Impact of base type on diclofenac sodium release
from semi-solid dosage forms
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Anna Banyś, Beata Sarecka-Hujar, Andrzej Jankowski, Monika Zalewska
ABSTRACT
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Zakład Technologii Postaci Leku Katedry Farmacji Stosowanej Wydziału Farmaceutycznego z Oddziałem Medycyny Laboratoryjnej Śląskiego Uniwersytetu Medycznego w Katowicach
A D D R E S S F OR C O R R E S P ON DE N C E : Dr n. farm. Anna Banyś
Katedra Farmacji Stosowanej, Zakład Technologii Postaci Leku Wydział Farmaceutyczny
z Oddziałem Medycyny Laboratoryjnej Śląskiego Uniwersytetu Medycznego w Katowicach
ul. Kasztanowa 3 41-200 Sosnowiec tel.: +48 32 269 98 20 e-mail: abanys@sum.edu.pl
Ann. Acad. Med. Siles. 2014, 68, 1, 1–8 Copyright © Śląski Uniwersytet Medyczny w Katowicach
eISSN 1734-025X www.annales.sum.edu.pl
C O N C L U S IO N S
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INTRODUCTION
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Aim of the study
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Fig. 1. Diclofenac sodium release kinetics at 37°C.
Ryc. 1. Kinetyka uwalniania diklofenaku sodu w temperaturze 37°C.
Fig. 2. Comparison of diclofenac sodium amounts released from all analyzed preparations at 32°C and 37°C within 3 hours.
Ryc. 2. Porównanie ilości uwolnionego diklofenaku sodu z wszystkich analizowanych preparatów w temperaturze 32°C i 37°C w czasie 3 godzin.
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Table I. Velocity release constant values k and release half-time t1/2 according to primary kinetics
Tabela I. Wartości stałych szybkości uwalniania k oraz czasu połowicz-nego uwalniania t1/2, dla badanych preparatów według kinetyki I rzędu
Preparations k [h-1] t1/2 [h] 32°C 37°C 32°C 37°C Veral 2.37 x 10-2 3.99 x 10-2 29.24 17.39 Diclac Lipogel 1.90 x 10-2 1.94 x 10-2 36.57 35.74 Gel-type prepara-tion (glycerol ointment) 4.90 x 10 -2 7.00 x 10-2 14.14 9.91 Lipophilic prepara-tion (Vaseline) – 7.29 x 10-4 – 951.09 Absorption prepara-tion (Eucerine) – 4.68 x 10-4 – 1481.86 Emulsion prepara-tion (Lekobaza) 2.36 x 10-3 2.53 x 10-3 293.22 273.47 Emulsion prepara-tion (Hascobaza) 2.55 x 10-3 2.69 x 10-3 272.06 258.10
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