Department of Pharmaceutics, Semmelweis University, Budapest, Hungary.
Drug Dev Ind Pharm. 2011 Jan;37(1):1-7. doi: 10.3109/03639045.2010.489558. Epub 2010 Aug 12.
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).
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.
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.
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.
According to our study, Metolose® has the physical and chemical potential to be used as base for liquid suppositories.
原位凝胶栓剂在室温下为液态,但在体温下形成凝胶。在我们的工作中,研究了甲基纤维素 Metolose® SM-4000,它基本在 68°C(2%,w/w)下表现出热凝胶化。
本研究旨在探讨不同因素(浓度、pH 值、添加剂)对改变甲基纤维素热凝胶化温度(T(t))的能力,以形成原位凝胶栓剂。
通过黏度法研究了甲基纤维素浓度、pH 值和盐(氯化钠、氯化钾、碳酸氢钠和磷酸氢二钠)对 T(t)的影响。为选择合适的化合物,进行了体外药物释放研究。对大鼠进行了 12 小时直肠给药后的体内直肠安全性试验。
增加甲基纤维素浓度(0.5-4%,w/w)可降低 T(t),但也改变了凝胶的稠度。pH 值不影响 T(t)。水溶性盐可将凝胶化温度降低至 37°C。发现 4.5%浓度的磷酸氢二钠最为合适。根据菲克扩散,考察了各因素对原位形成凝胶中吡罗昔康体外药物释放的影响。甲基纤维素和所选盐对直肠组织没有造成任何形态损伤。
根据我们的研究,甲基纤维素具有作为液体栓剂基质的物理和化学潜力。