Development of a concentration-controlled sequential nanoprecipitation for making lipid nanoparticles with high drug loading  被引量:1

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作  者:Letao Xu Xing Wang Guangze Yang Zihan Zhao Yilun Weng Yang Li Yun Liu Chun-Xia Zhao 

机构地区:[1]Australian Institute for Bioengineering and Nanotechnology,The University of Queensland,St.Lucia,Queensland,Australia [2]School of Chemical Engineering,Faculty of Sciences,Engincering and Technology,The University of Adelaide,Adelaide,South Australia,Australia

出  处:《Aggregate》2023年第6期71-84,共14页聚集体(英文)

基  金:Australian Research Council Projects,Grant/Award Number:DP200101238;Australian National Health and Medical Research Council projects of Australia,Grant/Award Number:APP2008698;Australian Research Council Discovery Early Career Researcher Award,Grant/Award Number:DE230101044;Australian Government Research Training Program Scholarships。

摘  要:Lipid-based nanostructures have garnered considerable interests over the last two decades,and have achieved tremendous clinical success including thefirst clinical approval of a liposome(Doxil)for cancer therapy in 1995 and the recent COVID-19 mRNA lipid nanoparticle vaccines.Compared to liposomes which have a lipid bilayer surrounding an aqueous core,lipid nanoparticles with a particle structure have several attractive advantages for encapsulating poorly water-soluble drugs such as better stability due to the particle structure,high drug encapsulation efficiency because of a pre-or co-drug-loading strategy.While many studies have reported the synthesis of lipid nanoparticles for hydrophobic drug encapsulation,the pre-cise control of drug loading and encapsulation efficiency remains a significant challenge.This work reports a new concentration-controlled nanoprecipitation plat-form technology for fabricating lipid nanoparticles with tunable drug loading up to 70 wt%.This method is applicable for encapsulating a wide range of drugs from very hydrophobic to slightly hydrophilic.Using this facile method,nanoparticles with tunable drug loading exhibited excellent properties such as small particle size,narrow size distribution,good particle stability,showing great promise for future drug delivery applications.

关 键 词:controlled release drug delivery drug loading lipid nanoparticles NANOPRECIPITATION 

分 类 号:O62[理学—有机化学]

 

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