Abstract :
(ABSTRAKSI) Prometazin HCl mengalami efek lintas pertama hepatik sehingga memiliki
bioavilabilitas yang relatif rendah yaitu sekitar 25%. Absorbsi oral sering
terganggu oleh mual dan muntah, sehingga bioavilabilitas obat semakin rendah dan morning sickness tidak terterapi dengan baik. Penelitian ini bertujuan untuk
mengetahui : 1) pengaruh variasi kadar propilen glikol, Tween 80 dan intensitas
arus iontoforesis beserta interaksinya terhadap transpor prometazin HCl, 2)
menentukan komposisi teoritis formula optimal prometazin HCl dalam sediaan transdermal secara in vitro.
Enhancer propilen glikol, Tween 80 dan intensitas arus iontoforesis
digunakan sebagai faktor dalam factorial design 23 dengan menggunakan delapan kondisi uji. Efek peningkat penetrasi terhadap transpor prometazin HCl diuji
secara in vitro menggunakan sel difusi franz cell like tipe vertikal. Kulit tikus
yang digunakan sebagai membran mengalami praperlakuan dengan propilen glikol dan Tween 80 kemudian dilakukan iontoforesis. Prometazin HCl yang tertranspor melalui membran kulit tikus galur wistar diukur dengan metode spektrofotometri pada ëmax 251 nm. Analisis data menggunakan modeling
WinSAAM berbasis kompartemen digunakan untuk mengetahui mekanisme
transpor dan pengaruh enhancer. Optimasi dilakukan dengan metode factorial design menggunakan software Design Expert® 7.1.4. Transpor prometazin HCl dapat dijelaskan dengan model empat kompartemen. Peningkatan konsentrai propilen glikol dan intensitas arus
iontoforesis secara signifikan meningkatkan nilai Cp maks, AUC dan AD. Secara teoritis interaksi propilen glikol-iontoforesis secara signifikan meningkatkan nilai
Cp maks, AUC dan AD. Peningkatan konsentrasi Tween 80, interaksi Tween 80-
propilen glikol serta Tween 80-iontoforesis secara signifikan menurunkan nilai Cp maks, AUC dan AD. Berdasarkan harga parameter Cp maks, AUC dan AD
komposisi kondisi uji optimal adalah propilen glikol 20%, Tween 1% dan iontoforesis 0,5 mA/cm2. Secara teoritis kondisi tersebut menghasilkan harga Cp
maks 775,519 ng/L, AUC 121 ,073 ìg dan AD 165,686 ìg. (ABSTRACT) Promethazine HCl undergoes extensive hepatic first-pass metabolism
following oral administration resulted in a low bioavailability at around 25%. Oral
absorption is often interrupted by nausea and vomiting, so the bioavalability is
low and morning sickness is not treated verry well. The purposes of this study were to evaluate the : 1) influence of propylene glycol, Tween 80 concentrations
as enhancer and iontophoretic current density on the transport of promehtazine
HCl, 2) to determine theoretical composition of optimum condition transdermal delivery system of promethazine HCl in transdermal preparation in vitro. Eight condition were prepared according to 23 factorial design employing
propylene glycol, Tween 80 and iontophoretic current density. Ehancement effect on transport of prometazin HCl was investigated across hairless rat skin as
membrane. The study was carried out by using vertical diffusion cell (franz cell
like). Transport of promehtazine HCl across membrane was determined spectrophotometrically at ëmax 251 nm. Data were analysed based on WinSAAM compartement modeling to determine transport kinetics and the effects of
enhancers. Optimization was conducted by factorial design using Design Expert ®
7.1.4 software.
Increasing propylene glycol concentration and the current of iontophoretic
significantly increased the Cp max, AUC and also the potential of the drug to
difuse (AD). Increasing Tween 80 concentration significantly decrease the Cp
max, AUC and also AD. Interactions of propylene glycol and iontophoretic
current density significantly increase Cp max, AUC and AD. Interaction of Tween 80 and propylene glycol and also interaction of Tween 80 and iontophoretic
current density significantly decrease Cp max, AUC and AD. Based on values of
Cp max, AUC and AD optimum composition of the condition containing
propylene glycol, Tween 80 and iontophoretic current density which have the percentage and current density of 20%, 1% and 0,5 mA/cm2, respectively. Theoritically, this composition has Cp max, AUC and AD value of 775,519 ng/L, 121 ,073 ìg and 165,686 ìg.