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首页> 外文期刊>Biophysical Chemistry: An International Journal Devoted to the Physical Chemistry of Biological Phenomena >Studies on the size and stability of chlorpromazine hydrochloride nanostructures in aqueous solution.
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Studies on the size and stability of chlorpromazine hydrochloride nanostructures in aqueous solution.

机译:研究盐酸氯丙嗪纳米结构在水溶液中的大小和稳定性。

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摘要

The mean aggregate number (MAN) of the antipsychotic drug chlorpromazine hydrochloride (CPZ) nanostructure was investigated by fluorescence quenching using 9-methylanthracene (9-MA) as the quencher. The method was designed to take advantage of the intrinsic fluorescent properties of CPZ. The validity of this method was supported by the results obtained for the MAN which was determined to be approximately 37 for a solution of 10 mM CPZ in 0.1 M pH 6.5 phosphate buffer. An increase in the aggregate size with increasing drug concentration confirmed the stepwise aggregation theory of CPZ micelle formation. Differential scanning calorimetry was used to examine the effects of concentration on the thermodynamics of micellization. The enthalpy of demicellization increased with increasing CPZ concentration (5-12 mM), suggesting a greater stability of the aggregates at higher concentrations. At amphiphile concentrations higher than 12 mM, a plateau of approximately 10 kJ/mol was observed as the enthalpy of demicellization. Fluorescence lifetime results revealed a two-component system at low CPZ concentration, while data at amphiphile concentrations higher than 12 mM could not be fitted to either single or multi-component lifetime values, suggesting an increase in dispersity in these nanostructures at higher CPZ concentrations. Temperatures higher than 40 degrees C tend to destabilize the larger micelles, and demicellization was observed after approximately 45 degrees C. Changes in osmotic pressure in the presence of dextrose up to 0.3 M had no significant effect on the size of these micellar nanostructures.
机译:抗精神病药盐酸氯丙嗪(CPZ)纳米结构的平均聚集数(MAN)通过使用9-甲基蒽(9-MA)作为猝灭剂的荧光猝灭进行研究。设计该方法以利用CPZ的固有荧光特性。该方法的有效性得到了MAN的结果的支持,该结果对于10 mM CPZ在0.1 M pH 6.5磷酸盐缓冲液中的溶液确定为大约37。随着药物浓度的增加,聚集体尺寸的增加证实了CPZ胶束形成的逐步聚集理论。差示扫描量热法用于检查浓度对胶束热力学的影响。随着CPZ浓度(5-12 mM)的增加,去离子化的焓增加,表明在较高浓度下聚集体的稳定性更高。在两亲物浓度高于12 mM时,观察到大约10 kJ / mol的平稳期是去离子化的焓。荧光寿命结果表明,低CPZ浓度下为双组分系统,而两亲物浓度高于12 mM的数据无法拟合为单组分或多组分寿命值,表明在较高CPZ浓度下这些纳米结构的分散性增加。高于40摄氏度的温度往往会破坏较大的胶束的稳定性,并且在约45摄氏度后会观察到脱细胞作用。在葡萄糖浓度高达0.3 M的情况下,渗透压的变化对这些胶束纳米结构的尺寸没有明显影响。

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