School of Pharmacy and Pharmaceutical Sciences, University of California at San Diego, La Jolla, 92093, USA.
J Control Release. 2013 Nov 10;171(3):308-14. doi: 10.1016/j.jconrel.2013.06.018. Epub 2013 Jun 20.
Though accurately evaluating the kinetics of release is critical for validating newly designed therapeutic carriers for in vivo applications, few methods yet exist for release measurement in real time and without the need for any sample preparation. Many of the current approaches (e.g. chromatographic methods, absorption spectroscopy, or NMR spectroscopy) rely on isolation of the released material from the loaded vehicles, which require additional sample purification and can lead to loss of accuracy when probing fast kinetics of release. In this study we describe the use of time-resolved fluorescence for in situ monitoring of small molecule release kinetics from biodegradable polymeric drug delivery systems. This method relies on the observation that fluorescent reporters being released from polymeric drug delivery systems possess distinct excited-state lifetime components, reflecting their different environments in the particle suspensions, i.e., confined in the polymer matrices or free in the aqueous environment. These distinct lifetimes enable real-time quantitative mapping of the relative concentrations of dye in each population to obtain precise and accurate temporal information on the release profile of particular carrier/payload combinations. We found that fluorescence lifetime better distinguishes subtle differences in release profiles (e.g. differences associated with dye loading) than conventional steady-state fluorescence measurements, which represent the averaged dye behavior over the entire scan. Given the method's applicability to both hydrophobic and hydrophilic cargo, it could be employed to model the release of any drug-carrier combination.
尽管准确评估释放动力学对于验证新设计的治疗载体在体内应用至关重要,但目前还很少有方法能够实时进行释放测量,而无需进行任何样品制备。许多当前的方法(例如色谱方法、吸收光谱或 NMR 光谱)依赖于从负载载体中分离释放的材料,这需要额外的样品纯化,并且在探测快速释放动力学时可能导致准确性降低。在这项研究中,我们描述了使用时间分辨荧光原位监测可生物降解聚合物药物传递系统中小分子释放动力学。该方法依赖于这样一个观察结果,即从聚合物药物传递系统中释放的荧光报告剂具有不同的激发态寿命成分,反映了它们在颗粒悬浮液中的不同环境,即在聚合物基质中受限或在水性环境中自由。这些不同的寿命使我们能够实时定量映射每种染料在各群体中的相对浓度,从而获得有关特定载体/有效载荷组合释放曲线的精确和准确的时间信息。我们发现,荧光寿命比传统的稳态荧光测量更好地区分释放曲线的细微差异(例如与染料负载相关的差异),因为传统的稳态荧光测量代表了整个扫描过程中染料的平均行为。鉴于该方法适用于疏水性和亲水性货物,它可以用于模拟任何药物载体组合的释放。