Study of release kinetics and degradation thermodynamics of ferric citrate liposomes

化学 动力学 脂质体 吸热过程 小泡 生物利用度 色谱法 Zeta电位 粒径 化学工程 纳米颗粒 有机化学 生物化学 物理化学 药理学 医学 物理 吸附 量子力学 工程类
作者
Shan Wang,Wenxin Li,Kaiyue Sun,Ru Zhang,Shuping Wang,Li‐Na Geng
出处
期刊:Chemistry and Physics of Lipids [Elsevier]
卷期号:225: 104811-104811 被引量:16
标识
DOI:10.1016/j.chemphyslip.2019.104811
摘要

Ferric citrate liposome (FAC-Lip) with good sustained-released property was prepared by the rotary-evaporated film-ultrasonic method, and characterized by TEM, DLS, zeta potential and encapsulation efficiency (EE%). The effects of membrane material ratios (mPC: mchol = 8:1, 10:1 and 12:1) and drug lipid ratios (mFAC: mPC = 1:4, 1:6.5 and 1:8) on the release of FAC-Lip were examined. The in vitro release kinetic models and mechanisms of FAC-Lip in artificial gastric juice (SGF) and artificial intestinal juice (SIF) compared with free-FAC were determined. The thermal degradation in PBS was also determined. The results showed that FAC-Lip with membrane material ratio (10:1) and drug lipid ratio (1:6.5) had the optimal sustained-released property, unilamellar vesicles with uniform size (178 ± 2.12 nm), negative charge (−56 ± 3.51 mV) and high encapsulation efficiency (72.77 ± 0.42%). The in vitro release kinetic models of FAC-Lip were two-phase kinetics model and the release mechanisms were non-Fick diffusion both in SGF and SIF. The thermal degradation of FAC-Lip was an endothermic and spontaneous reaction. The results may be helpful in optimizing drug-liposome design, application in food and medicine industries, and furthermore, predicting and guiding medication in vivo.
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