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用于创伤后止血和组织修复的家蚕茧衍生碳点

Silkworm Cocoon-Derived Carbon Dots for Post-Trauma Hemostasis and Tissue Repair.

作者信息

Wu Xinru, Yao Miaomiao, Qiao Xuan, Li Lintao, Meng Zhiyun, Liu Shuchen, Sun Yunbo, Gan Hui, Zhu Xiaoxia, Wu Zhuona, Gu Ruolan, Dou Guifang

机构信息

Beijing Institute of Radiation Medicine, Beijing 100850, China.

School of Pharmaceutical Sciences, Anhui Medical University, Hefei 230032, China.

出版信息

Pharmaceuticals (Basel). 2025 Apr 22;18(5):603. doi: 10.3390/ph18050603.

DOI:10.3390/ph18050603
PMID:40430424
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12114995/
Abstract

Traumatic hemorrhage management is challenging due to the need to control severe bleeding and support tissue repair. An ideal material would possess both hemostatic and wound-healing properties. Silkworm cocoon-derived carbon dots (SC-CDs) were synthesized via a hydrothermal method. After physical and chemical characterization using techniques such as HR-TEM and XPS, their hemostatic efficacy was assessed in rat liver injury, tail transection, and mouse coagulation disorder models. Moreover, the effects of the SC-CDs on platelet aggregation and activation were evaluated. The potential of the SC-CDs to promote wound healing was investigated through cell scratch assays and a mouse full-thickness skin defect model. The SC-CDs showed a high quantum yield (12.9% ± 0.42%), with low hemolytic activity and cytotoxicity. In the hemostasis models, the SC-CDs significantly reduced the bleeding time and volume. In the rat liver injury model, the bleeding time was shortened from 152.67 ± 4.16 s (Control) to 55.33 ± 9.50 s ( < 0.05). In the rat tail transection model, the bleeding volume was reduced from 1.71 ± 0.16 g (Control) to 0.4 ± 0.11 g ( < 0.05). In the mouse coagulation disorder model, an 8 mg/kg dose reduced the bleeding volume to 11.80% ± 0.39% of that of the Control ( < 0.05). Mechanistic studies suggested enhanced platelet activation and aggregation. In the wound healing experiments, the SC-CDs reduced the wound area (88.53 ± 11.78 mm (Control) vs. 70.07 ± 6.71 mm (SC-CDs), < 0.05) and promoted fibroblast migration (24 h scratch width: 372.34 ± 9.06 μm (Control) vs. 259.49 ± 36.75 μm (SC-CDs), < 0.05). SC-CDs show promise for hemorrhage management and tissue regeneration, with potential applications in cases of internal bleeding or coagulation disorders.

摘要

由于需要控制严重出血并支持组织修复,创伤性出血的管理具有挑战性。理想的材料应兼具止血和伤口愈合特性。通过水热法合成了家蚕茧衍生的碳点(SC-CDs)。使用高分辨透射电子显微镜(HR-TEM)和X射线光电子能谱(XPS)等技术进行物理和化学表征后,在大鼠肝损伤、尾部横断和小鼠凝血障碍模型中评估了它们的止血效果。此外,还评估了SC-CDs对血小板聚集和激活的影响。通过细胞划痕试验和小鼠全层皮肤缺损模型研究了SC-CDs促进伤口愈合的潜力。SC-CDs显示出高量子产率(12.9%±0.42%),溶血活性和细胞毒性较低。在止血模型中,SC-CDs显著缩短了出血时间和减少了出血量。在大鼠肝损伤模型中,出血时间从152.67±4.16秒(对照组)缩短至55.33±9.50秒(P<0.05)。在大鼠尾部横断模型中,出血量从1.71±0.16克(对照组)减少至0.4±0.11克(P<0.05)。在小鼠凝血障碍模型中,8毫克/千克剂量将出血量减少至对照组的11.80%±0.39%(P<0.05)。机制研究表明血小板激活和聚集增强。在伤口愈合实验中,SC-CDs减小了伤口面积(对照组88.53±11.78平方毫米 vs. SC-CDs组70.07±6.71平方毫米,P<0.05)并促进了成纤维细胞迁移(24小时划痕宽度:对照组372.34±9.06微米 vs. SC-CDs组259.49±36.75微米,P<0.05)。SC-CDs在出血管理和组织再生方面显示出前景,在内部出血或凝血障碍病例中具有潜在应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/7385c71f6c76/pharmaceuticals-18-00603-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/cb219a1404cf/pharmaceuticals-18-00603-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/db9c86bfbd34/pharmaceuticals-18-00603-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/707a42e10558/pharmaceuticals-18-00603-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/8f5aa874a82c/pharmaceuticals-18-00603-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/edec90114269/pharmaceuticals-18-00603-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/7385c71f6c76/pharmaceuticals-18-00603-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/cb219a1404cf/pharmaceuticals-18-00603-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/db9c86bfbd34/pharmaceuticals-18-00603-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/707a42e10558/pharmaceuticals-18-00603-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/8f5aa874a82c/pharmaceuticals-18-00603-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/edec90114269/pharmaceuticals-18-00603-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c691/12114995/7385c71f6c76/pharmaceuticals-18-00603-g006.jpg

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