Laboratory for Pharmacotechnology and Biopharmacy, Katholieke Universiteit Leuven, BE-3000 Leuven, Belgium.
J Pharm Sci. 2012 Jan;101(1):7-9. doi: 10.1002/jps.22750. Epub 2011 Sep 23.
An emerging technology subtype that has been adopted by formulators to address low-solubility issues is the supersaturating drug delivery system; this system is based on the "spring" and "parachute" design elements, which have been applied to lipid-based formulations, S(M)EDDS, solid dispersions, nano-based systems, and many others. This broad formulation approach attempts to delicately balance the need of creating intraluminal drug concentrations in excess of its thermodynamic solubility while at the same time providing for sufficient solution stability to allow for useful drug absorption. The conundrum created is that the higher the extent of supersaturation, the lower the physical stability of the metastable solution based on an increased tendency for a solubilized drug to precipitate. Traditional dissolution testing is a touchstone of formulation development based on the need for useful dissolution rates and drug availability. Dissolution testing is likewise important in the development and characterization of enabling and supersaturating drug delivery systems; however, their execution and interpretation are distinct from that associated with conventional dosage forms. The nature of the dissolution assay (sink versus nonsink, apparatus type, and rate and extent of supersaturation) can impact the ability to efficiently use the dissolution data in the configuration of these enabling formulations.
一种新兴的技术类型,已被制剂商采用来解决低溶解度问题,即超饱和药物传递系统;该系统基于“弹簧”和“降落伞”设计元素,已应用于基于脂质的制剂、S(M)EDDS、固体分散体、纳米系统等。这种广泛的制剂方法试图巧妙地平衡在创造腔内药物浓度超过其热力学溶解度的同时,为提供足够的溶液稳定性以允许有用的药物吸收之间的需求。所产生的难题是,超饱和度越高,基于溶解药物沉淀倾向增加的亚稳溶液的物理稳定性越低。传统的溶解试验是制剂开发的基石,基于对有用的溶解速率和药物可用性的需求。溶解试验同样在开发和表征使能和超饱和药物传递系统中很重要;然而,它们的执行和解释与传统剂型相关的执行和解释不同。溶解试验的性质(溶出池与非溶出池、仪器类型、以及超饱和度的速率和程度)可能会影响在这些使能制剂构型中有效利用溶解数据的能力。