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掩味剂对用于对乙酰氨基酚和氨溴索口服缓释给药的原位凝胶化果胶制剂的影响。

The effect of taste masking agents on in situ gelling pectin formulations for oral sustained delivery of paracetamol and ambroxol.

作者信息

Miyazaki Shozo, Kubo Wataru, Itoh Kunihiko, Konno Yasuhiro, Fujiwara Mariko, Dairaku Masatake, Togashi Mitsuo, Mikami Ryozo, Attwood David

机构信息

Faculty of Pharmaceutical Sciences, Health Science University of Hokkaido, Ishikari-Tohbetsu, Hokkaido 061-0293, Japan.

出版信息

Int J Pharm. 2005 Jun 13;297(1-2):38-49. doi: 10.1016/j.ijpharm.2005.02.029. Epub 2005 Apr 25.

Abstract

The aim of this study was to examine the influence of polyhydric alcohols (taste masking agents) on the rheological properties of in situ gelling pectin formulations and on the in vitro and in vivo release of paracetamol and ambroxol from these formulations. Gelation of orally administered pectin solutions containing calcium in complexed form occurred on release of calcium in the acidic environment of the stomach. Inclusion of 10% (w/v) sorbitol in 2% (w/v) pectin sols reduced the viscosity and ensured Newtonian flow properties. Xylitol and mannitol in similar concentrations were less effective in reducing viscosity; sucrose increased viscosity and caused non-Newtonian flow. The in vitro release of paracetamol from 2% (w/v) pectin gels formulated with 10% (w/v) of sorbitol, erythritol, xylitol or mannitol, and of ambroxol from 2% (w/v) pectin gels containing 10% (w/v) sorbitol, followed diffusion-controlled kinetics. Pectin gels (2%, w/v) containing sorbitol (10%, w/v) sustained the release of paracetamol in the rat stomach and bioavailabilities of approximately 90% of those from an orally administered paracetamol syrup were achieved. Sustained release of ambroxol from in situ gelling formulations was achieved with pectin concentrations of 1.5 and 1% (w/v) and a sorbitol concentration of 10% (w/v).

摘要

本研究的目的是考察多元醇(掩味剂)对原位凝胶化果胶制剂流变学性质的影响,以及对这些制剂中对乙酰氨基酚和氨溴索体外及体内释放的影响。口服的含有络合形式钙的果胶溶液在胃的酸性环境中钙释放时发生凝胶化。在2%(w/v)果胶溶胶中加入10%(w/v)山梨醇可降低粘度并确保牛顿流体性质。类似浓度的木糖醇和甘露醇在降低粘度方面效果较差;蔗糖增加粘度并导致非牛顿流体流动。由10%(w/v)山梨醇、赤藓糖醇、木糖醇或甘露醇配制的2%(w/v)果胶凝胶中对乙酰氨基酚的体外释放,以及含有10%(w/v)山梨醇的2%(w/v)果胶凝胶中氨溴索的体外释放,均遵循扩散控制动力学。含有10%(w/v)山梨醇的2%(w/v)果胶凝胶在大鼠胃中实现了对乙酰氨基酚的缓释,生物利用度达到口服对乙酰氨基酚糖浆生物利用度的约90%。通过1.5%和1%(w/v)的果胶浓度以及10%(w/v)的山梨醇浓度,实现了原位凝胶化制剂中氨溴索的缓释。

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