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首页> 外文期刊>Journal of Inclusion Phenomena and Macrocyclic Chemistry >Study of inclusion complex formation between a cationic surfactant, two cyclodextrins and a drug
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Study of inclusion complex formation between a cationic surfactant, two cyclodextrins and a drug

机译:阳离子表面活性剂,两种环糊精与药物之间包合物形成的研究

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In this study inclusion of hexadecyltrimethylam-monium bromide (HTAB) with α-, and β-cyclodextrin (CD) in the presence and the absence of bromhexine (BH) was investigated using ion-selective electrode method. The association constants of HTAB with CDs were determined by potentiometry and were close to literature values. The obtained results indicated that α-CD formed 1:1 and 1:2 inclusion complexes, but β-CD formed only a 1:1 inclusion complex. In the presence of drug, the interaction between CDs and HTAB decreased, because both drug and HTAB could interact with CDs. The results showed that the interaction between drug and CDs are greater than HTAB and CDs. The stoichiometry of the inclusion complexes, the critical aggregation concentration (CAC), the monomer surfactant concentration of HTAB, [HTAB]_f, and also the effect of the inclusion complex on the micellization process of the HTAB were determined by conductivity measurements.
机译:在这项研究中,使用离子选择电极法研究了十六烷基三甲基溴化铵(HTAB)与α-和β-环糊精(CD)在存在和不存在的情况下的结合情况。 HTAB与CD的缔合常数通过电位法测定,接近文献值。获得的结果表明,α-CD形成1:1和1:2的包合物,而β-CD仅形成1:1的包合物。在存在药物的情况下,CD和HTAB之间的相互作用降低,因为药物和HTAB都可以与CD相互作用。结果表明,药物与CD的相互作用大于HTAB和CD。通过电导率测量来确定包合物的化学计量,临界聚集浓度(CAC),HTAB的单体表面活性剂浓度,[HTAB] _f以及包合物对HTAB胶束化过程的影响。

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