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新型可生物降解胶水持续释放万古霉素以预防耐甲氧西林金黄色葡萄球菌移植感染。

Sustained release of vancomycin from a new biodegradable glue to prevent methicillin-resistant Staphylococcus aureus graft infection.

作者信息

Morishima Manabu, Marui Akira, Yanagi Shigeki, Nomura Takamasa, Nakajima Naoki, Hyon Suong-Hyu, Ikeda Tadashi, Sakata Ryuzo

机构信息

Department of Cardiovascular Surgery, Kyoto University Graduate School of Medicine, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.

出版信息

Interact Cardiovasc Thorac Surg. 2010 Jul;11(1):52-5. doi: 10.1510/icvts.2010.232447. Epub 2010 Apr 1.

DOI:10.1510/icvts.2010.232447
PMID:20360210
Abstract

Prosthetic graft infection with methicillin-resistant Staphylococcus aureus (MRSA) is one of the most serious complications of cardiovascular surgery. Seeking to prevent graft infection, we evaluated the efficacy of a new biodegradable hydrogel glue (new-glue) composed of aldehyded dextran and epsilon-poly(L-lysine) which acts as a local sustained-release carrier of vancomycin. Rats (n=40) were implanted with 1-cm(2) Dacron grafts in the subcutaneous pockets. Groups (n=10 each) were as follows: no treatment (group A), topical vancomycin solution (group B), new-glue without vancomycin (group C) or new-glue containing 1 mg of vancomycin (group D). Twenty-four h after the implantation, 2.0x10(7) colony-forming units of MRSA was inoculated onto the graft surface. Seven days thereafter, the graft was sampled and cultured. The quantity of MRSA was significantly lower in group D than in the other groups (P<0.0001). About 95% of the total vancomycin was released from the new-glue over the 72 h experimental period, and the tissue concentration of vancomycin remained above the minimum inhibitory concentration for the MRSA strain throughout the experiment. This new vancomycin-containing glue effectively prevented prosthetic graft infection and thus may be a promising biodegradable drug vehicle.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)所致的人工血管移植物感染是心血管手术最严重的并发症之一。为预防移植物感染,我们评估了一种新型可生物降解水凝胶胶水(新型胶水)的疗效,该胶水由醛化葡聚糖和ε-聚(L-赖氨酸)组成,可作为万古霉素的局部缓释载体。将大鼠(n = 40)在皮下囊袋植入1 cm²的涤纶移植物。分组(每组n = 10)如下:不治疗(A组)、局部应用万古霉素溶液(B组)、不含万古霉素的新型胶水(C组)或含1 mg万古霉素的新型胶水(D组)。植入后24小时,将2.0×10⁷个MRSA菌落形成单位接种到移植物表面。此后7天,对移植物进行取样培养。D组的MRSA数量显著低于其他组(P < 0.0001)。在72小时的实验期内,约95%的总万古霉素从新型胶水中释放出来,并且在整个实验过程中,万古霉素的组织浓度保持在高于MRSA菌株最低抑菌浓度的水平。这种新型含万古霉素胶水有效预防了人工血管移植物感染,因此可能是一种有前景的可生物降解药物载体。

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