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"Hidroksiapatit (HA) merupakan biomaterial yang dapat diekstrak dari limbah alami. Material hidroksiapatit dapat diaplikasikan dalam medis karena memiliki sifat biokompatibel, bioaktivitas, dan osteokonduksi yang bagus. Penelitian ini bertujuan untuk mensintesis hidroksiapatit dari tulang femur sapi dengan menggunakan suhu kalsinasi yang berbeda yaitu pada suhu 850^oC dan 900^oC. Hidroksiapatit yang diperoleh akan dikarakterisasi menggunakan Thermogravimetric Analysis (TGA), X-Ray Diffraction (XRD), Scanning Electron Microscopy Energy Dispersive Spectroscopy (SEM-EDS), dan Fourier Transform Infra Red (FTIR). Hasil karakterisasi menunjukkan bahwa semakin tinggi suhu kalsinasi maka akan semakin banyak senyawa organik yang terdekomposisi. Selain itu, peningkatan suhu kalsinasi menyebabkan ukuran kristal dan kristalinitas meningkat. Ukuran kristal HA sintesis meningkat dari 41,11 nm menjadi 57,50 nm dan derajat kristalinitas meningkat dari 87,34% menjadi 88,18%. HA sintesis dan HA komersial memiliki struktur kristal heksagonal yang menunjukkan bahwa rasio Ca/P tidak sesuai dengan stoikiometri. Rasio Ca/P yang diperoleh pada suhu kalsinasi 850^oC adalah 1,689 yang mana lebih mendekati rasio CaP stoikiometri 1,67 dibandingkan dengan menggunakan suhu kalsinasi 900^oC. Sedangkan HA komersial memiliki rasio Ca/P yang lebih rendah dibandingkan HA sintesis dengan nilai rasio 1,523.

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Hydroxyapatite (HA) is a biomaterial that can be extracted from natural waste. Hydroxyapatite can be applied medically because it has good biocompatibility, bioactivity, and osteoconduction. This study aims to synthesize hydroxyapatite from bovine bone using different calcination temperature, at 850^oC and 900^oC. Hydroxyapatite obtained will be characterized using Thermogravimetric Analysis (TGA), X-Ray Diffraction (XRD), Scanning Electron Microscopy Energy Dispersive Spectroscopy (SEM-EDS), and Fourier Transform Infra Red (FTIR). The results show that the higher temperature, the more organic compounds will be decomposed. In addition, an increase in calcination temperature causes crystallite size and crystallinity increased. Crystallite size of synthesis HA increased from 41.11 nm to 57.50 nm and the degree of crystallinity increased from 87.34% to 88.18%. Synthesis HA and commercial HA have a hexagonal crystal structure which means Ca/P ratio incompatible with stoichiometry. The Ca/P ratio obtained at temperature 850^oC is 1.689 which is closer to the stoichiometric Ca/P ratio 1.67 compared using temperature 900^oC. Whereas commercial HA has a lower Ca/P ratio than synthesis HA with ratio value 1.523."

"Fraktur tulang merupakan kondisi kerusakan pada sebagian atau seluruh kontinuitas tulang yang dapat menyebabkan beberapa komplikasi seperti infeksi, pendarahan, kerusakan pada saraf dan pembuluh darah, dan defek. graphine oxide/hidroksiapatit/fibrin, functionalized graphite/hidroksiapatit/fibrin, functionalized multiwalled carbon nanotubes/hidroksiapatit/fibrin, dan hidroksiapatit/fibrin perancah HAp/F memiliki ukuran pori 0,5 – 4,1 μm, GO/HAp/F 2,6 – 6,1 μm, fG/HAp/F 0,7 – 14,1 μm dan fMWCNT/HAp/F 1,5 – 11,1 μm. Terdapat gugus PO43- , O-H, C-H, C-O alifatik, dan amida I pada setiap kelompok perancah. Dengan penambahan gugus fungsi C=O pada perancah dengan penambahan material karbon. Nilai kekuatan tekan pada perancah GO/HAp/F, fG/HAp/F, dan fMWCNT/HAp/F sesuai dengan kekuatan tekan cancellous bone. Persentase porositas paling besar padaperancah GO/HAp/F sebesar 9,99 ± 2,85%. Perancah GO/HAp/F memiliki persentase swelling yang paling tinggi dan laju degradasi yang paling lambat. Sedangkan retensi yang paling baik ditunjukkan oleh perancah fG/HAp/F dengan persentase 8,27%. Berdasarkan keseluruhan hasil, perancah HAp/F dengan penambahan material GO mempunyai karakteristik fisika-kimia yang lebih baik pada penelitian ini dibandingkan dengan perancah fMWCNT atau fG.

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A fracture is a condition when the continuity of the bone is broken causing several complications such as infection, bleeding, damage to nerves and blood vessels, and disability. In this research, the solution offered is to fabricate a scaffold with a combination of biomaterials or composites in the form of graphine oxide/hydroxyapatite/fibrin, functionalized graphite/hydroxyapatite/fibrin, functionalized multiwalled carbon nanotubes/hydroxyapatite/fibrin, and hydroxyapatite/fibrin. Scaffolds were synthesized using the freeze-drying method. This study aims to determine the physico-chemical characteristics of the four groups of scaffolds. Based on the results of SEM-EDS, the HAp/F scaffold has a pore size of 0.5 – 4.1 μm, GO/HAp/F has 2.6 – 6.1 μm, fG/HAp/F has 0.7 – 14.1 μm and fMWCNT/HAp/F has 1.5 – 11.1 μm. There were PO43- , O-H, C-H, aliphatic C-O and amide I groups in each scaffold. Additionally the C=O functional group on the scaffold with the addition of carbon material. The compressive strength values of GO/HAp/F, fG/HAp/F, and fMWCNT/HAp/F scaffolds correspond to the compressive strength of the cancellous bone. The highest percentage of porosity is GO/HAp/F scaffolds with 9.99 ± 2.85%. GO/HAp/F scaffolds had the highest swelling percentage and the slowest degradation rate. Meanwhile, the best retention was shown by fG/HAp/F scaffold with a percentage of 8.27%. Based on the overall results, the HAp/F scaffold with the addition of GO material had better physico-chemical characteristics in this study than fMWCNT or fG scaffolds."

"[ABSTRAKHidroksiapatit (HA) mempunyai peran penting dalam bidang medis karena komposisi kimia dan strukturnya yang mirip dengan tulang manusia. Material ini disintesis melalui metode hidrotermal dengan prekusor Ca(NO3)2, CaO dan NH3PO4. Variasi temperatur hidrotermal pada 150 ̊C dan 300 ̊C, temperatur sintering pada 900 ̊C selama 3 jam. Endapan yang diperoleh diuji dengan XRD dan SEM-EDX. Morfologi partikel hasil karakterisasi SEM berbentuk batangan memanjang dan melingkar teraglomerasi dan hasil uji EDX menunjukkan rasio Ca/P yang lebih besar dari 1.67. Uji XRD menunjukkan adanya fasa kalsium difosfat, fluorapatit dan apatit karbonat tipe- A di dalam endapan yang meningkatkan rasio Ca/P.ABSTRACTHydroxyapatite (HA) posseses significant role in medical application due to its similarity in chemical and structure to human bones. This material was synthesized through hydrothermal method using Ca(NO3)2, CaO and NH3PO4. Hydrothermal temperature varied on 150 ̊C and 300 ̊C, sintering temperature on 900 ̊C for 3 hours. Sample was characterization by XRD and SEM-EDX. Morphology observed by SEM is agglomerated round- spherical- shape particle with Ca/P ratio more than 1.67 measured by EDX. Calcium diphospate, fluorapatite and carbonated type- A presence is observed by XRD.;Hydroxyapatite (HA) posseses significant role in medical application due to its similarity in chemical and structure to human bones. This material was synthesized through hydrothermal method using Ca(NO3)2, CaO and NH3PO4. Hydrothermal temperature varied on 150 ̊C and 300 ̊C, sintering temperature on 900 ̊C for 3 hours. Sample was characterization by XRD and SEM-EDX. Morphology observed by SEM is agglomerated round- spherical- shape particle with Ca/P ratio more than 1.67 measured by EDX. Calcium diphospate, fluorapatite and carbonated type- A presence is observed by XRD., Hydroxyapatite (HA) posseses significant role in medical application due to its similarity in chemical and structure to human bones. This material was synthesized through hydrothermal method using Ca(NO3)2, CaO and NH3PO4. Hydrothermal temperature varied on 150 ̊C and 300 ̊C, sintering temperature on 900 ̊C for 3 hours. Sample was characterization by XRD and SEM-EDX. Morphology observed by SEM is agglomerated round- spherical- shape particle with Ca/P ratio more than 1.67 measured by EDX. Calcium diphospate, fluorapatite and carbonated type- A presence is observed by XRD.]"

"Potensi sampah biologi seperti tulang sapi di Indonesia cukup besar ketersediaannya, dan dapat digunakan sebagai sumber hidroksiapatit (BHA) dalam aplikasi biomedik yang ekonomis dan ramah lingkungan. Penelitian ini melakukan preparasi hidroksiapatit menggunakan penggabungan tiga metode yaitu mekanik, ultrasonik dan spray drying untuk menghasilkan hidroksiapatit dengan distribusi ukuran yang seragam. Preparasi bahan baku dilakukan dengan dan tanpa proses kalsinasi. Metode ultrasonik dilakukan dengan variasi pelarut, aquabides dan etanol dengan variasi waktu sonikasi 20, 40, 60 dan 180 menit dan dilanjutkan dengan spray drying. Karakterisasi BHA menggunakan PSA, FTIR dan XRD. BHA dengan kristalinitas tinggi dan distribusi ukuran yang seragam tercapai pada metode ultrasonik pada media aquabides dengan kalsinasi.

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Bovine bone biowaste is potential as a source of hydroxyapatite (BHA), thus it is necessary to preparation by simple and environmentally friendly. In the present study investigated the preparation and characterization of hydroxyapatite from bovine bone by combination methods of mechanical, ultrasonic and spray drying to produce hydroxyapatite with homogenous distibution size, high efficiency, and also high reproducibility. We also investigated the types of solvents and ultrasonic times to evaluate the particle size of HA. Preparation was done in two difference phases, with and without calcination process.

Ultrasonic method is performed by variation of solvent, ethanol and aquabides with sonication time 20, 40, 60 and 180 minutes and followed by spray drying. BHA was characterization with PSA, FTIR and XRD. BHA that have high crystallinity, uniform size and distribution is achieved by the ultrasonic method with calcination in aquabides."

"ABSTRAKPendahuluan.Hidroksiapatit sintesis dan hidroksiapatit (HA) yang diproleh secara komersial menunjukkan derajad kristalinitas tinggi. Salah satu usaha untuk meningkatkan kemampuan degradasi scaffold alginat/HA adalah menggunakan HA amorf dan dalam struktur komposit biopolimer/HA. Alginat yang diperoleh dari alga coklat Sargassum di perairan Banten belum dimanfaatkan untuk kegunaan rekayasa jaringan. Selain itu, pengamatan pertumbuhan sel pada scaffold selalu dilakukan pada scaffold yang materialnya diperoleh secara komerisal.Tujuan.Tujuan dari penelitian ini adalah untuk memperoleh scaffold dari komposit hidroksiapatit kalsinasi rendah dengan alginat (S.duplicatum dan S.crassifolium) yang dapat digunakan sebagai kerangkat pertumbuhan sel.Material dan Metode.Scaffold dipreparasi dari HA yang diperoleh secara sintesis dengan alginat yang ekstraksi dari alga S.duplicatum atau S.crassifolium. Karakterisasi dilakukan terhadap serbuk HA dengan kalsinasi suhu 400°-900°C , serbuk alginat dan scaffold alginat S.duplicatum/HA atau S.crassifolium/HA. Pemilihan dengan kemampuan degradasi tinggi selain berdasarkan berdasarkan derajat kristalinitas, ukuran kristalit dan luas mukaHA, juga berdasarkan uji degradasi dan uji mekanik dari scaffold. Selanjutnya, terhadap scaffold alginat S.duplicatum dan S.crassifolium/HA dilakukan kultur sel. Pertumbuhan sel diukur dari aktifitas ALP dan perlekatan sel pada scaffold.Hasil.Serbuk hidroksiapatit dengan kalsinasi suhu 400°C, 750°C atau 900°C telah diidentifikasi sebagai fasa hidroksiapatit karbonasi yang sesuai dengan tulang. Identifikasi terhadap alginat S.duplicatum atau S.crassifolium memperlihatkan terbentuknya alginat yang mengandung gugus yang sesuai dengan protein. Hidroksiapatit kalsinasi suhu 400°C menunjukkan degradasi terbesar. Namun, mempertimbangkan kekuatan mekanik, telah dipilih scaffold alginat S.duplicatum/HA750°C dan S.crassifolium/ HA750°C untuk dilakukan kultur sel punca mesenkimal. Pengamatan setelah lima minggu pada masingmasing scaffold diketahui bahwa sel punca mesenkim telah berdiferensiasi ke ostoeblas dan memperlihatkan perlekatan osteoblas pada masing-masing scaffold. Pembahasan.Pertumbuhan sel punca mesenkimal pada scaffold komposit alginat S.duplicatum/HA750°C dan S.crassifolium/ HA750°C dapat dijelaskan karena adanya degradasi dari material scaffold selama scaffold berada di dalam medium kultur. Degradasi memungkinkan terlepasnya ion-ion yang terkandung di dalam material scaffold dan masuk ke dalam sel serta mempengaruhi pertumbuhan sel punca mesenkimal.

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ABSTRACTIntroduction.Synthesized and commercially available hydroxyapatites have shown high degree of crystallinity which were difficult to degrade. Efforts to incrrease the degradation have used amorphous hydroxyapatite and alginate/hydroxyapatite structure. As an addition, the abundant of Sargassum algae in Banten shore have not been applied for tissue engineering purposes. The use of mesenchymal stem cell have showed more proliferation in scaffold than that of osteoblasts.Aim.The aims of the present study, therefore, were to provide alginat / hydroxyapatites of low calcination temperatures compsite scaffolds available for mesenchymal stem cell growth.Materials and Methods.Alginate/hydroxyapatite composite scaffolds were developed using S.duplicatum or S.crassifolium with amorphous hydroxyapatites. Characterizations were conducted for S.duplicatum or S.crassifolium alginates, hydroxyapatites as well as alginate/hydroxyapatite composite scaffolds. Alginat/ hydroxyapatite composite showing high degradation and high compressive strength were considered for cell culture in the scaffolds.Results.Results showed that extractions of S.duplicatum and S.crassifolium algae were identified as alginates presenting the components similar to proteins. Synthesized hydroxyapatites calcinated at 400°C, 750°C or 900°C was identified as carbonated hydroxyapatite that simulate the human hard tissues. Hydroxyapatite of 400°C showed higher degradation. However, alginate S.duplicatum/hydroxyapatite of 750°C and S.crassifolium/ hydroxyapatite of 750°C composites scaffolds were chosen as scaffolds for the cell culture to secure the compression strength. Incubation of mesenchymal stem cells on both scaffolds for five weeks have showed differentiation of mesenchymal stem cells into osteoblasts and cell attachment in each scaffolds.Discussion.The growth of osteoblast in alginate S.duplicatum/hydroxyapatite of 750°C and S.crassifolium/ hydroxyapatite of 750°C composites scaffolds may have been due to the degradation each scaffolds that would transfer ions from the scaffolds to mesenchymal stem cells."

"[ABSTRAKHroksiapatit merupakan jenis biomaterial sintetis yang mempunyai fasa yang paling stabil dibandingkan dengan senyawa kalsiun fosfat lainnya, selain itu hidroksiapatit memiliki tingkat kemiripan yang tinggi dengan tulang, sehingga hidroksiapatik banyak diaplikasikan sebagai bone graft sintetis. Tujuan dari penelitian ini adalah untuk mengetahui pengaruh waktu sintering terhadap kemurnian kristal hidroksiapatit yang dihasilkan. Hidroksiapatit dari prekursor kimia CaCO3 dan (NH4)2HPO4 disintesis dengan menggunakan metode hidrotermal pada temperatur 150oC dan 300oC. Hasil dari sintesis hidroksiapatik dikarakterisasi dengan menggunakan X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), dan Energy Dispersive Analysis X-Ray (EDX). Hasil karakterisasi XRD memperlihatkan intensitas tertinggi rata-rata berada pada sudut 2θ yaitu, 25.898o, 31.789o, 32.216o, 32.922o, 46.729o, dan 49.524o. Hasil dari SEM memperlihatkan morfologi dari sampel bebrbetuk nanoroot dan hasil dari EDX menunjukan rasio Ca/P sebesar 1.8.ABSTRACTHydroxyapatite is the most phase-stable syntetic biomaterial compared to another calcium phospate material. Hydroxyapatite also has high similarity with bone which make it has wide application as syntetic bone graft. Purpose of this research is to study the effect of sintering time towards hydroxyapatite crystal?s purity. Hydroxyapatite made from chemical precursor CaCO3 and (NH4)2HPO4 was synthesized using hydrothermal method on 150oC and 300oC. Synthesized hydroxyapatite was characterized using X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Energy Dispersive Analysis X-Ray (EDX). The result of characterization showed that highest average intensity on 2θ were: 25.898o, 31.789o, 32.216o, 32.922o, 46.729o, and 49.524o.;Hydroxyapatite is the most phase-stable syntetic biomaterial compared to another calcium phospate material. Hydroxyapatite also has high similarity with bone which make it has wide application as syntetic bone graft. Purpose of this research is to study the effect of sintering time towards hydroxyapatite crystal?s purity. Hydroxyapatite made from chemical precursor CaCO3 and (NH4)2HPO4 was synthesized using hydrothermal method on 150oC and 300oC. Synthesized hydroxyapatite was characterized using X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Energy Dispersive Analysis X-Ray (EDX). The result of characterization showed that highest average intensity on 2θ were: 25.898o, 31.789o, 32.216o, 32.922o, 46.729o, and 49.524o.;Hydroxyapatite is the most phase-stable syntetic biomaterial compared to another calcium phospate material. Hydroxyapatite also has high similarity with bone which make it has wide application as syntetic bone graft. Purpose of this research is to study the effect of sintering time towards hydroxyapatite crystal?s purity. Hydroxyapatite made from chemical precursor CaCO3 and (NH4)2HPO4 was synthesized using hydrothermal method on 150oC and 300oC. Synthesized hydroxyapatite was characterized using X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Energy Dispersive Analysis X-Ray (EDX). The result of characterization showed that highest average intensity on 2θ were: 25.898o, 31.789o, 32.216o, 32.922o, 46.729o, and 49.524o., Hydroxyapatite is the most phase-stable syntetic biomaterial compared to another calcium phospate material. Hydroxyapatite also has high similarity with bone which make it has wide application as syntetic bone graft. Purpose of this research is to study the effect of sintering time towards hydroxyapatite crystal’s purity. Hydroxyapatite made from chemical precursor CaCO3 and (NH4)2HPO4 was synthesized using hydrothermal method on 150oC and 300oC. Synthesized hydroxyapatite was characterized using X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Energy Dispersive Analysis X-Ray (EDX). The result of characterization showed that highest average intensity on 2θ were: 25.898o, 31.789o, 32.216o, 32.922o, 46.729o, and 49.524o.]"

"Gangguan dan penyakit tulang merupakan hal yang mengkhawatirkan karena prevalensinya yang meningkat. Rekayasa jaringan tulang dengan pengembangan struktur melalui kombinasi perancah, sel, dan/atau faktor biologis merupakan solusi yang menjanjikan untuk regenerasi tulang. Kolagen dan hidroksiapatit termasuk bahan perancah yang paling umum digunakan untuk rekayasa jaringan tulang dan dapat diekstraksi dari sumber alam. Indonesia sebagai negara kepulauan terbesar dan produsen ikan terbesar kedua di dunia, memiliki sumber daya laut yang melimpah. Perikanan tuna yang termasuk paling besar dan paling produktif di dunia menghasilkan produk sampingan dengan jumlah yang besar. Pada penelitian ini, kolagen dan hidroksiapatit diekstraksi dari produk sampingan tuna, yaitu tulang kerangka dan kepala, menggunakan ekstraksi pelarutan asam untuk kolagen dan kalsinasi untuk hidroksiapatit. Kolagen hasil ekstraksi dikarakterisasi menggunakan UV-Vis spectrophotometry, FTIR, dan SEM-EDX, sedangkan hidroksiapatit hasil ekstraksi dikarakterisasi menggunakan FTIR, SEM-EDX, dan XRD. Berdasarkan hasil karakterisasi, kolagen hasil ekstraksi memiliki puncak absorbansi di 225 nm, memiliki struktur heliks rangkap tiga, struktur mikro lembaran berlapis, berpori, dan sedikit berkerut. Sedangkan hidroksiapatit hasil ekstraksi memiliki ukuran dan bentuk partikel bervariasi dengan ukuran kristal 16,64 nm, 15,62 nm, 16,63 nm, 4,39 nm, crystallinity index 0,643, 0,572, 0,613, 0,027, dan nilai Ca/P 1,753±0,052, 1,806±0,074, 1,792±0,021, 1,935±0,091 masing-masing untuk sampel kalsinasi 1, sampel kalsinasi 2, sampel kalsinasi 3, dan sampel ultrasonikasi. Kolagen hasil ekstraksi dapat dikembangkan sebagai bahan perancah tulang karena memliki struktur berpori yang dibutuhkan untuk penetrasi sel, nutrisi dan transfer limbah, serta angiogenesis; sedangkan hidroksiapatit sampel kalsinasi 1 memiliki nilai rasio Ca/P (1,753±0,052) yang paling mendekati rasio Ca/P pada tulang manusia (1,67). Ekstraksi kolagen dan hidroksiapatit ini diharapkan dapat memanfaatkan produk sampingan sumber daya laut dan dapat digunakan sebagai material perancah tulang untuk mengatasi gangguan dan penyakit tulang.

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Bone disorders and diseases are a matter of concern because of their increasing prevalence. Bone tissue engineering with structural development through a combination of scaffolds, cells, and/or biological factors is a promising solution for bone regeneration. Collagen and hydroxyapatite are among the most commonly used scaffold materials for bone tissue engineering and can be extracted from natural sources. Indonesia is the largest archipelagic country and the second-largest fish producer in the world, has abundant marine resources. Tuna fisheries, which are among the largest and most productive in the world, produce large amounts of by-products. In this study, collagen and hydroxyapatite were extracted from tuna by-products, including skeleton and head, using acid solubilization extraction for collagen and calcination for hydroxyapatite. The extracted collagen was then characterized using UV-Vis spectrophotometry, FTIR, and SEM-EDX, while the extracted hydroxyapatite was characterized using FTIR, SEM-EDX, and XRD. Based on the characterization results, the extracted collagen has an absorbance peak at 225 nm, has a triple-helix structure, a layered sheet microstructure, is porous, and is slightly wrinkled. While the extracted hydroxyapatite has various particle sizes and shapes with crystal sizes of 16.64 nm, 15.62 nm, 16.63 nm, 4.39 nm, crystallinity index 0.643, 0.572, 0.613, 0.027, and Ca/P values were 1.753±0.052, 1.806±0.074, 1.792±0.021, 1.935±0.091 for the calcined sample 1, calcined sample 2, calcined sample 3, and ultrasonicated sample, respectively. Extracted collagen can be developed as a bone scaffold material because it has a porous structure required for cell penetration, nutrition and waste transfer, and angiogenesis; while the hydroxyapatite of calcined sample 1 has a Ca/P ratio value (1.753±0.052) which is closest to the Ca/P ratio in human bone (1.67). The extraction of collagen and hydroxyapatite is expected to be able to utilize marine by-products and can be used as bone scaffold material to treat bone disorders and diseases."

"Latar Belakang: Perbaikan defek tulang dapat dilakukan dengan penggunaan material bone graft. Secara klinis, material bone graft dipakai dalam berbagai variasi ukuran granul yang disesuaikan dengan pertimbangan untuk aplikasi spesifik dan tujuan penggunaan bone graft. Di sisi lain, informasi mengenai pengaruh ukuran granul bone graft belum diketahui dan belum ada penelitian mengenai efek perbedaan ukuran granul pada prototipe karbonat hidroksiapatit terhadap kelarutan in vitro dan sitotoksisitas. Tujuan: Mengevaluasi pengaruh ukuran granul terhadap kelarutan in vitro dan sitotoksisitas prototipe karbonat hidroksiapatit. Metode: Uji kelarutan in vitro dengan merendam prototipe karbonat hidroksiapatit dalam larutan asetat buffer dan Tris-HCl buffer selama 7 hari dalam suhu 37°C. Nilai kelarutan in vitro diuji dengan alat Horiba Ion Selective Electrode. Uji sitotoksisitas dengan MTT Assay pengaruh medium ekstrak terhadap sel preosteoblas MC3T3-E1 selama 1 hari. Nilai absorbansi dibaca dengan ELISA Microplate Reader. Analisis data dengan uji statistik One-Way ANOVA. Hasil: Konsentrasi ion kalsium terlarut dalam larutan asetat buffer pada kelompok ukuran granul 250-500 µm yaitu 45,79 ± 3,11 mg/L, 500-1000 µm yaitu 37,41 ± 4,28 mg/L, dan 1000-2000 µm yaitu 35,85 ± 1,28 mg/L. Konsentrasi ion kalsium terlarut dalam larutan Tris-HCl buffer pada kelompok ukuran granul 250-500 µm yaitu 3,88 ± 0,36 mg/L, 500-1000 µm yaitu 2,94 ± 0,19 mg/L, dan 1000-2000 µm yaitu 2,02 ± 0,58 mg/L. Uji statistik menunjukkan perbedaan konsentrasi ion kalsium terlarut yang signifikan antara granul ukuran 250-500 µm dan 1000-2000 µm pada kedua larutan buffer. Persen viabilitas sel menunjukkan hasil diatas 70% pada semua kelompok ukuran granul dan konsentrasi ekstrak. Uji statistik menunjukkan perbedaan nilai absorbansi dan persen viabilitas sel pada konsentrasi ekstrak 50 mg/mL prototipe karbonat hidroksiapatit ukuran 250-500 µm terhadap 1000-2000 µm, 100 mg/mL prototipe karbonat hidroksiapatit ukuran 250-500 µm terhadap 500-1000 µm, dan konsentrasi ekstrak 200 mg/mL prototipe karbonat hidroksiapatit ukuran 250-500 µm terhadap 1000-2000 µm dan 500-1000 µm terhadap 1000-2000 µm. Kesimpulan: Semakin besar ukuran granul prototipe karbonat hidroksiapatit yang direndam dalam larutan asetat buffer dan Tris-HCl buffer, hasil uji kelarutan in vitro menunjukkan.rata-rata konsentrasi ion kalsium terlarut yang semakin kecil. Uji sitotoksisitas prototipe karbonat hidroksiapatit menunjukkan hasil nontoksik dengan viabilitas sel ukuran granul 1000-2000 µm>500-1000 µm>250-500 µm.

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Background: Repair of bone defects can be done using bone graft material. Clinically, bone graft material is used in a variety of granule sizes that are adjusted to consider the specific application and intended use of the bone graft. On the other hand, information regarding the influence of bone graft granule size is not yet known and there has been no research regarding the effect of differences in granule size in hydroxyapatite carbonate prototypes on in vitro solubility and cytotoxicity. Objective: To evaluate the effect of granule size on the in vitro solubility and cytotoxicity of the carbonate hydroxyapatite prototype. Methods: The in vitro solubility test was conducted by immersing the carbonate hydroxyapatite prototype in a solution of acetate buffer and Tris-HCl buffer for 7 days at a temperature of 37°C. The in vitro solubility value was tested using the Horiba Ion Selective Electrode. The cell cytotoxicity test was carried out using MTT assay for the effect of medium extracts on MC3T3-E1 preosteoblast cells. Absorption values were read with an ELISA Microplate Reader. Data analysis using the One-Way ANOVA statistical test. Results: The concentration of dissolved calcium ions in the acetate buffer solution in the granule size group 250-500 µm was 45.79 ± 3.11 mg/L, 500-1000 µm was 37.41 ± 4.28 mg/L, and 1000-2000 µm was 35, 85 ± 1.28mg/L. The concentration of dissolved calcium ions in the Tris-HCl buffer solution in the granule size group 250-500 µm was 3.88 ± 0,36 mg/L, 500-1000 µm was 2.94 ± 0.19 mg/L, and 1000-2000 µm was 2, 02 ± 0.58mg/L. Statistical tests showed significant differences in dissolved calcium ion concentrations between granules measuring 250-500 µm and 1000-2000 µm in both buffer solutions. The percentage of cell viability showed results above 70% in all granule size groups and extract concentrations. Statistical tests show differences in absorption values and percent cell viability at extract concentrations of 50 mg/mL of carbonate hydroxyapatite prototype with a size of 250-500 µm versus 1000-2000 µm, 100 mg/mL hydroxyapatite carbonate prototype with a size of 250-500 µm versus 500-1000 µm, and extract concentration 200 mg/mL carbonate hydroxyapatite prototype size 250-500 µm against 1000-2000 µm and 500-1000 µm against 1000-2000 µm. Conclusion: The larger the size of the carbonate hydroxyapatite prototype granules soaked in acetate buffer and Tris-HCl buffer, the results of the in vitro solubility test show a smaller average concentration of dissolved calcium ions. The cytotoxicity test of the carbonate hydroxyapatite prototype showed nontoxic results with cell viability of granule size 1000-2000 µm > 500-1000 µm > 250-500 µm."

"Hidroksiapatit (HA) merupakan salah satu material bone graft alloplast yang sering digunakan dalam prosedur bone grafting karena sifat osteokonduktif dan biokompatibel yang baik serta komposisinya yang mirip dengan komponen anorganik tulang dan gigi. Namun, HA yang diproduksi dengan metode sintering sulit teresorpsi di dalam tubuh karena kristalinitas yang tinggi. HA dengan kristalinitas rendah dapat diproduksi dengan metode disolusi presipitasi. Pembuatan HA dalam bentuk blok membutuhkan waktu lebih lama dibandingkan granul, penambahan kondisi hidrotermal dapat mempercepat waktu konversi. Penelitian ini bertujuan untuk menganalisis kekuatan tekan HA yang dihasilkan dari blok gipsum yang direndam dalam larutan Na3PO4 1 mol/L pada kondisi hidrotermal selama 48 jam pada suhu 100oC dan 140oC dan 180oC dan. Blok gipsum dibuat dengan mencampurkan bubuk kalsium sulfat hemihidrat dan aquades dengan rasio akuades dibanding bubuk 0,5. Blok gipsum direndam di dalam larutan Na3PO4 1 mol/L dan dipanaskan selama 48 jam pada suhu 100oC, 140oC dan 180oC. Uji compressive strength dilakukan untuk evaluasi kuat tekan dengan menggunakan Universal Testing Machine AGS-X (Shimadzu, Japan). Setelah perendaman, HA teridentifikasi pada semua kelompok spesimen, namun pada kelompok 100oC dan 140oC selain HA, fasa gipsum juga masih teridentifikasi. Pada kelompok 180oC hanya HA yang teridentifikasi. Berdasarkan uji statistik One-Way ANOVA dan Post-Hoc Tamhane, terdapat penurunan nilai kuat tekan yang signifikan antara kelompok kontrol (gipsum) dan setelah perlakuan suhu 100oC, 140oC dan 180oC. Penurunan nilai kuat tekan juga signifikan antara kelompok perlakuan suhu 180oC dengan kelompok perlakuan suhu 100oC dan 140oC. Namun, tidak ada perbedaan bermakna nilai kuat tekan antara kelompok perlakuan suhu 100oC dan 140oC. Disimpulkan bahwa penelitian ini menunjukkan nilai kekuatan tekan yang turun secara signifikan dibandingkan dengan kelompok kontrol (gipsum).

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Hydroxyapatite (HA) is one of the alloplastic materials that is often used in bone grafting procedures because of its osteoconductive and biocompatible properties and its composition which is similar to the inorganic components of bones and teeth. However, sintered HA cannot be reabsorbed in the body due to its high crystallinity. Low crystalline HA can be fabricated through dissolution-precipitation reaction. HA block require conversion time that HA granules. Applying hydrothermal condition to dissolution-precipitation reaction would compensate for longer conversion time. The aim of this study was to analyze the compressive strength of HA block produced from gypsum block that immersion in Na3PO4 1 mol/L solution based on dissolution precipitation method under hydrothermal condition. Block gypsum were made from calcium sulfate hemihydrate powder mixed with distilled water at water to powder ratio 0,5. The gypsum blocks were immersed in Na3PO4 1 mol/L solution for 48 hours at 100oC, 140oC and 180oC. Compressive strength test was used for mechanical strength evaluation and was done with Universal Testing Machine AGS-X (Shimadzu, Japan). After immersion, there was a HA phase identified in all groups, however, groups that had immersion at 100oC and 140oC there was gypsum identified too. Based on statistical analysis using One Way ANOVA and Post-Hoc Tamhane test, there was a significant decrease in compressive strength value between groups of specimens before and after immersion at 100oC, 140oC and 180oC. Compressive strength value was Also significant between group immersion at 180oC and 100oC, 140oC. But the difference between the group after immersion at 100oC and 140oC was not significant. It was concluded that the compressive strength value decreased significantly compared to the control group (gypsum)."