Applications of Lipid-based Nanocarriers for Parenteral Drug Delivery

被引:8
|
作者
Santonocito, Debora [1 ]
Puglia, Carmelo [1 ]
机构
[1] Univ Catania, Dept Drug & Hlth Sci, Viale Andrea Doria 6, I-95125 Catania, Italy
关键词
Lipid nanoparticles; phytocompounds; synthetic drugs; parenteral drug delivery; mRNA vaccine; Covid-19; MODIFIED MESSENGER-RNA; IN-VITRO; NANOPARTICLES SLN; GELATIN NANOPARTICLES; BINARY-MIXTURES; CARRIER SYSTEM; BREAST-CANCER; PARTICLE-SIZE; FORMULATION; PHARMACOKINETICS;
D O I
10.2174/0929867329666220104111949
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review describes the use of lipid-based nanocarriers (LNCs) for the parenteral delivery of pharmaceutical actives. Firstly, the two generations of LNCs, namely solid lipid nanoparticles (SLNs) and nanostructured lipid carriers (NLCs), are explained in terms of preparation, characterization and stability. Although the use of LNCs through parenteral administration has shown many benefits, their use is limited by opsonization, an immune process that causes their short half-life (3-5 min). Therefore, many strategies are discussed to realize "stealth" systems suitable for parenteral administration. The requirements and applications of parenteral lipid nanoparticles are reviewed for the delivery of natural compounds, synthetic drugs and genetic materials. Recently, the latter application has been of remarkable interest due to the numerous benefits of mRNA vaccines to fight the Covid-19 pandemic.
引用
收藏
页码:4152 / 4169
页数:18
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