Chitosan/Alginate Nanoparticles with Sustained Release of Esculentoside A for Burn Wound Healing

被引:17
作者
Zhu, Zhikang [1 ,2 ,3 ]
He, Fang [1 ,2 ,3 ]
Shao, Huawei [1 ,2 ,3 ]
Shao, Jiaming [1 ,2 ,3 ]
Li, Qiong [1 ,2 ,3 ]
Ren, Haitao [1 ,2 ,3 ]
You, Chuangang [1 ,2 ,3 ]
Zhang, Zhongtao [1 ,2 ,3 ,4 ]
Han, Chunmao [1 ,2 ,3 ]
机构
[1] Zhejiang Univ Coll Med, Affiliated Hosp 2, Dept Burns & Wound Care Ctr, Hangzhou 310009, Peoples R China
[2] Zhejiang Univ, Coll Med, Hangzhou 310000, Peoples R China
[3] Key Lab Diag & Treatment Severe Trauma & Burn Zhej, Hangzhou 310009, Zhejiang, Peoples R China
[4] Affiliated Taian City Cent Hosp Qingdao Univ, Tumor Precise Intervent & Translat Med Lab, Tai An 271000, Peoples R China
基金
中国国家自然科学基金;
关键词
burn; dermal scaffolds; esculentoside A; inflammation; macrophage; CHITOSAN-ALGINATE NANOPARTICLES; IN-VITRO; REGENERATION; SCAFFOLDS; DELIVERY; MACROPHAGES; TRANSITION; PROTEIN; VIVO;
D O I
10.1021/acsanm.2c04714
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Burn injury remains one of the most devastating burdens on global public health. The inflammation, caused by burn injury and transplantation of dermal scaffolds, often leads to delayed burn wound healing. Esculentoside A (EsA), with a strong anti-inflammatory capacity, is an available agent that might contribute to the treatment of burn wounds. However, the poor stability and toxicity of EsA limit its clinical application. In the present study, we constructed chitosan/alginate nanoparticles (EsA-CS/ALG-NPs) to improve sustainability and reduce toxicity followed by impregnation of the prepared EsA-CS/ALG-NPs into a collagen/chitosan scaffold (EsA-CS/ALG-NPs@CCS). The particle size, structural morphology, thermal properties, and chemical interaction of repaired nanoparticles were evaluated using the Nanometrics instrument, differential scanning calorimetry, transmission electron microscopy, and Fourier transform infrared spectroscopy, respectively. The hybrid EsA-CS/ALG-NPs@CCS was evaluated for physical characteristics, in vitro drug release, biocompatibility, and anti-inflammation capacity with RAW 264.7 cells and in vivo burn wound healing studies with SD rats. The results showed that we successfully constructed CS/ALG-NPs and optimized the preparation process to achieve the highest encapsulation efficiency. The hybrid EsA-CS/ALG-NPs@CCS, with reduced cytotoxicity and sustained release of EsA, could alleviate inflammation, decrease the ratio of M1 macrophages, and increase the proportion of M2 macrophages in vitro. It was demonstrated that 5 mu g EsA CS/ALG-NPs@CCS not only reduces inflammatory cytokines secretion and inhibits M1 macrophages but also promotes the release of anti-inflammatory cytokines and activates M2 macrophages, thereby achieving accelerated and high quality healing of burn wounds ultimately. In summary, our work suggests that the synergistic combination of EsA, nanoparticles, and scaffolds provided a promising strategy for treating burn injuries.
引用
收藏
页码:573 / 587
页数:15
相关论文
共 54 条
[1]   Evaluation of biocompatibility and antioxidant efficiency of chitosan-alginate nanoparticles loaded with quercetin [J].
Aluani, Denitsa ;
Tzankova, Virginia ;
Kondeva-Burdina, Magdalena ;
Yordanov, Yordan ;
Nikolova, Elena ;
Odzhakov, Feodor ;
Apostolov, Alexandar ;
Markova, Tzvetanka ;
Yoncheva, Krassimira .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2017, 103 :771-782
[2]   bFGF and collagen matrix hydrogel attenuates burn wound inflammation through activation of ERK and TRK pathway [J].
Chakrabarti, Srijita ;
Mazumder, Bhaskar ;
Rajkonwar, Jadab ;
Pathak, Manash Pratim ;
Patowary, Pompy ;
Chattopadhyay, Pronobesh .
SCIENTIFIC REPORTS, 2021, 11 (01)
[3]   Esculentoside A inhibits LPS-induced acute kidney injury by activating PPAR-γ [J].
Chen, De-zhun ;
Chen, Li-qiong ;
Lin, Meng-xiang ;
Gong, Yu-qiang ;
Ying, Bin-yu ;
Wei, Da-zhen .
MICROBIAL PATHOGENESIS, 2017, 110 :208-213
[4]   Age-Related Alterations of Hyaluronan and Collagen in Extracellular Matrix of the Muscle Spindles [J].
Fan, Chenglei ;
Pirri, Carmelo ;
Fede, Caterina ;
Guidolin, Diego ;
Biz, Carlo ;
Petrelli, Lucia ;
Porzionato, Andrea ;
Macchi, Veronica ;
De Caro, Raffaele ;
Stecco, Carla .
JOURNAL OF CLINICAL MEDICINE, 2022, 11 (01)
[5]   Characterization and Mathematical Modeling of Alginate/Chitosan-Based Nanoparticles Releasing the Chemokine CXCL12 to Attract Glioblastoma Cells [J].
Gascon, Suzanne ;
Solano, Angela Giraldo ;
El Kheir, Wiam ;
Therriault, Helene ;
Berthelin, Pierre ;
Cattier, Bettina ;
Marcos, Bernard ;
Virgilio, Nick ;
Paquette, Benoit ;
Faucheux, Nathalie ;
Lauzon, Marc-Antoine .
PHARMACEUTICS, 2020, 12 (04)
[6]   Synthesis of Novel Derivatives of Esculentoside A and Its Aglycone Phytolaccagenin, and Evaluation of Their Haemolytic Activity and Inhibition of Lipopolysaccharide-Induced Nitric Oxide Production [J].
Gong, Wei ;
Jiang, Zhihui ;
Sun, Peng ;
Li, Ling ;
Jin, Yongsheng ;
Shao, Lucheng ;
Zhang, Wen ;
Liu, Baoshu ;
Zhang, Hongwei ;
Tang, Hua ;
Chen, Yufeng ;
Yi, Yanghua ;
Zhang, Dazhi .
CHEMISTRY & BIODIVERSITY, 2011, 8 (10) :1833-1852
[7]   Determination of esculentoside A in dog plasma by LC-MS/MS method: Application to pre-clinical pharmacokinetics [J].
Guan, Xiaoduo ;
Chang, Huichao ;
Sun, Fanlu ;
Chen, Xiaohui ;
Zhang, Wen ;
Fan, Guorong .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2013, 72 :261-266
[8]   α-Lactalbumin-Based Nanofiber Dressings Improve Burn Wound Healing and Reduce Scarring [J].
Guo, Xiong ;
Liu, Yunen ;
Bera, Hriday ;
Zhang, Haotian ;
Chen, Yang ;
Cun, Dongmei ;
Fodera, Vito ;
Yang, Mingshi .
ACS APPLIED MATERIALS & INTERFACES, 2020, 12 (41) :45702-45713
[9]   Integrating non-targeted metabolomics and toxicology networks to study the mechanism of Esculentoside A-induced hepatotoxicity in rats [J].
He, Tao ;
Liu, Chuanxin ;
Li, Mengyu ;
Wang, Mingshuang ;
Liu, Ning ;
Zhang, Dan ;
Han, Shuang ;
Li, Wenxian ;
Chen, Shilin ;
Yuan, Ruijuan ;
Huang, Jianmei .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2021, 35 (06) :1-15
[10]   Esculentoside A alleviates cognitive deficits and amyloid pathology through peroxisome proliferator-activated receptor γ-dependent mechanism in an Alzheimer's disease model [J].
He, Zhijun ;
Li, Xiaoqian ;
Wang, Zi ;
Tu, Sixin ;
Feng, Jiale ;
Du, Xiubo ;
Ni, Jiazuan ;
Li, Nan ;
Liu, Qiong .
PHYTOMEDICINE, 2022, 98