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Size-dependent cellular uptake and sustained drug release of PLGA particles
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作者 Rui Sun Xia Liu +3 位作者 Yu Zhang Qian Li Ying Zhu Chunhai Fan 《Particuology》 SCIE EI CAS CSCD 2023年第2期1-7,共7页
Poly(lactic-co-glycolic)acid(PLGA)particles have become a commonly used drug delivery strategy in the pharmaceutical industry.In this work,we aim to investigate the size-dependent cellular internalization of PLGA part... Poly(lactic-co-glycolic)acid(PLGA)particles have become a commonly used drug delivery strategy in the pharmaceutical industry.In this work,we aim to investigate the size-dependent cellular internalization of PLGA particles and its effects on sustained drug release.We prepared three different-sized particles using PLGA(200,500 and 2000 nm)ranging from submicrometer to micrometer.Dexamethasone(DEX)with excellent anti-inflammatory properties was used as a model drug to prepare DEX-loaded PLGA particles(DPs).We comprehensively investigated the encapsulation efficiency,cellular uptake and in vitro drug release profile.Pharmacodynamic assessment revealed that,in the lipopolysaccharide(LPS)-induced RAW 264.7 cells model,500 nm DPs showed sustained anti-inflammatory efficacy.This work provides important information for designing PLGA-based drug delivery systems for biomedical applications. 展开更多
关键词 dex-loaded PLGA particles(DPs) Sustained release Anti-inflammatory efficacy
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