FORMULASI DAN EVALUASI NANOSTRUCTURED LIPID CARRIERS (NLC) SULFASALAZIN YANG BERPOTENSI UNTUK PENGGUNAAN RUTE TRANSDERMAL

Application of oral sulfasalazine provides a bioavailability less than 15% and side effect on mouth such as mouth ulcer and on the gastrointestinal tract such as nausea, diarrhea, dyspepsia, abdominal pain, and stomatitis. Transdermal dosage form is used to overcome this problem. Stratum corneum...

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Main Author: Pinta Anugrah, Threefanny
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/44290
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:44290
spelling id-itb.:442902019-10-07T16:00:05ZFORMULASI DAN EVALUASI NANOSTRUCTURED LIPID CARRIERS (NLC) SULFASALAZIN YANG BERPOTENSI UNTUK PENGGUNAAN RUTE TRANSDERMAL Pinta Anugrah, Threefanny Indonesia Final Project Sulfasalazine, Nano Lipid Carriers (NLC), transdermal, in vitro difussion INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/44290 Application of oral sulfasalazine provides a bioavailability less than 15% and side effect on mouth such as mouth ulcer and on the gastrointestinal tract such as nausea, diarrhea, dyspepsia, abdominal pain, and stomatitis. Transdermal dosage form is used to overcome this problem. Stratum corneum acts as barrier for penetration sulfasalazine pass through the skin. In a previous study SLN has been developed to improve sulfasalazine penetration through the stratum corneum, but the SLN provided bad physical stability. The NLC formula is developed to improved the physicochemical properties of SLN. NLC was prepared by combination of high speed homogenization with sonication method. NLC formulation optimum consist of lipid (8% w/v) with 90:10 apifil-oleic acid ratio, 8% of plantacare, and 1% of sulfasalazine. Characterization study was accomplished to particle size measurement, polydispersity index, potential zeta measurement, entrapment efficiency, physical stability and in vitro diffusion test. Particle size of obtained NLC was 284,3 nm with polydispersity index of 0,318 and potential zeta value of -33,11 mV. Entrapment efficiency sulfasalazine in NLC was 71,9%. Morphology by TEM revealed near spherical shape of NLC. NLC physical stability by freeze and thaw for 3 cycles and storage at 4 °C and 40 °C showed better stability of particle size than storage at 25 °C. In vitro diffusion test show that flux sulfasalazine with 124 × 10 -3 mg/cm 2 /hr was improved compared to SLN sulfasalazine. Flux sulfasalazine NLC loading gel was 10,1 × 10-3 mg/cm 2 /hr was preferable compared to sulfasalazine suspension with flux of 4,105 × 10 -3 mg/cm 2 /hr. NLC sulfasalazine provides better physicochemical properties in comparison of with SLN sulfasalazin. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description Application of oral sulfasalazine provides a bioavailability less than 15% and side effect on mouth such as mouth ulcer and on the gastrointestinal tract such as nausea, diarrhea, dyspepsia, abdominal pain, and stomatitis. Transdermal dosage form is used to overcome this problem. Stratum corneum acts as barrier for penetration sulfasalazine pass through the skin. In a previous study SLN has been developed to improve sulfasalazine penetration through the stratum corneum, but the SLN provided bad physical stability. The NLC formula is developed to improved the physicochemical properties of SLN. NLC was prepared by combination of high speed homogenization with sonication method. NLC formulation optimum consist of lipid (8% w/v) with 90:10 apifil-oleic acid ratio, 8% of plantacare, and 1% of sulfasalazine. Characterization study was accomplished to particle size measurement, polydispersity index, potential zeta measurement, entrapment efficiency, physical stability and in vitro diffusion test. Particle size of obtained NLC was 284,3 nm with polydispersity index of 0,318 and potential zeta value of -33,11 mV. Entrapment efficiency sulfasalazine in NLC was 71,9%. Morphology by TEM revealed near spherical shape of NLC. NLC physical stability by freeze and thaw for 3 cycles and storage at 4 °C and 40 °C showed better stability of particle size than storage at 25 °C. In vitro diffusion test show that flux sulfasalazine with 124 × 10 -3 mg/cm 2 /hr was improved compared to SLN sulfasalazine. Flux sulfasalazine NLC loading gel was 10,1 × 10-3 mg/cm 2 /hr was preferable compared to sulfasalazine suspension with flux of 4,105 × 10 -3 mg/cm 2 /hr. NLC sulfasalazine provides better physicochemical properties in comparison of with SLN sulfasalazin.
format Final Project
author Pinta Anugrah, Threefanny
spellingShingle Pinta Anugrah, Threefanny
FORMULASI DAN EVALUASI NANOSTRUCTURED LIPID CARRIERS (NLC) SULFASALAZIN YANG BERPOTENSI UNTUK PENGGUNAAN RUTE TRANSDERMAL
author_facet Pinta Anugrah, Threefanny
author_sort Pinta Anugrah, Threefanny
title FORMULASI DAN EVALUASI NANOSTRUCTURED LIPID CARRIERS (NLC) SULFASALAZIN YANG BERPOTENSI UNTUK PENGGUNAAN RUTE TRANSDERMAL
title_short FORMULASI DAN EVALUASI NANOSTRUCTURED LIPID CARRIERS (NLC) SULFASALAZIN YANG BERPOTENSI UNTUK PENGGUNAAN RUTE TRANSDERMAL
title_full FORMULASI DAN EVALUASI NANOSTRUCTURED LIPID CARRIERS (NLC) SULFASALAZIN YANG BERPOTENSI UNTUK PENGGUNAAN RUTE TRANSDERMAL
title_fullStr FORMULASI DAN EVALUASI NANOSTRUCTURED LIPID CARRIERS (NLC) SULFASALAZIN YANG BERPOTENSI UNTUK PENGGUNAAN RUTE TRANSDERMAL
title_full_unstemmed FORMULASI DAN EVALUASI NANOSTRUCTURED LIPID CARRIERS (NLC) SULFASALAZIN YANG BERPOTENSI UNTUK PENGGUNAAN RUTE TRANSDERMAL
title_sort formulasi dan evaluasi nanostructured lipid carriers (nlc) sulfasalazin yang berpotensi untuk penggunaan rute transdermal
url https://digilib.itb.ac.id/gdl/view/44290
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