Università degli Studi di Perugia, Dipartimento di Chimica e Tecnologia del Farmaco, Via del Liceo 1, 06123 Perugia, Italy.
J Pharm Biomed Anal. 2014 Jan;87:62-81. doi: 10.1016/j.jpba.2013.06.029. Epub 2013 Jul 4.
With the discovery of the bile acid (BA)-activated nuclear and membrane receptors, the role of BAs as signalling molecules in important paracrine and endocrine networks has been fully documented in the last decade. Besides regulating their own synthesis and transport, BAs have been demonstrated being involved in triggering the adaptive response to cholestasis and other insults to liver. More to the point, their recognized ability to control the general energy-related metabolism and inflammation processes has contributed to justify the renewed interest towards this class of amphiphilic steroidal compounds. All these evidences feed a continuing interest in the BA research aimed at designing and synthesizing new side chain- and body-modified derivatives endowed with improved biological and physico-chemical profiles, as well as with proper ADMET behaviour. In this context, the micellar aggregation of BAs, and the respective critical micellization concentration (CMC) value (determined on the BA sodium salt, BS), is considered a key parameter that needs to be determined in the preliminary phase of compound characterization, being implicated in cytotoxicity issues. An extraordinary variety of different analytical techniques and methods have been proposed along the years with the aim of better identifying the start of the self-aggregation process of BS monomers. The unicity of the physico-chemical nature of such class of compounds can be invoked to explain this unusual interest. Accordingly, a number of both invasive and non-invasive approaches have been developed along with a limited number of indirect chromatographic-based estimation strategies. Worth to be mentioned among the non-invasive determination methods are those based on potentiometry, freezing point depression, surface tension, nuclear magnetic resonance, viscosimetry, turbidimetry, microcalorimetry, refractometry, conductimetry, spectrophotometry, cholesterol solubilization, and monoglucuronide solubilization. Dye solubilization- and fluorescence-based methods deserve instead credit among the invasive methodological approaches. Indirect chromatographic methods based on capillary electrophoresis and high performance liquid chromatography analysis also demonstrated to be profitably exploited for the CMC estimation, especially when a small amount of sample is available. The collection of literature data reveals that the CMC value of a given BS is markedly related to the method selected for determining it as well as to the experimental conditions applied during the analysis.
随着胆酸 (BA)-激活的核受体和膜受体的发现,BA 作为旁分泌和内分泌网络中的信号分子的作用在过去十年中得到了充分的证明。除了调节自身的合成和运输外,BA 已被证明参与触发对胆汁淤积和其他肝脏损伤的适应性反应。更重要的是,它们控制一般能量相关代谢和炎症过程的能力已被证明是 justifies 对这一类两亲性甾体化合物重新产生兴趣的原因。所有这些证据都促使人们对 BA 研究产生持续的兴趣,旨在设计和合成具有改善的生物学和物理化学特性以及适当的 ADMET 行为的新的侧链和主体修饰衍生物。在这种情况下,BA 的胶束聚集及其相应的临界胶束浓度 (CMC) 值(在 BA 钠盐 BS 上确定)被认为是在化合物表征的初步阶段需要确定的关键参数,因为它涉及细胞毒性问题。多年来,已经提出了许多不同的分析技术和方法,旨在更好地确定 BS 单体自聚集过程的开始。可以援引此类化合物独特的物理化学性质来解释这种不寻常的兴趣。因此,已经开发了许多侵入性和非侵入性方法,以及有限数量的间接基于色谱的估计策略。在非侵入性测定方法中值得一提的是那些基于电位法、冰点降低法、表面张力法、核磁共振法、粘度法、比浊法、微量热法、折射法、电导率法、分光光度法、胆固醇溶解法和单葡萄糖醛酸溶解法。染料溶解法和荧光法作为侵入性方法在其中也占有一席之地。基于毛细管电泳和高效液相色谱分析的间接色谱方法也被证明可用于 CMC 估计,特别是当有少量样品可用时。文献数据的收集表明,给定 BS 的 CMC 值与用于确定它的方法以及在分析过程中应用的实验条件显著相关。