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首页> 外文期刊>Acta pharmaceutica: a quarterly journal of Croatian Pharmaceutical Society and Slovenian Pharmaceutical Society, dealing with all branches of pharmacy and allied sciences >Clozapine-carboxylic acid plasticized co-amorphous dispersions: Preparation, characterization and solution stability evaluation
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Clozapine-carboxylic acid plasticized co-amorphous dispersions: Preparation, characterization and solution stability evaluation

机译:氯氮平-羧酸增塑共非晶分散体:制备,表征和溶液稳定性评估

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摘要

This study addressed the possibility of forming of co-amorphous systems between clozapine (CZ) and various carboxylic acid plasticizers (CAPs). The aim was to improve the solubility and oral bioavailability of clozapine. Co-amorphous dispersions were prepared using modified solvent evaporation methodology at drug/plasticizer stoichiometric ratios of 1: 1, 1: 1.5 and 1:2. Solid state characterization was performed using differential scanning calorimetry, X-ray diffraction and infra red spectroscopy. Highly soluble homogeneous co-amorphous dispersions were formed between clozapine and CAPs via hydrogen bonding. The co-amorphous dispersions formed with tartaric acid (1: 2) showed the highest dissolution percentage (> 95 % in 20 minutes) compared to pure crystalline CZ (56 %). Highly stable solutions were obtained from co-amorphous CZ-citric and CZ-tartaric acid at 1: 1.5 molar ratio. The prepared dispersions suggest the possibility of peroral or sublingual administration of highly soluble clozapine at a reduced dose with the great chance to bypass the first pass metabolism.
机译:这项研究解决了在氯氮平(CZ)与各种羧酸增塑剂(CAP)之间形成共非晶体系的可能性。目的是提高氯氮平的溶解度和口服生物利用度。使用改进的溶剂蒸发方法以药物/增塑剂化学计量比为1:1、1:1.5和1:2制备共非晶分散液。使用差示扫描量热法,X射线衍射和红外光谱法进行固态表征。通过氢键在氯氮平和CAP之间形成了高度溶解的均质共非晶分散体。与纯结晶CZ(56%)相比,与酒石酸(1:2)形成的共非晶分散液显示出最高的溶解百分比(在20分钟内> 95%)。从共非晶的CZ-柠檬酸和CZ-酒石酸以1:1.5的摩尔比获得高度稳定的溶液。制备的分散液表明,口服或舌下高溶解度的氯氮平可以降低剂量,但有很大的机会绕过首过代谢。

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