The object of this study was to prepare and evaluated a matrix type transdermal patch of meloxicam using blend of polyvinylpyrolidone (PVP K-30) and ethylcellulose (EC N-22) were 1:9 (Formula I); 2:8 (Formula II); and 3:7 (Formula III). Evaluation of patch is organoleptic, percentage moisture content, and the release of the drug. Results were analyzed by statistic programmed of SPSS using one way analysis of variance with degree of believed 95% ( = 0.05). The results of organoleptic evaluation of patch dosage, transdermal patches were found yellow, odorless, and dry. Results test percentage moisture content (Formula I) 1.501 ± 0.022 %; (Formula II) 2.206 ± 0.010 %; dan (Formula III) 3.725 ± 0.033 %. Results test flux (Formula I) 455.078 ± 0...
Abstract: Transdermal delivery system is one of the delivery system for Pentagamavunon-0 (PGV-0) toa...
The transdermal patch can deliver the active substance with good bioavailability, then made formulat...
Meloxicam is an NSAID drug that can cause gastric irritation in oral administration. Transdermal dr...
The present research has been undertaken with the aim to develop a transdermal patch of meloxicam wi...
ABSTRAK Pelepasan natrium diklofenak dari Sediaan Transdermal Patch Tipe Matriks dengan kombi...
ABSTRAK Pelepasan natrium diklofenak dari Sediaan Transdermal Patch Tipe Matriks dengan komb...
oai:ojs2.jtpc.farmasi.unmul.ac.id:article/1The sodium diclofenac realeased from transdermal patch of...
Meloxicam is non steroidal antiinflammatory drug (NSAID) of the enolic acid class which is widely us...
Transdermal drug delivery is controlled release of drugs through the skin to obtain therapeutic lev...
In this study, matrix type transdermal patch containing meloxicam were prepared using three combinat...
Meloxicam is an Nonsteroidal Anti-Inflammatory Drugs or often known as NSAID used in osteoarthritis ...
Abstrak Kalium diklofenak adalah salah satu obat golongan anti-inflamasi non steroid (AINS) yang mem...
The sodium diclofenac realeased from transdermal patch of combination of EC N–20 and PVP K–30 with r...
Pelepasan natrium diklofenak dari Sediaan Transdermal Patch Tipe Matriks dengan kombinasi polimer et...
Telah dilakukan penelitian pelepasan sodium diklofenak dari transdemal Patch kombinasi matriks EC N–...
Abstract: Transdermal delivery system is one of the delivery system for Pentagamavunon-0 (PGV-0) toa...
The transdermal patch can deliver the active substance with good bioavailability, then made formulat...
Meloxicam is an NSAID drug that can cause gastric irritation in oral administration. Transdermal dr...
The present research has been undertaken with the aim to develop a transdermal patch of meloxicam wi...
ABSTRAK Pelepasan natrium diklofenak dari Sediaan Transdermal Patch Tipe Matriks dengan kombi...
ABSTRAK Pelepasan natrium diklofenak dari Sediaan Transdermal Patch Tipe Matriks dengan komb...
oai:ojs2.jtpc.farmasi.unmul.ac.id:article/1The sodium diclofenac realeased from transdermal patch of...
Meloxicam is non steroidal antiinflammatory drug (NSAID) of the enolic acid class which is widely us...
Transdermal drug delivery is controlled release of drugs through the skin to obtain therapeutic lev...
In this study, matrix type transdermal patch containing meloxicam were prepared using three combinat...
Meloxicam is an Nonsteroidal Anti-Inflammatory Drugs or often known as NSAID used in osteoarthritis ...
Abstrak Kalium diklofenak adalah salah satu obat golongan anti-inflamasi non steroid (AINS) yang mem...
The sodium diclofenac realeased from transdermal patch of combination of EC N–20 and PVP K–30 with r...
Pelepasan natrium diklofenak dari Sediaan Transdermal Patch Tipe Matriks dengan kombinasi polimer et...
Telah dilakukan penelitian pelepasan sodium diklofenak dari transdemal Patch kombinasi matriks EC N–...
Abstract: Transdermal delivery system is one of the delivery system for Pentagamavunon-0 (PGV-0) toa...
The transdermal patch can deliver the active substance with good bioavailability, then made formulat...
Meloxicam is an NSAID drug that can cause gastric irritation in oral administration. Transdermal dr...