刘春雨, 付涛涛, 杨飞飞, 冯育林, 高红伟, 杨世林, 廖永红. 白头翁皂苷B4经气管和静脉给药后的肺部药代动力学与抗炎作用比较研究J. 药学学报, 2022, 57(9): 2791-2797. DOI: 10.16438/j.0513-4870.2022-0307
引用本文: 刘春雨, 付涛涛, 杨飞飞, 冯育林, 高红伟, 杨世林, 廖永红. 白头翁皂苷B4经气管和静脉给药后的肺部药代动力学与抗炎作用比较研究J. 药学学报, 2022, 57(9): 2791-2797. DOI: 10.16438/j.0513-4870.2022-0307
LIU Chun-yu, FU Tao-tao, YANG Fei-fei, FENG Yu-lin, GAO Hong-wei, YANG Shi-lin, LIAO Yong-hong. The pulmonary pharmacokinetics and anti-inflammatory effect of anemoside B4 after intratracheal and intravenous administrationJ. Acta Pharmaceutica Sinica, 2022, 57(9): 2791-2797. DOI: 10.16438/j.0513-4870.2022-0307
Citation: LIU Chun-yu, FU Tao-tao, YANG Fei-fei, FENG Yu-lin, GAO Hong-wei, YANG Shi-lin, LIAO Yong-hong. The pulmonary pharmacokinetics and anti-inflammatory effect of anemoside B4 after intratracheal and intravenous administrationJ. Acta Pharmaceutica Sinica, 2022, 57(9): 2791-2797. DOI: 10.16438/j.0513-4870.2022-0307

白头翁皂苷B4经气管和静脉给药后的肺部药代动力学与抗炎作用比较研究

The pulmonary pharmacokinetics and anti-inflammatory effect of anemoside B4 after intratracheal and intravenous administration

  • 摘要: 白头翁皂苷B4 (anemoside B4, B4) 是清热解毒中药白头翁的主要抗炎活性成分, 具有治疗肺部炎症的潜力。本文通过比较研究B4经气管和静脉给药后的肺部药代动力学与抗炎作用, 评价了B4经肺部给药的可行性。所有动物实验经中国医学科学院药用植物研究所伦理委员会批准(批准号: SLXD-20181113046)。体外气溶胶液滴粒径分布及其空气动力学特性评价结果显示, B4溶液经商品化雾化器雾化后形成的气溶胶具有良好的肺部沉积性能。药代动力学研究结果表明, B4经全身给药后药物肺组织渗透性差, 而经肺部给药后可以在肺内充分滞留, 肺组织局部生物利用度是静脉给药的1 000倍以上, 且药物在肺部的抗炎药物浓度可维持长达48 h。脂多糖(LPS) 诱导小鼠肺损伤模型的抗炎结果显示, B4经气管给药后的肺部抗炎作用具有剂量依赖性, 其最大抗炎强度强于10倍剂量静脉给药效果, 肺部给药后抗炎作用持续至少24 h。总体而言, 吸入给药是B4治疗肺部炎症的理想给药途径。

     

    Abstract: Anemoside B4 (B4), a main triterpenoid saponin from a traditional Chinese medicine plant, Pulsatilla chinensis, is a novel anti-inflammatory agent for protection from acute lung injury. We investigated the pulmonary availability and anti-inflammatory efficacy of B4 after intratracheal and intravenous dosing with a view to evaluating the suitability of inhalation delivery. All animal studies were performed under the guidelines approved by the Animal Care and Use Committee of Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences (Approval No: SLXD-20181113046). In vitro evaluation of the aerodynamic characteristics and droplet size distribution showed that the aerosols generated by a commercially available nebulizer were well deposited in the respiratory tract. Following intratracheal administration, B4 underwent pulmonary absorption into the bloodstream, rendering an absolute bioavailability of 103%. Compared to intravenous delivery, intratracheal administration dramatically increased the drug availability in lung tissue of rats by more than 1 000-fold, leading to improved and prolonged concentrations of B4 in lung tissue up to 48 h. In addition, the intratracheal administration of B4 resulted in dose-dependent and prolonged anti-inflammatory efficacy in a lipopolysaccharide (LPS)-induced lung injury model in mice. The present results demonstrate that inhalation delivery of B4 is a promising approach to treat pulmonary inflammation with once-daily dosing.

     

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