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负载荧光标记环孢素A的固体脂质纳米粒:体外抗炎活性

Solid lipid nanoparticles loaded with fluorescent-labelled Cyclosporine A: anti-inflammatory activity in vitro.

作者信息

Gallarate Marina, Serpe Loredana, Foglietta Federica, Zara Gian Paolo, Giordano Susanna, Peira Elena, Chirio Daniela, Battaglia Luigi

机构信息

Universita degli Studi di Torino, Dipartimento di Scienza e Tecnologia del Farmaco, Via Pietro Giuria 9, Torino, Italy.

出版信息

Protein Pept Lett. 2014;21(11):1157-62. doi: 10.2174/0929866521666140806164410.

Abstract

FMOC-isocyclosporine A, a fluorescent labeled cyclosporine A, was encapsulated in solid lipid nanoparticles (SLN) prepared by the coacervation technique, and its anti-inflammatory activity was evaluated. The anti-inflammatory activity of the fluorescent labelled molecule, measured as inhibition of TNF-α secretion, is similar to the native one. SLN were compared to commercial formulations, through measurement of cytokine release and drug uptake in rat peripheral blood mononuclear cells. Drug-loaded SLN inhibit TNF-α secretion in a lower extent than commercial formulations, probably due to a lower uptake by the cells, but the increase of IL-10 secretion caused by the lipid matrix itself makes this formulation interesting for its anti-inflammatory activity.

摘要

芴甲氧羰基-异环孢素A(一种荧光标记的环孢素A)被包裹于通过凝聚技术制备的固体脂质纳米粒(SLN)中,并对其抗炎活性进行了评估。以抑制肿瘤坏死因子-α(TNF-α)分泌来衡量,荧光标记分子的抗炎活性与天然分子相似。通过测量大鼠外周血单核细胞中的细胞因子释放和药物摄取,将SLN与市售制剂进行了比较。载药SLN抑制TNF-α分泌的程度低于市售制剂,这可能是由于细胞摄取较少,但脂质基质本身引起的白细胞介素-10(IL-10)分泌增加使得该制剂因其抗炎活性而具有吸引力。

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