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首页> 外文期刊>International Journal of Pharmaceutics >Cyclodextrins: Efficient biocompatible solubilizing excipients for bromhexine liquid and semi-solid drug delivery systems
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Cyclodextrins: Efficient biocompatible solubilizing excipients for bromhexine liquid and semi-solid drug delivery systems

机译:环糊精:用于溴己辛液体和半固体药物递送系统的高效生物相容性增溶赋形剂

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摘要

Bromhexine hydrochloride (bromhexine) is a mucolytic agent with very low aqueous solubility. However, with addition of cyclodextrins (CD) to the formulation, this disadvantage may be limited and therapeutic doses of bromhexine in solution can be achieved. The interaction of bromhexine with α-, β-, γ- and sulfobutylether (SBE)-β-CD, respectively, was elucidated by means of phase solubility diagrams and calorimetric analysis. The complexes were further characterized by size, and the effect of the CD concentrations used was evaluated in a viability assay. From phase solubility diagrams with α-, β-, γ- and SBE-β-CD and bromhexine, it was determined that the solubility of bromhexine significantly increased with addition of CDs, showing an A L type solubility curve for bromhexine/α- and β-CD, and an A N type for bromhexine/γ- and SBE-β-CD. The highest soluble concentrations of bromhexine were achieved with α- and SBE-β-CD, i.e. when using a 100 mM α- or SBE-β-CD solution, 4 and 5.5 times more bromhexine was solubilized, respectively, compared to pure aqueous solubilization of bromhexine. The apparent association constants determined from the phase solubility studies showed very low values of 34, 17, 8 and 156 M -1 for bromhexine/α-, β-, γ- and SBE-β-CD, respectively, as compared to the association constants determined by ITC which exhibited values of 89, 307 and 1680 M -1 for bromhexine/α-, β- and SBE-β-CD, respectively. The formation of aggregates aided solubilization of bromhexine in the phase solubility studies explaining the difference in the association constants between the two methods. Due to very low signal to noise ratio, no information was extracted for bromhexine/γ-CD solutions from the ITC measurements. The effect on cellular viability of the CDs ranked β- α- SBE-β- γ-CD. In conclusion, the results altogether demonstrated that SBE-β-CD is the most suitable CD for future drug delivery systems from the aspect of high amounts of solubilized bromhexine and high safety of the SBE-β-CD.
机译:盐酸溴己新(bromhexine)是一种水溶性很低的粘液溶解剂。但是,在制剂中添加环糊精(CD)可以限制这一缺点,并且可以达到溶液中溴己定的治疗剂量。通过相溶解度图和量热分析,阐明了溴己辛分别与α-,β-,γ-和磺丁基醚(SBE)-β-CD的相互作用。通过大小进一步表征复合物,并在生存力测定中评估所用CD浓度的影响。从具有α-,β-,γ-和SBE-β-CD和溴己辛的相溶度图可以确定,溴化己辛的溶解度随CD的添加而显着增加,显示了溴己辛/α-和β的AL型溶解度曲线-CD,以及溴己己/γ-和SBE-β-CD的AN型。用α-和SBE-β-CD可以达到最高的溴己定可溶浓度,即,当使用100 mMα-或SBE-β-CD溶液时,与纯水溶增溶相比,溴己定的溶解度分别提高了4倍和5.5倍溴己定。根据相溶解度研究确定的表观缔合常数显示,与缔合相比,溴己辛/α-,β-,γ-和SBE-β-CD的值分别非常低,分别为34、17、8和156 M -1由ITC确定的常数,其对溴己辛/α-,β-和SBE-β-CD分别显示89、307和1680 M -1的值。在相溶解度研究中,聚集体的形成有助于溴己辛的增溶,这解释了两种方法之间缔合常数的差异。由于信噪比非常低,因此无法从ITC测量中提取出有关溴己辛/γ-CD溶液的信息。 CD对细胞生存力的影响排列为β->α->SBE-β->γ-CD。总之,从高溶解性溴己定的量和SBE-β-CD的高安全性方面来看,结果完全表明SBE-β-CD是最适合未来药物递送系统的CD。

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