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Cepharanthine loaded nanoparticles coated with macrophage membranes for lung inflammation therapy.
Lu, Caihong; Zheng, Jinpeng; Ding, Yaning; Meng, Yuanyuan; Tan, Fangyun; Gong, Wei; Chu, Xiaoyang; Kong, Xiaolong; Gao, Chunsheng.
Affiliation
  • Lu C; School of Pharmacy, Guangxi Medical University, Nanning, P. R. China.
  • Zheng J; State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, Beijing, P. R. China.
  • Ding Y; State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, Beijing, P. R. China.
  • Meng Y; School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang, P. R. China.
  • Tan F; School of Pharmacy, Guangxi Medical University, Nanning, P. R. China.
  • Gong W; School of Pharmacy, Guangxi Medical University, Nanning, P. R. China.
  • Chu X; State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and Toxicology, Beijing, P. R. China.
  • Kong X; Department of Stomatology, The Fifth Medical Center of PLA General Hospital, Beijing, P. R. China.
  • Gao C; School of Pharmacy, Guangxi Medical University, Nanning, P. R. China.
Drug Deliv ; 28(1): 2582-2593, 2021 Dec.
Article in En | MEDLINE | ID: mdl-34866533
ABSTRACT
Acute lung injury (ALI) is a disease associated with suffering and high lethality, but to date without any effective pharmacological management in the clinic. In the pathological mechanisms of ALI, a strong inflammatory response plays an important role. Herein, based on macrophage 'homing' into inflammation sites and cell membrane coating nanotechnology, we developed a biomimetic anti-inflammation nanosystem (MM-CEP/NLCs) for the treatment of ALI. MM-CEP/NLCs were made with nanostructured lipid carriers (NLCs) coated with natural macrophage membranes (MMs) to achieve effective accumulation of cepharanthine (CEP) in lung inflammation to achieve the effect of treating ALI. With the advantage of suitable physicochemical properties of NLCs and unique biological functions of the macrophage membrane, MM-CEP/NLCs were stabilized and enabled sustained drug release, providing improved biocompatibility and long-term circulation. In vivo, the macrophage membranes enabled NLCs to be targeted and accumulated in the inflammation sites. Further, MM-CEP/NLCs significantly attenuated the severity of ALI, including lung water content, histopathology, bronchioalveolar lavage cellularity, protein concentration, and inflammation cytokines. Our results provide a bionic strategy via the biological properties of macrophages, which may have greater value and application prospects in the treatment of inflammation.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia / Benzylisoquinolines / Nanoparticles / Macrophages Type of study: Clinical_trials Limits: Animals / Humans / Male Language: En Journal: Drug Deliv Journal subject: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia / Benzylisoquinolines / Nanoparticles / Macrophages Type of study: Clinical_trials Limits: Animals / Humans / Male Language: En Journal: Drug Deliv Journal subject: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Year: 2021 Document type: Article