Porous gelatin microspheres for controlled drug delivery with high hemostatic efficacy

明胶 止血 扫描电子显微镜 肿胀 的 止血剂 药物输送 生物医学工程 体内 傅里叶变换红外光谱 材料科学 多孔性 化学 色谱法 控制释放 化学工程 纳米技术 医学 外科 复合材料 生物化学 有机化学 生物技术 工程类 生物
作者
Shuang Cao,Lin Li,Yan Du,Jufen Gan,Jing Wang,Tao Wang,Ying Liu,Wei Liu,Yejin Zhou,Xin Gao,Hong Li,Tielong Liu
出处
期刊:Colloids and Surfaces B: Biointerfaces [Elsevier BV]
卷期号:207: 112013-112013 被引量:33
标识
DOI:10.1016/j.colsurfb.2021.112013
摘要

Effective hemostasis and antibacterial efficacy for extensive trauma in a warzone and civilian accidents are important for reducing mortalities and serious complications. Gelatin has been widely used as a hemostatic agent and has the potential for use in drug delivery systems. To enhance its hemostatic efficiency and create conducive conditions for sustained drug release, we developed Vancomycin-impregnated porous gelatin microspheres (Van-MS) by introducing the porous structure into gelatin. Results showed that Van-MS can be successfully developed via the ice crystal pore-making method combined with hydration maintaining its stability. We also explored the use of biodegradable porous materials for treatment of infections and bleeding in soft tissue, and analyzed Van-MS via scanning electron microscopy (SEM), scanning electron microscopy and energy dispersive X-ray spectrometry (SEM-EDS), Fourier Transform infrared spectroscopy (FTIR) and High-Performance Liquid Chromatography (HPLC). Results from Van-MS showed high hemostatic both efficacies in vivo and in vitro. Moreover, muscle lesions treated by Van-MS showed formation of fibrous connective tissue and were nearly sealed after 10 days in a rabbit traumatic infection model. This antibacterial performance was attributed to absorption of exudates and sustained drug release. Hemostatic effects were due to: (1) particles water swelling form a physical barrier that led to physical hemostasis; (2) activation of the endogenous coagulation pathway which resulted in physiological hemostasis; (3) aggregation of platelets and erythrocytes after absorbing water; and (4) stronger hemostatic properties owing to their porous structure with high specific surface area.
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