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外周血血浆凝块作为局部抗菌药物递送基质。

Peripheral Blood Plasma Clot as a Local Antimicrobial Drug Delivery Matrix.

机构信息

1 Department of Trauma Surgery, BG University Hospital Bergmannsheil, Ruhr University Bochum , Bochum, Germany .

2 Department of Surgical Research, BG University Hospital Bergmannsheil, Ruhr University Bochum , Bochum, Germany .

出版信息

Tissue Eng Part A. 2018 May;24(9-10):809-818. doi: 10.1089/ten.TEA.2017.0319. Epub 2018 Jan 3.

Abstract

Platelet-free blood plasma clots were loaded either with antibiotics (vancomycin, gentamicin, or linezolid) at concentrations of 5-300 μg/mL or with silver ions (silver acetate) at concentrations of 3.3-129 μg/mL. The release of antibiotics or silver from the clot matrix was analyzed after repeated immersion of the plasma clots using reversed-phase high-performance liquid chromatography (RP-HPLC) or atomic absorption spectroscopy (AAS). The antimicrobial activity was tested against Staphylococcus aureus; tissue cell compatibility was analyzed using human mesenchymal stem cells (hMSC). Fibrin fiber thickness of the clots was analyzed by scanning electron microscopy. While addition of linezolid and vancomycin did not significantly change the fibrin fiber thickness, gentamicin and silver ions led to an increase in fiber thickness. All antibiotics showed a concentration-dependent burst-like release from the plasma clots within 1 h followed by a general decay in elution. The release of vancomycin and gentamicin, or silver lasted up to 7 days (depending on initial concentrations), but lasted only up to 4 h for linezolid. A correlation (p < 0.0001) was noted between the concentration of released antibiotics analyzed by HPLC and antimicrobial activity (agar diffusion test). A decrease in antibacterial activity of gentamicin- and vancomycin-containing clots occurred within 4 or 5 days. In contrast, the corresponding antibacterial activity of plasma clots containing linezolid was limited to 3 h. Antibacterial activity of plasma clots containing silver at the highest concentrations decreased after day 3, but clots with lower concentrations induced incomplete bacterial lysis or displayed no antibacterial activity. The antibiotic-containing clots did not induce cytotoxic effects on the embedded hMSC in contrast to all clots containing silver. Our results indicate that an autologous plasma clot can be used to deliver antibiotics such as vancomycin and gentamicin in combination with hMSC and the antibacterial effects persist for days without inducing cytotoxic effects on the embedded stem cells.

摘要

无细胞血浆血栓分别用浓度为 5-300μg/ml 的抗生素(万古霉素、庆大霉素或利奈唑胺)或浓度为 3.3-129μg/ml 的银离子(醋酸银)加载。使用反相高效液相色谱法(RP-HPLC)或原子吸收光谱法(AAS)分析血浆血栓反复浸泡后抗生素或银从血栓基质中的释放情况。采用金黄色葡萄球菌检测抗生素的抗菌活性;用人骨髓间充质干细胞(hMSC)分析组织细胞相容性。通过扫描电子显微镜分析血栓的纤维蛋白纤维厚度。虽然添加利奈唑胺和万古霉素不会显著改变纤维蛋白纤维厚度,但庆大霉素和银离子会导致纤维厚度增加。所有抗生素在 1 小时内均表现出浓度依赖性的爆发式释放,随后洗脱量普遍下降。万古霉素和庆大霉素或银的释放可持续长达 7 天(取决于初始浓度),而利奈唑胺仅可持续 4 小时。通过 HPLC 分析释放的抗生素浓度与抗菌活性(琼脂扩散试验)之间存在相关性(p<0.0001)。含庆大霉素和万古霉素的血栓的抗菌活性在 4 或 5 天内下降。相比之下,含有利奈唑胺的血浆血栓的相应抗菌活性仅限于 3 小时。含最高浓度银的血浆血栓的抗菌活性在第 3 天后下降,但浓度较低的血栓诱导不完全细菌裂解或无抗菌活性。与所有含银的血栓不同,含抗生素的血栓对嵌入的 hMSC 没有细胞毒性作用。我们的结果表明,自体血浆血栓可用于递送抗生素,如万古霉素和庆大霉素,与 hMSC 结合,并在数天内保持抗菌效果,而不会对嵌入的干细胞产生细胞毒性作用。

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