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用于肠胃外给药的尼美舒利的助水溶作用。

Hydrotropic solubilization of nimesulide for parenteral administration.

作者信息

Agrawal Shikha, Pancholi S S, Jain N K, Agrawal G P

机构信息

Department of Pharmaceutical Sciences, Pharmaceutics Research laboratory, Dr. H.S. Gour University, Sagar 470 003, MP, India.

出版信息

Int J Pharm. 2004 Apr 15;274(1-2):149-55. doi: 10.1016/j.ijpharm.2004.01.012.

Abstract

Nimesulide is a non-steroidal anti-inflammatory drug (NSAID) that exhibits analgesic, antipyretic and anti-inflammatory activities. It is practically insoluble in water. The effect of various hydrotropes such as nicotinamide, sodium ascorbate, sodium benzoate, sodium salicylate and piperazine on the solubility of nimesulide was investigated. The solubility enhancement of nimesulide by the hydrotropes was observed in decreasing order as piperazine > sodium ascorbate > sodium salicylate > sodium benzoate > nicotinamide. In order to elucidate the probable mechanism of solubilization, various solution properties of hydrotropes such as viscosity, specific gravity, surface tension, refractive index, specific conductance of hydrotropic solutions were studied at 25 +/- 2 degrees C on the basis of earlier studies. The hydrotropic solubilization of nimesulide at lower hydrotrope concentration may be attributed to weak ionic interactions while that at higher hydrotrope concentration may be due to molecular aggregation. Parenteral formulations using piperazine as a hydrotrope were developed and studied for physical and chemical stability.

摘要

尼美舒利是一种具有镇痛、解热和抗炎活性的非甾体抗炎药(NSAID)。它几乎不溶于水。研究了烟酰胺、抗坏血酸钠、苯甲酸钠、水杨酸钠和哌嗪等各种助溶剂对尼美舒利溶解度的影响。观察到助溶剂对尼美舒利溶解度的增强作用按以下顺序递减:哌嗪>抗坏血酸钠>水杨酸钠>苯甲酸钠>烟酰胺。为了阐明可能的增溶机制,根据早期研究,在25±2℃下研究了助溶剂的各种溶液性质,如水溶液的粘度、比重、表面张力、折射率、电导率。较低助溶剂浓度下尼美舒利的助溶作用可能归因于弱离子相互作用,而较高助溶剂浓度下的助溶作用可能是由于分子聚集。开发了以哌嗪作为助溶剂的注射剂,并对其物理和化学稳定性进行了研究。

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