FORMULASI SEDIAAN KRIM TRANSFERSOM KAFEIN DAN UJI DIFUSI SEDIAAN SECARA IN VITRO

Cellulite is topographic skin change caused by localized metabolic disorder on subcutaneous tissue with high prevalency in women. Caffeine used to treat cellulite has lipolytic activity on fatty cells. This study aims to develop the formulation to enhance caffeine skin penetration through elastic...

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Main Author: Zakkaha, Ziyani
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/45404
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:45404
spelling id-itb.:454042019-12-18T14:07:46ZFORMULASI SEDIAAN KRIM TRANSFERSOM KAFEIN DAN UJI DIFUSI SEDIAAN SECARA IN VITRO Zakkaha, Ziyani Indonesia Final Project - INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/45404 Cellulite is topographic skin change caused by localized metabolic disorder on subcutaneous tissue with high prevalency in women. Caffeine used to treat cellulite has lipolytic activity on fatty cells. This study aims to develop the formulation to enhance caffeine skin penetration through elastic and ultradeformable (transfersome) vesicle delivery system. Transfersomes consisted of Lecithin S-100 and sorbitan monooleate were prepared by thin film hydration method. The first step was dissolving each component in chloroform and evaporated using rotary evaporator until dry. The thin film was kept in a vacuum overnight and hydrated with phosphate buffer pH 7,4 by rotation using rotary evaporator to form vesicle suspension. After that, the vesicle suspension was sonicated using probe sonicator and extruded through filter membrane 0,2 µm. Furthermore, formulation of transfersome was done by phospholipid and surfactant in ratio 49:1, 87:13, and 4:1 (%w/w). The transfersome of this characterized by determination vesicle size, polydispersity index, entrapment efficiency, deformability, and in vitro diffusion test using Franz cell. The optimum formula for caffeine-loaded transfersome consisted of Lecithin S-100 as phospholipid and sorbitan monooleate in ratio 49:1 (%w/w) and caffeine 0,2%. After optimizing this formula, the result of average particle size of transfersome caffeine was 188,9±4,4 nm with polydispersity index 0,339±0,069 and entrapment efficiency 97,65±0,64%. The difference diffusion test between caffeine-loaded transfersome, caffeine cream, and caffeine-loaded transfersome in cream that could diffuse through membrane were 79,22±0,89%, 20,61±2,76%, and 4,69±0,71%. Caffeine-loaded transfersome in cream significantly enhanced the penetration of membrane shed snake skin compared to the caffeine cream without transfersome (P<0,05). 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 Cellulite is topographic skin change caused by localized metabolic disorder on subcutaneous tissue with high prevalency in women. Caffeine used to treat cellulite has lipolytic activity on fatty cells. This study aims to develop the formulation to enhance caffeine skin penetration through elastic and ultradeformable (transfersome) vesicle delivery system. Transfersomes consisted of Lecithin S-100 and sorbitan monooleate were prepared by thin film hydration method. The first step was dissolving each component in chloroform and evaporated using rotary evaporator until dry. The thin film was kept in a vacuum overnight and hydrated with phosphate buffer pH 7,4 by rotation using rotary evaporator to form vesicle suspension. After that, the vesicle suspension was sonicated using probe sonicator and extruded through filter membrane 0,2 µm. Furthermore, formulation of transfersome was done by phospholipid and surfactant in ratio 49:1, 87:13, and 4:1 (%w/w). The transfersome of this characterized by determination vesicle size, polydispersity index, entrapment efficiency, deformability, and in vitro diffusion test using Franz cell. The optimum formula for caffeine-loaded transfersome consisted of Lecithin S-100 as phospholipid and sorbitan monooleate in ratio 49:1 (%w/w) and caffeine 0,2%. After optimizing this formula, the result of average particle size of transfersome caffeine was 188,9±4,4 nm with polydispersity index 0,339±0,069 and entrapment efficiency 97,65±0,64%. The difference diffusion test between caffeine-loaded transfersome, caffeine cream, and caffeine-loaded transfersome in cream that could diffuse through membrane were 79,22±0,89%, 20,61±2,76%, and 4,69±0,71%. Caffeine-loaded transfersome in cream significantly enhanced the penetration of membrane shed snake skin compared to the caffeine cream without transfersome (P<0,05).
format Final Project
author Zakkaha, Ziyani
spellingShingle Zakkaha, Ziyani
FORMULASI SEDIAAN KRIM TRANSFERSOM KAFEIN DAN UJI DIFUSI SEDIAAN SECARA IN VITRO
author_facet Zakkaha, Ziyani
author_sort Zakkaha, Ziyani
title FORMULASI SEDIAAN KRIM TRANSFERSOM KAFEIN DAN UJI DIFUSI SEDIAAN SECARA IN VITRO
title_short FORMULASI SEDIAAN KRIM TRANSFERSOM KAFEIN DAN UJI DIFUSI SEDIAAN SECARA IN VITRO
title_full FORMULASI SEDIAAN KRIM TRANSFERSOM KAFEIN DAN UJI DIFUSI SEDIAAN SECARA IN VITRO
title_fullStr FORMULASI SEDIAAN KRIM TRANSFERSOM KAFEIN DAN UJI DIFUSI SEDIAAN SECARA IN VITRO
title_full_unstemmed FORMULASI SEDIAAN KRIM TRANSFERSOM KAFEIN DAN UJI DIFUSI SEDIAAN SECARA IN VITRO
title_sort formulasi sediaan krim transfersom kafein dan uji difusi sediaan secara in vitro
url https://digilib.itb.ac.id/gdl/view/45404
_version_ 1822927085423820800