Nanotechnology Characterization Laboratory, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
Methods Mol Biol. 2024;2789:67-73. doi: 10.1007/978-1-0716-3786-9_7.
Ion concentration in liposomal drugs is important for drug stability and drug release profile. However, quantifying ion concentration in liposomal drugs is challenging due to the absence of chromophores or fluorophores of ions and the efficiency of their release from the liposome structure. To address these issues, a method based on reversed-phase high-performance liquid chromatography (RP-HPLC) coupled with a charged aerosol detector (CAD) has been developed to determine total, internal, and external ions in drug-loaded liposomal products. In this protocol, we focused on the quantitation of ammonium and sulfate ions in liposomal products, using generic PEGylated liposomal doxorubicin as an example. This method can be extended to calcium, acetate, and other ions in different liposomal formulations with slight modifications.
脂质体药物中的离子浓度对于药物稳定性和药物释放特性非常重要。然而,由于离子缺乏发色团或荧光团,以及其从脂质体结构中释放的效率,定量脂质体药物中的离子浓度具有挑战性。为了解决这些问题,已经开发了一种基于反相高效液相色谱(RP-HPLC)与带电气溶胶检测器(CAD)相结合的方法,用于测定载药脂质体产品中的总离子、内部离子和外部离子。在本方案中,我们专注于用通用的 PEG 化多柔比星脂质体作为示例,定量脂质体产品中的铵离子和硫酸根离子。此方法可以通过轻微修改扩展到不同脂质体配方中的钙、醋酸盐和其他离子。