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"Latar Belakang: Remineralisasi dentin dapat dicapai melalui beberapa metode, diantaranya secara Guided Tissue Remineralization (GTR) dalam sistem Polymer-Induced Liquid Precursor (PILP). Remineralisasi secara GTR terbukti dapat meremineralisasi affected dentin dengan membentuk mineral intrafibrillar dan ekstrafibrillar. Melalui sistem PILP, kristal terbentuk dengan ukuran kecil sehingga remineralisasi lebih banyak terjadi secara intrafibrillar. Penambahan fluor dalam sistem PILP diharapkan dapat membentuk kristal fluoroapatit yang berukuran lebih besar dan mampu menyempurnakan remineralisasi hingga ke ekstrafibrillar. Penelitian yang ada selama ini hanya berfokus pada permukaan dentin, sedengkan belum terdapat penelitian untuk membuktikan remineralisasi dengan penambahan fluor yang terjadi pada dinding tubulus dentin. Tujuan: Mengetahui pengaruh penambahan fluor 5ppm dan 25ppm dalam sistem PILP terhadap perubahan topografi dinding tubulus dentin dan persentase fluoroapatit. Metode: Sampel blok dentin terdemineralisasi direndam pada larutan remineralisasi dengan penambahan 5ppm dan 25ppm fluor. Sampel blok dentin kemudian akan dipotong lintang menggunakan metode fraktur lalu diamati dan dianalisis menggunakan uji FE-SEM dan XRD. Hasil: Terjadi perubahan topografi pada dinding tubulus dentin setelah dilakukan remineralisasi melalui proses PILPdengan penambahan 5ppm dan 25ppm fluor selama 14 hari yang dievaluasi secara deskriptif menggunakan FE-SEM. Hasil analisis XRD menunjukkan tidak ada perbedaan bermakna secara statistik penambahan fluor pada larutan remineralisasi PILP terhadap persentase fasa mineral fluoroapatit, namun secara substansi terjadipeningkatan persentase fluorapatit. Kesimpulan: Penambahan fluor dalam sistem PILP berpengaruh terhadap perubahan topografi dinding tubulus dentin dan persentasefluoroapatit.

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Background: Dentine remineralization can be achieved through several methods,

including Guided Tissue Remineralization (GTR) in the Polymer-Induced Liquid

Precursor (PILP) system. GTR remineralization has been shown to remineralize

affected dentin by forming intrafibrillar and extrafibrillar minerals. Through the PILP

system, crystals are formed with small sizes so that more remineralization occurs

intrafibrillarly. The addition of fluorine in the PILP system is expected to form larger

fluoroapatite crystals and be able to complete the remineralization to extrafibrillar. Existing research so far has only focused on the dentin surface, although there has been no research to prove remineralization with the addition of fluorine that occurs in the dentine tubule walls. Objective: To determine the effect of adding 5ppm and 25ppm fluorine in the PILP system on changes in the topography of the dentinal tubule walls and the percentage of fluoroapatite. Methods: Demineralized dentine block samples were immersed in remineralization solution with the addition of 5 ppm and 25 ppm fluorine. The dentine block samples will then be cross-sectioned using the fracture method and then observed and analyzed using the FE-SEM and XRD tests. Results: Topographical changes occurred in the dentinal tubule walls after remineralization through the PILP process with the addition of 5ppm and 25ppm fluorine for 14 days which were evaluated descriptively using FE-SEM. The results of the XRD analysis showed that there was no statistically significant difference in the addition of fluorine to the percentage of fluoroapatite mineral phase in the addition of fluorine to the percentage of fluoroapatite, but in substance there was an increase in the percentage of fluorapatite. Conclusion: The addition of fluorine in the PILP system affected the topography of the dentinal tubule walls and the percentage of fluoroapatite."

"Latar Belakang : Remineralisasi Guided Tissue Remineralization (GTR) dentin digunakan untuk meningkatkan pembentukan kristal nano ke daerah gap zone serta membangun struktur mineral apatit pada kolagen demineralized dentin dan Carboxymethyl Chitosan (CMC) berperan sebagai protein analog serta memicu remineralisasi dentin. Tujuan: Mendapatkan novel semen carboxymethyl chitosan/amporphous calcium phosphate sebagai agen GTR dentin. Metode: Modifikasi CMC menjadi bubuk CMC/ACP (CA) melalui proses Freeze Dry dan modifikasi bubuk CA melalui proses milling 30 menit menjadi bubuk CMC/ACP paska milling (CAM) dan masing-masing dievaluasi menggunakan FTIR menganalisis gugus fungsi CMC dan gugus fungsi awal CA yang terbentuk. Bubuk CA dan CAM kemudian dicampurkan dengan gipsum hemihydrate pada rasio 5% dan 10% didapatkan kelompok novel semen CAG 5%, CAG 10%, CAMG 5% dan CAMG 10%. Kelompok tersebut dievaluasi menggunakan FTIR, XRD, SEM, setting time, ketahanan kompresi dan MTT assay. Novel semen tersebut diaplikasikan pada dentin terdemineralisasi selama 14 hari dan dievaluasi menggunakan TEM. Hasil: Gugus fungsi CMC berupa -CH2COOH dan N-H terlihat pada bubuk CA dan setelah dilakukan milling menjadi bubuk CAM. Tambahan gugus fungsi fosfat (-PO4) terlihat juga pada bubuk CA dan CAM. Gugus fungsi awal bubuk CA tetap terlihat pada bubuk CAM. Gugus fungsi fosfat (-PO4) terlihat juga pada kelompok novel semen CAG dan CAMG baik 5% dan 10%. Kombinasi bubuk CA dan CAM menggunakan gipsum mempengaruhi fasa mineral material. Kesan topografi berbeda pada novel semen CAG (5% dan 10%) dan novel semen CAMG (5% dan 10%). Terdapat perbedaan bermakna antara kelompok novel semen (CAG 5%, CAG 10%, CAMG 5% dan CAMG 10%) dibandingkan dengan gipsum (kontrol) pada setting time dan ketahanan kompresi (p<0.05). Viabilitas sel dari uji MTT assay menunjukkan novel semen CAMG 10% tidak toksik terhadap hDPSC. Novel semen CAG (5% dan 10%) dan novel semen CAMG (5% dan 10%) menunjukkan kesan remineralisasi dentin ekstrafibrillar dan intrafibrillar pada dentin terdemineralisasi. Kesimpulan: Modifikasi carboxymethyl chitosan melalui proses freeze dry dan milling serta pencampuran rasio 5% dan 10% menggunakan gipsum memiliki kemampuan untuk menginisiasi guided tissue remineralisazation dentin baik secara ekstrafibrillar dan intrafibrillar pada dentin terdemineralisasi.

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Background: Guided Tissue Remineralization (GTR) dentin is used to increase the formation of nanocrystals in the gap zone area and build an apatite mineral structure in demineralized dentin collagen and Carboxymethyl Chitosan (CMC) which acts as a protein analog and triggers dentin remineralization. Objective: To obtain a novel carboxymethyl chitosan/amorphous calcium phosphate cement as a dentinal GTR agent.Purpose: Obtained novel cement carboxymethyl chitosan/amporphous calcium phosphate as an agent for GTR. Methods: Modification of CMC into CMC/ACP (CA) powder through the Freeze Dry process and modification of CA powder through a 30-minute milling process into CMC/ACP powder after milling (CAM) and evaluated using FTIR, respectively, analyzing the CMC functional group and the initial CA functional group formed. CA and CAM powder were then mixed with gypsum hemihydrate at a ratio of 5% and 10% to obtain novel cement groups of CAG 5%, CAG 10%, CAMG 5%, and CAMG 10%. The groups were evaluated using FTIR, XRD, SEM, setting time, compression resistance, and MTT assay. The novel cement was applied to demineralized dentin for 14 days and evaluated using TEM. Result: The CMC functional group (-CH2COOH and N-H) was seen in CA and CAM powder. Addition of phosphate (-PO4) functional grup were detected in CA and CAM powder. Phosphate (-PO4) functional group was seen in novel cement CAG (5% and 10%) and CAMG (5% and 10%). The combination of gipsum using CA and CAM powders produces different mineral phases. Topographical impressions differed between Novel cement groups of CAG (5% and 10%) and CAMG (5% and 10%). There was a significant difference between the novel cement groups (CAG 5%, CAG 10%, CAMG 5%, and CAMG 10%) compared to gypsum (control) in setting time and compression resistance (p<0.05). Viability cell confirmation using MTT assay showed that novel cemen group of CAMG 10% did not toxic to hDPSC. Novel cement groups of CAG (5% and 10%) and CAMG (5% and 10%) demonstrated the effects of extrafibrillar and intrafibrillar dentin remineralization on demineralized dentin. Conclusion: Modifying carboxymethyl chitosan through freeze dry and milling processes and modifying the mixing ratio of 5% and 10% using gypsum can initiate guided tissue remineralization of dentin both extrafibrillarly and intrafibrillarly in demineralized dentin."

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Latar Belakang: Perawatan karies dengan minimal intervensi, yaitu dengan membuang infected dentin, dan meninggalkan affected dentin, kemudian dilakukan remineralisasi pada affected dentin. Pada affected dentin masih terdapat ikatan silang kolagen. Remineralisasi dentin lebih kompleks karena pada karies dentin sudah tidak ada sisa kristal mineral. Untuk terjadinya remineralisasi ekstrafibrilar dan intrafibrilar pada dentin, maka dibutuhkan dentin matrix protein 1 (DMP 1)  yang merupakan protein non-kolagen. Proses polymer-induced liquid precursor (PILP) merupakan metode Guided Tissue Remineralization yang bertujuan untuk remineralisasi dentin secara intrafibrilar dan ekstrafibrilar dengan penambahan polimer sebagai analog DMP1. Salah satu material analog protein non kolagen adalah asam poliaspartik.

Tujuan: Mengevaluasi remineralisasi dentin pada permukaan demineralized dentin setelah perendaman dengan larutan remineralisasi yang mengandung asam poliaspartik sebagai analog protein non kolagen.

Metode: Empat kelompok dilakukan demineralisasi buatan. Setelah itu, tiga kelompok dilakukan perendaman dengan larutan remineralisasi yang mengandung asam poliaspartik, sedaangkan satu kelompok tidak dilakukan perendaman larutan remineralisasi asam poliaspartik. Evaluasi remineralisasi dengan Micro-CT.

Hasil: Terlihat remineralisasi pada permukaan demineralized dentin yang ditandai dengan penurunan kedalaman lesi demineralized dentin yang ditandai dengan peningkatan grey scale index setelah dilakukan perendaman dengan larutan remineralisasi asam poliaspartik. Perbandingan rerata empat kelompok menunjukkan perbedaan bermakna.

Kesimpulan: Asam poliaspartik memiliki potensi untuk meremineralisasi demineralized dentin.

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Background: Caries treatment with minimal intervention, namely by removing infected dentine, and leaving affected dentine, then remineralization of affected dentine. In the affected dentine there are still have collagen cross bonds. Dentin remineralization is more complex because there is no residual mineral crystals in dentinal caries. For extrafibrillary and intrafibrillary remineralization in dentine, dentin matrix protein 1 (DMP 1) is a non-collagen protein. The polymer-induced liquid precursor (PILP) process is a Guided Tissue Remineralization method which aims to remineralize intrafibrilar and extafibrilar dentine by adding polymers as analogous to DMP1. One of the non collagen protein analog material is polyacpartic acid.

Objective: To evaluate remineralization of dentine on the demineralized dentin surface after immersion with remineralization solutions containing polyacpartic acid as a non-collagen protein analog.

Method: Four groups carried out artificial demineralization. After that, three groups were immersed with remineralization solution containing polypartic acid, while one group was not immersed in polyacpartic acid remineralization solution. Remineralization evaluation with Micro-CT.

Results: It appears remineralization on the demineralized dentin surface which is characterized by a decrease in the depth of demineralized dentin lesions which is characterized by an increase in gray scale index after immersion with polyacpartic acid remineralization solution. The comparison of the mean of the four groups showed significant differences.

Conclusion: Polyacpartic acid has the potential to remineralize for demineralized dentine.

 

 

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"Latar Belakang: Salah satu material remineralisasi yang banyak digunakan adalah semen ionomer kaca (SIK). Namun dentin terdemineralisasi sesudah aplikasi SIK memiliki sifat mekanis yang berbeda dan lebih rendah daripada dentin normal karena remineralisasi yang terjadi adalah remineralisasi interfibril. Material carboxymethyl chitosan (CMC) bertindak sebagai analog protein nonkolagen yang mampu menstabilisasi nanocluster amorphous calcium phosphate (ACP) dalam proses remineralisasi intrafibril. Tujuan: Mengetahui pengaruh aplikasi modifikasi SIK-CMC5% dan SIK-CMC10% pada dentin terdemineralisasi terhadap kekerasan mikro, fasa mineral dan derajat kristalinitas dentin. Metode: Material SIK dilakukan pencampuran dengan CMC pada rasio 5% dan 10% menghasilkan SIK-CMC5% dan SIK-CMC10%. Kemudian, demineralisasi pada kavitas dentin terdemineralisasi dilakukan dengan aplikasi material SIK, SIK-CMC5% dan SIK-CMC10%. Akar gigi direndam dalam cairan phosphate-buffered saline selama 14 hari. Remineralisasi dentin dievaluasi dari kekerasan mikro melalui uji Vickers dan penilaian fasa mineral dan derajat kristalinitas dentin dari uji X-Ray Diffraction (XRD). Hasil: Kekerasan mikro dentin pada kelompok SIK-CMC5% dan SIK-CMC10% meningkat dibandingkan pada kelompok SIK. Pembentukan kristal hidroksiapatit ditemukan pada sampel SIK dan SIK-CMC, dengan derajat kristalinitas tertinggi pada sampel SIK-CMC10%. Kesimpulan: Semen Ionomer Kaca modifikasi Carboxymethyl Chitosan 10% lebih efektif dalam meningkatkan nilai kekerasan mikro dan mempengaruhi pembentukan fasa mineral kristal hidroksiapatit dan derajat kristalinitas.

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Background: One of the widely used remineralization materials is glass ionomer cement (GIC). However, demineralized dentine after GIC application has different and lower mechanical properties than normal dentin because the remineralization that occurs is interfibril remineralization. Carboxymethyl chitosan (CMC) acts as noncollagenous protein analog that can stabilize amorphous calcium phosphate (ACP) nanoclusters in intrafibril remineralization. Objective: To determine the effect of the application of modified GIC-CMC5% and GIC-CMC10% on the microhardness, mineral phase and degree of crystallinity of demineralized dentin. Methods: GIC material was mixed with CMC at ratio 5% and 10% to produce GIC-CMC5% and GIC-CMC10%. Remineralization of demineralized dentin cavity was carried out by applying GIC, GIC-CMC5% and GIC-CMC10% for 14 days. Remineralization was evaluated from microhardness value through Vickers test and assessment of mineral phase and degree of dentin crystallinity from X-Ray Diffraction (XRD) test. Results: Dentin microhardness in the GIC-CMC5% and GIC-CMC10% was increasing compared to the CIC group. The formation of hydroxyapatite crystals was found in the GIC and GIC-CMC samples with the highest degree of crystallinity in the GIC-CMC10% sample. Conclusion: Modified Glass Ionomer Cement with 10% Carboxymethyl Chitosan is more effective in increasing the microhardness value and affecting the formation of the hydroxyapatite crystalline mineral phase and the degree of crystallinity."