体内分布
生物利用度
Zeta电位
药代动力学
体内
化学
纳米囊
分散性
纳米载体
药物输送
肺表面活性物质
药理学
分布(数学)
粒径
色谱法
纳米技术
纳米颗粒
体外
材料科学
有机化学
生物化学
数学
医学
物理化学
数学分析
生物技术
生物
作者
Veronia R. Ayoub,Mona M.A. Abdel-Mottaleb,Ismail T. Ibrahem,M. A. Motaleb,Ahmed S. Geneidi
标识
DOI:10.1002/ardp.202300618
摘要
Abstract Lipid nanocapsules (LNCs) are lipid nanocarriers developed for drug delivery enhancement. The antidepressant drug desvenlafaxine (DSV) was entrapped in LNC to improve its brain delivery. Different DSV‐loaded LNCs formulae using different oils and surfactants were studied to obtain the optimum formula for further studies. In vivo biodistribution studies were done using Swiss albino mice by intravenous injection of DSV‐loaded LNCs by radioiodination technique. The optimum DSV‐loaded LNC formula was obtained by using Labrafil® M1944CS as the oil and Solutol® HS15 as the surfactant in the ratio of 1:1, with a particle size of 34.28 ± 0.41 nm, a polydispersity index of 0.032 ± 0.05, a zeta potential of −25.77 ± 1.41, and good stability for up to 6 months. The in vivo biodistribution and pharmacokinetics data ensure the bioavailability improvement for DSV brain delivery as C max and AUC (1– t ) increased more than double for intravenously DSV‐loaded LNCs compared with the DSV solution. In conclusion, the results obtained from this study give an insight into the great potential of using DSV‐loaded LNC for the enhancement of brain delivery.
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