New formulation of in situ gelling Metolose-based liquid suppository

Context: An in situ gelling liquid suppository is liquid at room temperature but forms a gel at body temperature. In our work, Metolose® SM-4000 (methylcellulose) is studied that basically shows thermal gelation at 68°C (2%, w w). Objective: The objective was to study the potency of different factor...

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Veröffentlicht in:Drug development and industrial pharmacy 2011-01, Vol.37 (1), p.1-7
Hauptverfasser: Pásztor, E., Makó, Á., Csóka, G., Fenyvesi, Zs, Benko, R., Prosszer, M., Marton, S., Antal, I., Klebovich, I.
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container_end_page 7
container_issue 1
container_start_page 1
container_title Drug development and industrial pharmacy
container_volume 37
creator Pásztor, E.
Makó, Á.
Csóka, G.
Fenyvesi, Zs
Benko, R.
Prosszer, M.
Marton, S.
Antal, I.
Klebovich, I.
description Context: An in situ gelling liquid suppository is liquid at room temperature but forms a gel at body temperature. In our work, Metolose® SM-4000 (methylcellulose) is studied that basically shows thermal gelation at 68°C (2%, w w). Objective: The objective was to study the potency of different factors (concentration, pH, additives) to change the value of thermal gelation temperature (T t) for Metolose® to form an in situ gelling liquid suppository. Materials and methods: We studied the effect of Metolose® concentration, pH, and salts (sodium chloride, potassium chloride, sodium hydrogen carbonate, and sodium monohydrogen phosphate) on T t by viscosimetry. To choose the appropriate compound, in vitro drug release was examined. Rectal safety test was performed on rats in vivo after 12-hour application. Results: Increasing the Metolose® concentrations (0.5-4%, w w), T t can be decreased, but it also altered the consistency of gel. pH does not affect the T t. The water-soluble salts allowed reducing the gelation temperature to 37°C. Sodium monohydrogen phosphate in 4.5% concentration was found to be the most appropriate. The impact of examined factors on in vitro drug release of piroxicam from the in situ-formed gel was characterized according to Fickian diffusion. Metolose® and the chosen salt did not cause any morphological damage on the rectal tissues. Discussion: According to our study, Metolose® has the physical and chemical potential to be used as base for liquid suppositories.
doi_str_mv 10.3109/03639045.2010.489558
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In our work, Metolose® SM-4000 (methylcellulose) is studied that basically shows thermal gelation at 68°C (2%, w w). Objective: The objective was to study the potency of different factors (concentration, pH, additives) to change the value of thermal gelation temperature (T t) for Metolose® to form an in situ gelling liquid suppository. Materials and methods: We studied the effect of Metolose® concentration, pH, and salts (sodium chloride, potassium chloride, sodium hydrogen carbonate, and sodium monohydrogen phosphate) on T t by viscosimetry. To choose the appropriate compound, in vitro drug release was examined. Rectal safety test was performed on rats in vivo after 12-hour application. Results: Increasing the Metolose® concentrations (0.5-4%, w w), T t can be decreased, but it also altered the consistency of gel. pH does not affect the T t. The water-soluble salts allowed reducing the gelation temperature to 37°C. Sodium monohydrogen phosphate in 4.5% concentration was found to be the most appropriate. The impact of examined factors on in vitro drug release of piroxicam from the in situ-formed gel was characterized according to Fickian diffusion. Metolose® and the chosen salt did not cause any morphological damage on the rectal tissues. 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Sodium monohydrogen phosphate in 4.5% concentration was found to be the most appropriate. The impact of examined factors on in vitro drug release of piroxicam from the in situ-formed gel was characterized according to Fickian diffusion. Metolose® and the chosen salt did not cause any morphological damage on the rectal tissues. 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subjects Administration, Rectal
Animals
Anti-Inflammatory Agents, Non-Steroidal - administration & dosage
Anti-Inflammatory Agents, Non-Steroidal - chemistry
Chemistry, Pharmaceutical - methods
Gels - chemistry
Hydrogen-Ion Concentration
In situ gelling suppository
Male
Methylcellulose - chemistry
Metolose
Models, Biological
Phosphates - chemistry
piroxicam
Piroxicam - administration & dosage
Piroxicam - chemistry
Rats
Rats, Wistar
Suppositories - chemistry
Temperature
title New formulation of in situ gelling Metolose-based liquid suppository
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