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可吸入穿心莲内酯-β-环糊精包合物通过调节免疫反应治疗金黄色葡萄球菌肺炎

Inhalable Andrographolide-β-cyclodextrin Inclusion Complexes for Treatment of Staphylococcus aureus Pneumonia by Regulating Immune Responses.

作者信息

Zhang Tongtong, Zhu Lifei, Li Miao, Hu Yuzhen, Zhang Erfeng, Jiang Qingcheng, Han Guang, Jin Yiguang

机构信息

Department of Graduates, Anhui Medical University , Hefei 230001, China.

Department of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine , Beijing 100850, China.

出版信息

Mol Pharm. 2017 May 1;14(5):1718-1725. doi: 10.1021/acs.molpharmaceut.6b01162. Epub 2017 Apr 5.

Abstract

Bacterial pneumonia is a serious disease with high mortality if no appropriate and immediate therapy is available. Andrographolide (AG) is an anti-inflammatory agent extracted from a traditional Chinese herb andrographis paniculata. Oral AG tablets and pills are clinically applied for treatment of upper respiratory tract infections. However, the low solubility and bioavailability of AG lead to high doses and long-term therapy. Here we developed an andrographolide-β-cyclodextrin inclusion complex (AG-β-CD) for inhalation therapy of Staphylococcus aureus pneumonia. AG-β-CD was identified with X-ray diffraction and FT-IR. Surprisingly, both AG-β-CD and AG showed little in vitro anti-S. aureus activity. However, pulmonary delivery of AG, AG-β-CD, or penicillin had significant anti-S. aureus pneumonia effects. Leukocytes, neutrophils, white blood cells, total proteins, TNF-α, IL-6, NF-κB p65 expression, and bacterial colonies in the bronchoalveolar lavage fluids were detected. Pulmonary delivery of AG and AG-β-CD led to bacterial inhibition and inflammation alleviation by regulating immune responses, while penicillin only killed bacteria without significant immune regulation. Moreover, the antipneumonia activity of AG-β-CD was much higher than that of AG, probably resulting from locally accelerated AG dissolution due to β-CD inclusion. The aerodynamic diameter of AG-β-CD powders was 2.03 μm, suitable for pulmonary delivery. Inhalable AG-β-CD is a promising antibacterial and anti-inflammatory medicine for the treatment of S. aureus pneumonia by regulating immune responses, and the effect is enhanced by β-CD inclusion. AG and its formulations might be potent weapons against the resistant bacterial pneumonia due to their specific mechanism in the future.

摘要

细菌性肺炎是一种严重疾病,若没有适当且及时的治疗,死亡率很高。穿心莲内酯(AG)是从传统中药穿心莲中提取的一种抗炎剂。口服AG片和丸剂在临床上用于治疗上呼吸道感染。然而,AG的低溶解度和生物利用度导致需要高剂量和长期治疗。在此,我们开发了一种用于吸入治疗金黄色葡萄球菌肺炎的穿心莲内酯-β-环糊精包合物(AG-β-CD)。通过X射线衍射和傅里叶变换红外光谱对AG-β-CD进行了鉴定。令人惊讶的是,AG-β-CD和AG在体外均显示出对金黄色葡萄球菌的微弱活性。然而,AG、AG-β-CD或青霉素的肺部给药对金黄色葡萄球菌肺炎具有显著疗效。检测了支气管肺泡灌洗液中的白细胞、中性粒细胞、白细胞总数、总蛋白、肿瘤坏死因子-α、白细胞介素-6、核因子-κB p65表达以及菌落。AG和AG-β-CD的肺部给药通过调节免疫反应导致细菌抑制和炎症减轻,而青霉素仅杀灭细菌,没有显著的免疫调节作用。此外,AG-β-CD的抗肺炎活性远高于AG,这可能是由于β-环糊精包合导致AG在局部加速溶解。AG-β-CD粉末的空气动力学直径为2.03μm,适合肺部给药。可吸入的AG-β-CD是一种有前景的抗菌和抗炎药物,通过调节免疫反应来治疗金黄色葡萄球菌肺炎,并且β-环糊精包合增强了其效果。由于其特定机制,AG及其制剂未来可能成为对抗耐药细菌性肺炎的有力武器。

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