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Celastrol-loaded macrophage membrane camouflaged PEG-PLGA nano-particles for targeted therapy of severe acute pancreatitis in rats
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Wei-zhen QIAO, Xi CAO, Zhi-rong ZHANG, Tao GONG, Yao FU*
Acta Pharmaceutica Sinica | 2018, 53(1) : 127 - 132
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Acta Pharmaceutica Sinica | 2018, 53(1): 127-132
ORIGINAL ARTICLES
Celastrol-loaded macrophage membrane camouflaged PEG-PLGA nano-particles for targeted therapy of severe acute pancreatitis in rats
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Wei-zhen QIAO, Xi CAO, Zhi-rong ZHANG, Tao GONG, Yao FU*
Affiliations
  • Key Laboratory of Drug Targeting and Drug Delivery Systems, West China School of Pharmacy, Sichuan University, Chengdu 610041, China
Published: 2018-01-12 doi: 10.16438/j.0513-4870.2017-0846
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Severe acute pancreatitis (SAP) is characterized by both local and systemic inflammatory responses. This study was designed to develop a site-specific delivery strategy for SAP therapy using celastrol (CLT). First, murine RAW264.7 cells were used as a model of macrophage cell line, cell membranes were obtained by emptying intracellular contents via hypotonic lysing, mechanical membrane disruption, and differential centrifugation. Poly(ethylene glycol) methyl ether-block-poly(lactic-co-glycolic acid) (PEG-PLGA) nanoparticles (NPs) were then prepared by sonication. With the collected membrane materials, macrophage membrane coated PEG-PLGA NPs (RNPs) were then prepared by extrusion through a 400 nm polycarbonate membrane. Biodistribution study in rats with SAP showed RNPs selectively accumulated in the inflamed pancreatic tissues. Compared with CLT loaded NPs, CLT loaded RNPs were proven to effectively attenuate local pancreatic inflammation and systemic inflammation in rats with SAP.

RAW264.7 macrophage  /  poly(ethylene glycol) methyl ether-block-poly(lactic-co-glycolic acid)  /  nanoparticle  /  celastrol  /  severe acute pancreatitis
Wei-zhen QIAO, Xi CAO, Zhi-rong ZHANG, Tao GONG, Yao FU. Celastrol-loaded macrophage membrane camouflaged PEG-PLGA nano-particles for targeted therapy of severe acute pancreatitis in rats[J]. Acta Pharmaceutica Sinica, 2018 , 53 (1) : 127 -132 . DOI: 10.16438/j.0513-4870.2017-0846
Year 2018 volume 53 Issue 1
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doi: 10.16438/j.0513-4870.2017-0846
  • Receive Date:2017-08-29
  • Online Date:2026-01-15
  • Published:2018-01-12
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  • Received:2017-08-29
  • Revised:2017-09-24
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    Key Laboratory of Drug Targeting and Drug Delivery Systems, West China School of Pharmacy, Sichuan University, Chengdu 610041, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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