FORMULASI MATRIKS TRANSDERMAL PENTAGAMAVUNON-0 DENGAN KOMBINASI POLIMER PVP K30 DAN HIDROKSIPROPIL METILSELULOSA
Abstract: Transdermal delivery system is one of the delivery system for Pentagamavunon-0 (PGV-0) to avoid the high intensity of first pass metabolism of PGV-0 in peroral route. The purpose of this research was to optimize the formula of PGV-0 transdermal matrix with a combination of PVP K30 and HPMC...
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Universitas Sanata Dharma
2016-04-01
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Series: | Jurnal Farmasi Sains dan Komunitas |
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doaj-1d0ac1ad22284785ae20fc44d4bc27172020-11-25T01:27:48ZengUniversitas Sanata DharmaJurnal Farmasi Sains dan Komunitas1693-56832527-71462016-04-0111210.24071/jpsc.1129994FORMULASI MATRIKS TRANSDERMAL PENTAGAMAVUNON-0 DENGAN KOMBINASI POLIMER PVP K30 DAN HIDROKSIPROPIL METILSELULOSABeti PudyastutiAkhmad Kharis NugrohoSudibyo MartonoAbstract: Transdermal delivery system is one of the delivery system for Pentagamavunon-0 (PGV-0) to avoid the high intensity of first pass metabolism of PGV-0 in peroral route. The purpose of this research was to optimize the formula of PGV-0 transdermal matrix with a combination of PVP K30 and HPMC polymers.The simplex lattice optimization approach of the transdermal matrix formulas was performed by using Design Expert 7.1.5 software. The visual appearance, weight, thickness, moisture content, moisture uptake, folding endurance, drug content, and dissolution efficiency of the release profil of PGV-0 from the matrix for 6 hours were evaluated as responses to determine optimum formula of matrix. The result showed that a combination of PVP K30 and HPMC polymers had a significant influence on the visual appearance, moisture content, and dissolution efficiency of PGV-0. Combination of 1.98% of PVP K30 and 4.52% of HPMC as the optimum formula could produce homogeneous and flexible matrix with moisture content of 3.21%. The dissolution efficiency was 9.11%, indicating that 101.93 µg of PGV-0 was released from the optimum formula during 6 hours. Keywords : Pentagamavunon-0, Transdermal matrix, PVP K30, HPMChttp://e-journal.usd.ac.id/index.php/JFSK/article/view/99 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Beti Pudyastuti Akhmad Kharis Nugroho Sudibyo Martono |
spellingShingle |
Beti Pudyastuti Akhmad Kharis Nugroho Sudibyo Martono FORMULASI MATRIKS TRANSDERMAL PENTAGAMAVUNON-0 DENGAN KOMBINASI POLIMER PVP K30 DAN HIDROKSIPROPIL METILSELULOSA Jurnal Farmasi Sains dan Komunitas |
author_facet |
Beti Pudyastuti Akhmad Kharis Nugroho Sudibyo Martono |
author_sort |
Beti Pudyastuti |
title |
FORMULASI MATRIKS TRANSDERMAL PENTAGAMAVUNON-0 DENGAN KOMBINASI POLIMER PVP K30 DAN HIDROKSIPROPIL METILSELULOSA |
title_short |
FORMULASI MATRIKS TRANSDERMAL PENTAGAMAVUNON-0 DENGAN KOMBINASI POLIMER PVP K30 DAN HIDROKSIPROPIL METILSELULOSA |
title_full |
FORMULASI MATRIKS TRANSDERMAL PENTAGAMAVUNON-0 DENGAN KOMBINASI POLIMER PVP K30 DAN HIDROKSIPROPIL METILSELULOSA |
title_fullStr |
FORMULASI MATRIKS TRANSDERMAL PENTAGAMAVUNON-0 DENGAN KOMBINASI POLIMER PVP K30 DAN HIDROKSIPROPIL METILSELULOSA |
title_full_unstemmed |
FORMULASI MATRIKS TRANSDERMAL PENTAGAMAVUNON-0 DENGAN KOMBINASI POLIMER PVP K30 DAN HIDROKSIPROPIL METILSELULOSA |
title_sort |
formulasi matriks transdermal pentagamavunon-0 dengan kombinasi polimer pvp k30 dan hidroksipropil metilselulosa |
publisher |
Universitas Sanata Dharma |
series |
Jurnal Farmasi Sains dan Komunitas |
issn |
1693-5683 2527-7146 |
publishDate |
2016-04-01 |
description |
Abstract: Transdermal delivery system is one of the delivery system for Pentagamavunon-0 (PGV-0) to avoid the high intensity of first pass metabolism of PGV-0 in peroral route. The purpose of this research was to optimize the formula of PGV-0 transdermal matrix with a combination of PVP K30 and HPMC polymers.The simplex lattice optimization approach of the transdermal matrix formulas was performed by using Design Expert 7.1.5 software. The visual appearance, weight, thickness, moisture content, moisture uptake, folding endurance, drug content, and dissolution efficiency of the release profil of PGV-0 from the matrix for 6 hours were evaluated as responses to determine optimum formula of matrix. The result showed that a combination of PVP K30 and HPMC polymers had a significant influence on the visual appearance, moisture content, and dissolution efficiency of PGV-0. Combination of 1.98% of PVP K30 and 4.52% of HPMC as the optimum formula could produce homogeneous and flexible matrix with moisture content of 3.21%. The dissolution efficiency was 9.11%, indicating that 101.93 µg of PGV-0 was released from the optimum formula during 6 hours.
Keywords : Pentagamavunon-0, Transdermal matrix, PVP K30, HPMC |
url |
http://e-journal.usd.ac.id/index.php/JFSK/article/view/99 |
work_keys_str_mv |
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