bones are one of the musculoskeletal systems in humans which vulnerable to damage as fractures because of accidents or osteoporosis. The remodeling mechanism in bone may help to fix the bone structure, but it depends on the extent of the damage. Bone tissue engineering as a scaffold is one of the methods to help bone regeneration. Bone tissue engineering as a scaffold is one of the methods to help bone regeneration. Scaffold must have good biocompatibility and osteoconductivity. Bioceramics such as hydroxyapatite (HAp) and biphasic calcium phosphate are often used as scaffolds because their structure is similar to natural bone. Temulawak, or Curcuma xanthorrhiza (CuX), is a herbal plant that improves anti-inflammation. This study uses chitosan (CS), hyaluronic acid (HA), and temulawak extract (CuX) as the primary materials. This study uses extraction of temulawak using the Soxhlet method and extraction of HAp and BCP using calcination at 600 °C and 1000 °C. Scaffolds with the combination of CS/HA/CuX, CS/HA/CuX/HAp, and CS/HA/CuX/BCP fabricated using the freeze-drying method and characterized with proliferation and viability test. The HAp dan BCP as dependent variables generated better ability in the viability test than CS/HA/CuX scaffold on the direct test for four days. However, the high degradation from the sample yielded to loss of cells. For indirect tests using MTT assay, the addition of HAp in the scaffold showed better performance in the cell viability significantly more than BCP and control scaffolds. Overall, all scaffolds provided good places for the cell to live and showed non-toxic behavior towards the cells."

"Pendahuluan: Breket Stainless Steel 17-4 PH merupakan salah satu breket yang paling banyak digunakan dalam bidang Ortodonti dengan jangka waktu yang lama didalam rongga mulut, Penggunaannya yang lama mengakibatkan kerugian bagi kesehatan pengguna karena lepasnya ion nikel dan kromium akibat proses korosi. Oleh karena itu, tujuan dari penelitian ini adalah untuk mengatahui sitotoksisitas breket pada sel gingiva akibat lepasnya ion nikel dan kromium pada saliva buatan. Metode: Penelitian In Vitro dengan 2 kelompok breket Stainless Steel 17-4 PH lokal dan impor yang masing-masing berjumlah 24 buah breket. Tiap kelompok jumlah sampel dibagi tiga berdasarkan lama waktu perendaman breket di dalam saliva buatan selama 16, 28, dan 35 hari. Lepasan ion Cr dan Ni dalam saliva hasil perendaman breket di paparkan ke sel gingiva untuk di lakukan uji sitotoksisitas menggunakan MTT Assay. Terlihat seberapa besar viabilitas sel yang menandakan toksisitas breket. Hasil: Terdapat pola viabilitas sel yang berbeda antara breket Stainless Steel 17-4 PH lokal dan impor, namun secara statistik perbedaan viabilitas sel tersebut tidak signifikan, sehingga tidak terdapat perbedaan sitotoksisitas breket Stainless Steel 17-4 PH lokal dan impor. Kesimpulan: Uji sitotoksisitas pada braket Stainless Steel 17-4 PH lokal memperlihatkan pola viabilitas sel pada perendaman 16 hari lebih tinggi lalu ketika perendaman 28 hari tampak viabilitas sel menurun dan meningkat kembali pada perendaman 35 hari sedangkan uji sitotoksisitas pada braket Stainless Steel 17-4 PH impor memperlihatkan pola viabilitas sel pada perendaman 16 hari lebih rendah bila dibandingkan dengan perendaman 28 hari dan menurun kembali pada perendaman 35 hari namun, nilainya masih diatas nilai viabilitas sel perendaman 16 hari. Perbedaan viabilitas sel antara kelompok breket Stainless Steel 17-4 PH lokal dan impor mungkin disebabkan oleh perbedaan metode pabrikasi dan komposisi yang digunakan antara kedua breket tersebut.

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Introduction: 17-4 PH Stainless Steel bracket is one of the most widely used brackets in the field of Orthodontics with long periods of time in the oral cavity. Its long use has caused a loss to the health of users due to the release of nickel and chromium ions due to the corrosion process. Therefore, the purpose of this study was to determine bracket cytotoxicity in gingival cells due to the release of nickel ions and chromium in artificial saliva. Methods: In Vitro research with 2 groups of local and imported 17-4 PH Stainless Steel brackets, each 24 brackets. Each group number of samples is divided into three based on immersion period in artificial saliva for 16, 28, and 35 days. Release of Cr and Ni ions in saliva from immersion brackets were exposed to gingival cells for cytotoxicity testing using MTT Assay. It can see how much cell viability indicates toxicity of brackets. Results: There are different cell viability patterns between local and imported 17- 4 PH Stainless Steel brackets, but statistically the cell viability difference is not significant, so there is no difference in cytotoxicity of local and imported 17-4 PH Stainless Steel brackets. Conclusion: Cytotoxicity test on local 17-4 PH Stainless Steel bracket shows cell viability pattern at immersion 16 days higher then when immersion 28 days it appears cell viability decreases and increases again at 35 days immersion while the cytotoxicity test on imported 17-4 PH Stainless Steel bracket showed a pattern of cell viability at 16 days soaking lower than 28 days immersion and decreased again at 35 days immersion, however the value is still above the 16-day immersion cell viability value. Differences in cell viability between groups of 17-4 PH Stainless Steel brackets local and imports maybe due to differences in manufacturing methods and the composition used between the two brackets."