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Skin premature aging is characterized by fine wrinkles and decreased elasticity. It can be <br /> <br /> <br /> <br /> overcome by stimulating collagen production and inhibiting its degradation, and also reducing <br /> <br /> <br /> <br /> cor...
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id-itb.:287242018-07-02T13:04:15Z#TITLE_ALTERNATIVE# PRIHANTINI NIM: 20715021, MALINDA Indonesia Theses INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/28724 Skin premature aging is characterized by fine wrinkles and decreased elasticity. It can be <br /> <br /> <br /> <br /> overcome by stimulating collagen production and inhibiting its degradation, and also reducing <br /> <br /> <br /> <br /> corneocyte buildup. Madeira vein play a role in solving the problem, which has been shown to <br /> <br /> <br /> <br /> induce collagen production and inhibit its degradation. The aim of this research was to optimize <br /> <br /> <br /> <br /> W/O/W multiple nanoemulsion formula of Madeira vein-leaves extract in the W1 phase and <br /> <br /> <br /> <br /> glycolic acid in the W2 phase. Crude drug was extracted using 96% ethanol, concentrated using <br /> <br /> <br /> <br /> rotavapor then the extract was determined the weight density and total flavonoid. Glycolic acid <br /> <br /> <br /> <br /> was added after conjugated with chitosan to reduce its stinging effect on the skin. The W/O/W <br /> <br /> <br /> <br /> multiple nanoemulsion was prepared through two emulsification steps: W1/O primary emulsion <br /> <br /> <br /> <br /> using homogenizer at 10,000 rpm for 10 min, and the secondary emulsion using magnetic stirrer <br /> <br /> <br /> <br /> at 550 rpm. Primary emulsion was optimized including the selection of cosurfactant and extract <br /> <br /> <br /> <br /> concentration, followed by secondary emulsion optimization using response surface methodology <br /> <br /> <br /> <br /> consisted of 2-level factorial 1/4 full and Box-Behnken design. The 1% extract showed 0.93 g/mL <br /> <br /> <br /> <br /> weight density and 2.47% total flavonoid. The W1/O primary emulsion consisted of 5% extract, <br /> <br /> <br /> <br /> 10% aquadeion, 27.5% polisorbat 80 as surfactant, 12.5% PEG 400 as cosurfactant, and 45% <br /> <br /> <br /> <br /> isopropyl myristate as oil phase. The 2-level factorial 1/4 full gave the three significant factors: <br /> <br /> <br /> <br /> W1/O sonication time, W1/O concentration, and secondary emulsification stirring time. Box- <br /> <br /> <br /> <br /> Behnken optimization for globule size below 400 nm was obtained by 6-10 minutes W1/O <br /> <br /> <br /> <br /> sonication time, 12-16% W1/O concentration, and 32-42 minutes stirring time of secondary <br /> <br /> <br /> <br /> emulsion. <br /> <br /> text |
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Skin premature aging is characterized by fine wrinkles and decreased elasticity. It can be <br />
<br />
<br />
<br />
overcome by stimulating collagen production and inhibiting its degradation, and also reducing <br />
<br />
<br />
<br />
corneocyte buildup. Madeira vein play a role in solving the problem, which has been shown to <br />
<br />
<br />
<br />
induce collagen production and inhibit its degradation. The aim of this research was to optimize <br />
<br />
<br />
<br />
W/O/W multiple nanoemulsion formula of Madeira vein-leaves extract in the W1 phase and <br />
<br />
<br />
<br />
glycolic acid in the W2 phase. Crude drug was extracted using 96% ethanol, concentrated using <br />
<br />
<br />
<br />
rotavapor then the extract was determined the weight density and total flavonoid. Glycolic acid <br />
<br />
<br />
<br />
was added after conjugated with chitosan to reduce its stinging effect on the skin. The W/O/W <br />
<br />
<br />
<br />
multiple nanoemulsion was prepared through two emulsification steps: W1/O primary emulsion <br />
<br />
<br />
<br />
using homogenizer at 10,000 rpm for 10 min, and the secondary emulsion using magnetic stirrer <br />
<br />
<br />
<br />
at 550 rpm. Primary emulsion was optimized including the selection of cosurfactant and extract <br />
<br />
<br />
<br />
concentration, followed by secondary emulsion optimization using response surface methodology <br />
<br />
<br />
<br />
consisted of 2-level factorial 1/4 full and Box-Behnken design. The 1% extract showed 0.93 g/mL <br />
<br />
<br />
<br />
weight density and 2.47% total flavonoid. The W1/O primary emulsion consisted of 5% extract, <br />
<br />
<br />
<br />
10% aquadeion, 27.5% polisorbat 80 as surfactant, 12.5% PEG 400 as cosurfactant, and 45% <br />
<br />
<br />
<br />
isopropyl myristate as oil phase. The 2-level factorial 1/4 full gave the three significant factors: <br />
<br />
<br />
<br />
W1/O sonication time, W1/O concentration, and secondary emulsification stirring time. Box- <br />
<br />
<br />
<br />
Behnken optimization for globule size below 400 nm was obtained by 6-10 minutes W1/O <br />
<br />
<br />
<br />
sonication time, 12-16% W1/O concentration, and 32-42 minutes stirring time of secondary <br />
<br />
<br />
<br />
emulsion. <br />
<br />
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PRIHANTINI NIM: 20715021, MALINDA |
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PRIHANTINI NIM: 20715021, MALINDA #TITLE_ALTERNATIVE# |
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PRIHANTINI NIM: 20715021, MALINDA |
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PRIHANTINI NIM: 20715021, MALINDA |
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https://digilib.itb.ac.id/gdl/view/28724 |
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