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Hasil Pencarian

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Atria Mya Kelani
Abstrak :
Latar Belakang: Affected dentin merupakan lapisan yang ditinggalkan pada perawatan karies secara minimal invasif karena dapat diremineralisasi. Lapisan ini masih terdapat ikatan silang kolagen yang intak meskipun, mineral apatit telah hilang. Remineralisasi dentin diregulasi oleh protein non kolagen Dentin Matriks Protein 1 (DMP1). Remineralisasi yang dihasilkan berupa remineralisasi intrafibrilar dan ekstrafibrilar. Remineralisasi intrafibrilar meningkatkan sifat fisik dentin. Guided Tissue Remineralization (GTR) merupakan metode remineralisasi dentin secara intrafibrilar dan ekstrafibrilar menggunakan material analog protein non kolagen. Material ini memiliki fungsi menyerupai DMP1. Salah satu material analog protein non kolagen adalah Carboxymethyl Chitosan/ Amorphous Calcium Phosphate (CMC/ACP). Tujuan:  Mengevaluasi remineralisasi dentin pada permukaan demineralized dentin setelah aplikasi material analog protein non kolagen CMC/ACP. Metode: Dua kelompok dilakukan demineralisasi buatan, salah satunya diaplikasikan material CMC/ACP sedangkan, kelompok lainnya tidak diaplikasikan CMC/ACP. Evaluasi remineralisasi dengan SEM dan EDX. Hasil: Terlihat remineralisasi pada permukaan demineralized dentin dan peningkatan kadar kalsium dan fosfat setelah aplikasi CMC/ACP pada hari ke-7. Perbandingan rerata dua kelompok tidak menunjukkan perbedaan bermakna. Kesimpulan: CMC/ACP memiliki potensi untuk meremineralisasi demineralized dentin. ...... Background: Affected dentin is a layer has been left during non invasive caries treatment as it can be remineralized. Collagen crosslinking remains intact in this layer, however the apatite minerals have been lost. Dentin remineralization is regulated by a non collagenous protein, Dentin Matrix Protein 1 (DMP1) and resulting intra- and extrafibrillar remineralization. Intrafibrillar remineralization improves physical properties of dentin. Guided Tissue Remineralization (GTR) is a method of collagen dentin remineralization using non collagen protein analog, resulting in intra- and extrafibrillar remineralization.  This material has similar function with DMP1. Carboxymethyl Chitosan/ Amorphous Calcium Phosphate (CMC/ACP) is one of non collagen protein analog.Aim: To evaluate demineralized dentin remineralization after application non collagen protein analog CMC/ACP. Method: Two groups performed artificial demineralization, one of which applied CMC / ACP material whereas, the other group was not applied CMC / ACP. Remineralization was evalutated using SEM and EDX. Result: After 7 days CMC/ACP application, remineralization was observed on the surface of demineralized dentin, which showed a white irregularities surrounding the dentin tubuli. In addition, increasing calcium and phosphate level has been showed experimentally although, the comparison of both group is insignificant. Conclusion: CMC/ACP has a potential for demineralized dentin remineralization.
Jakarta: Fakultas Kedokteran Gigi Universitas Indonesia, 2018
T-pdf
UI - Tesis Membership  Universitas Indonesia Library
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Febriet Eksadhi Putra
Abstrak :
Telah dilakukan penelitian pengaruh bahan pengisi terhadap pelepasan furosemida dalam sediaan tablet. Tablet dibuat menggunakan metode granulasi basah dengan bahan pengikat larutan karboksimetil kitosan 5% dan bahan pengisi yang berbeda yaitu laktosa (formula A), avicel 101 (formula B), amilum jagung (formula C) dan dikalsium fosfat (formula D). Pelepasan furosemida dari masing-masing tablet dievaluasi menggunakan alat disolusi tipe 2 dengan medium dapar fosfat pH 5,8. Sampel dianalisis menggunakan spektrofotometer pada גּ 274 nm. Hasil penelitian menunjukkan pelepasan furosemida terbesar yaitu 97,91% dihasilkan oleh formula A, kemudian diikuti oleh formula C 97,56%, formula B 78,56% dan formula D 35,82%.
It is been done experiment toward the influence of filler toward the releasing of furosemida from the tablet dosage form. The tablet is made by using the wet granulation method with carboxymethyl chitosan solution as the binding agent and different filler lactose (formula A), avicel 101 (formula B), corn starch (formula C) and dicalsium fosfat (formula D). The releasing of furosemida from tablet is evaluated by using the disolution apparatus type 2 with buffer fosfat pH 5,8 as medium. The sample is analyzed by using the spektrofotometer on the גּ 274 nm. The results showed the releasing of furosemida of formula A (97,91%), formula C (97,17%), formula B (78,56%) and formula D (35,82%).
Depok: Fakultas Farmasi Universitas Indonesia, 2006
S32854
UI - Skripsi Membership  Universitas Indonesia Library