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PEGylated phospholipid-coated polylactic acid-glycolic acid microspheres to escape the phagocytosis of alveolar macrophages
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Jia-qi LI1, Lu QIN1, Huang-liang ZHENG1, Xiao-ran LI2, MICHAEL Moehwald3, Lin CHEN4, Yu-yang ZHANG2, Shi-rui MAO1, *
Acta Pharmaceutica Sinica | 2019, 54(7) : 1303 - 1311
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Acta Pharmaceutica Sinica | 2019, 54(7): 1303-1311
Original Articles
PEGylated phospholipid-coated polylactic acid-glycolic acid microspheres to escape the phagocytosis of alveolar macrophages
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Jia-qi LI1, Lu QIN1, Huang-liang ZHENG1, Xiao-ran LI2, MICHAEL Moehwald3, Lin CHEN4, Yu-yang ZHANG2, Shi-rui MAO1, *
Affiliations
  • 1. School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China
  • 2. School of Life Sciences and Biological Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China
  • 3. Chemical and Pharmaceutical Development, Bayer AG D-42117, Germany
  • 4. Chemical and Pharmaceutical Development, Bayer AG, Beijing 100020, China
Published: 2019-07-12 doi: 10.16438/j.0513-4870.2019-0342
Outline
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Microspheres based on polylactic acid-glycolic acid (PLGA) copolymer have unique advantages in pulmonary controlled drug delivery. However, the clearance mechanism dominated by lung macrophage phagocytosis greatly limits the long-term retention of drugs in the deep lung. In order to avoid the scavenging effect of lung macrophages, the PLGA microspheres coated by polyethylene glycol-distearoyl-glycero-phosphoethanolamine (PEG-DSPE) was designed in this study, and the effect of chain length of PEG-DSPE and its ratio on the macrophage uptake was investigated. With coumarin 6 as a fluorescent probe, the coumarin 6-loaded PLGA microspheres was prepared by premix membrane emulsification/solvent evaporation. The particle size was controlled to 3-5 μm and the encapsulation efficiency was over 90%. After incubation in the cell culture fluid for 48 h, the in vitro leakage of fluorescein from the microspheres was less than 1.5%, eliminating the interference of free fluorescein on the cellular uptake. Murine macrophages RAW264.7 cell line was selected for the in vitro cell study. The preparations showed little toxicity to cells in the cytotoxicity study. Results of the macrophage uptake study showed that PEG5000-DSPE and PEG10000-DSPE coated groups with both high and low proportions (PEG-DSPE/PLGA 1:1, 0.25:1) could significantly reduce the phagocytosis of macrophages to microspheres compared with the uncoated PLGA group. For PEG2000-DSPE coated microspheres, the effect of escaping macrophage phagocytosis could be achieved by increasing the ratio of polyethylene glycol (PEG) on the surface of particles. Overall, the chain length of PEG-DSPE and its ratio are the key factors affecting the macrophage uptake. In pulmonary controlled drug delivery, high molecular weight of PEG-DSPE (PEG5000-DSPE and PEG10000-DSPE) and the high ratio (PEG-DSPE/PLGA 1:1) of PEG2000-DSPE can be selected to escape the phagocytosis of alveolar macrophages and prolong the drug retention in the lungs.

drug delivery system  /  inhalation  /  polyethylene glycol-distearoylphosphatidylethanolamine  /  polylactic acid-polyglycolic acid copolymer  /  phagocytosis
Jia-qi LI, Lu QIN, Huang-liang ZHENG, Xiao-ran LI, MICHAEL Moehwald, Lin CHEN, Yu-yang ZHANG, Shi-rui MAO. PEGylated phospholipid-coated polylactic acid-glycolic acid microspheres to escape the phagocytosis of alveolar macrophages[J]. Acta Pharmaceutica Sinica, 2019 , 54 (7) : 1303 -1311 . DOI: 10.16438/j.0513-4870.2019-0342
Year 2019 volume 54 Issue 7
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Article Info
doi: 10.16438/j.0513-4870.2019-0342
  • Receive Date:2019-04-29
  • Online Date:2026-01-26
  • Published:2019-07-12
Article Data
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History
  • Received:2019-04-29
  • Revised:2019-05-13
Funding
Affiliations
    1. School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China
    2. School of Life Sciences and Biological Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China
    3. Chemical and Pharmaceutical Development, Bayer AG D-42117, Germany
    4. Chemical and Pharmaceutical Development, Bayer AG, Beijing 100020, 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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