PLGA公司
乙醇酸
纳米颗粒
内吞作用
乳状液
化学工程
材料科学
溶解
蒸发
粒径
乳酸
溶剂
免疫系统
化学
生物物理学
纳米技术
有机化学
生物化学
细胞
免疫学
工程类
细菌
物理
热力学
生物
遗传学
作者
Lennart Pusch,Regine Brox,Karl Scheuer,Tadahiro Yokosawa,Mingjian Wu,Benjamin Apeleo Zubiri,Erdmann Spiecker,Klaus D. Jandt,Dagmar Fischer,Holger Hackstein
出处
期刊:Nanomedicine
[Future Medicine]
日期:2021-09-15
卷期号:16 (23): 2075-2094
被引量:4
标识
DOI:10.2217/nnm-2021-0022
摘要
Background: Poly(lactic-co-glycolic) acid (PLGA) nanoparticles can be prepared by emulsion-solvent-evaporation from o/w and w1/o/w2 emulsions. Aims: To elaborate similarities and differences regarding mechanical, morphological and physicochemical properties, as well as endocytosis and dose-dependent immune responses by primary human leukocytes between nanoparticles prepared by these two methods. Methods: Fluorescently labeled as well as TLR agonist (R848)-loaded PLGA nanoparticles were prepared via both single- and double-emulsion solvent evaporation. Results: Particles prepared by both methods were similar in chemical composition and surface charge but exhibited slight differences in size and morphology. Pronounced differences were found for loading, dissolution and mechanical properties. The particles were differently endocytosed by monocytes and induced qualitatively and quantitatively different immune responses. Conclusions: Variations in nanoparticle preparation can affect particle-derived immunological characteristics.
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