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Preparation of apigenin β-cyclodextrin inclusion complexe DPPC liposomal dry powder inhalers and the effect on acute severe pneumonia
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Li-fei ZHU, Si-qi ZHANG, Ting-ting WU, Hong-jun CHEN, Yan HUO*
Acta Pharmaceutica Sinica | 2026, 61(6) : 2257 - 2265
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Acta Pharmaceutica Sinica | 2026, 61(6): 2257-2265
• Original Articles •
Preparation of apigenin β-cyclodextrin inclusion complexe DPPC liposomal dry powder inhalers and the effect on acute severe pneumonia
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Li-fei ZHU, Si-qi ZHANG, Ting-ting WU, Hong-jun CHEN, Yan HUO*
Affiliations
  • Department of Pharmacy, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China
Published: 2026-06-12 doi: 10.16438/j.0513-4870.2025-0407
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To identify a new treatment strategy for acute severe pneumonia and solve the bioavailability of apigenin in formulation, the research utilized dipalmitoylphosphatidylcholine (DPPC), as well as 2-hydroxypropyl-β-cyclodextrin as respiratory carriers, to develop the apigenin β-cyclodextrin inclusion complexe DPPC liposomal dry powder inhalers (ACDLDPIs). The ACDLDPIs were prepared by grinding, film-dispersion and freeze drying. The formulation was optimized by orthogonal design, and its particle size, entrapment efficiency, electric potential, in vitro release and lung deposition were studied. Lipopolysaccharide (LPS)-induced rat acute lung injury model was used to evaluate acute severe pneumonia in vivo. The optimal formulation for apigenin cyclodextrin inclusion was obtained with the mole ratio of apigenin/cyclodextrin as (2∶1), concentration of cyclodextrin as 20% and grinding time as 90 min. The optimized prescription of the ACDLDPIs was apigenin inclusion complex/DPPC (1∶2), 15 min hydration time and the mass ratio of mannitol/DPPC (1∶1). Its encapsulation efficiency was (71.46 ± 3.18)%, and the drug loading was (8.36 ± 0.42)%. The particle size was 198.6 ± 4.4 nm (before rehydration) and 221.6 ± 5.5 nm (after rehydration). The zeta potential was 15.3 ± 2.1 mV. The aerodynamic particle size was 4.28 ± 0.77 μm. The pulmonary deposition rate (FPF) was 43.02%. The experiment was approved by the Experimental Animal Ethics Committee of Tongji University Affiliated Yangpu Hospital (No: LL-2023-ZRKX-002). The pharmacodynamic evaluation of acute severe pneumonia was evaluated in vivo. ACDLDPIs group had better therapeutic effect than apigenin group. The ACDLDPIs had suitable particle size, uniform distribution, good stability, high lung deposition rate and good therapeutic effect on acute severe pneumonia in vivo. The ACDLDPIs are promising medicines for the treatment of acute severe pneumonia.

apigenin  /  dipalmitoylphosphatidylcholine  /  cyclodextrin  /  dry powder inhalation  /  acute severe pneumonia
朱李飞, 张思棋, 吴婷婷, 陈红君, 霍炎. 芹菜素包合物二棕榈酰卵磷脂脂质干粉吸入剂的制备及其治疗急性重症肺炎作用研究. 药学学报, 2026 , 61 (6) : 2257 -2265 . DOI: 10.16438/j.0513-4870.2025-0407
Li-fei ZHU, Si-qi ZHANG, Ting-ting WU, Hong-jun CHEN, Yan HUO. Preparation of apigenin β-cyclodextrin inclusion complexe DPPC liposomal dry powder inhalers and the effect on acute severe pneumonia[J]. Acta Pharmaceutica Sinica, 2026 , 61 (6) : 2257 -2265 . DOI: 10.16438/j.0513-4870.2025-0407
Year 2026 volume 61 Issue 6
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Article Info
doi: 10.16438/j.0513-4870.2025-0407
  • Receive Date:2025-03-06
  • Online Date:2026-09-21
  • Published:2026-06-12
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  • Received:2025-03-06
  • Revised:2025-08-19
Affiliations
    Department of Pharmacy, Yangpu Hospital, Tongji University School of Medicine, Shanghai 200090, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
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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