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用于瓣膜并发症的先进聚合基质。

Advanced polymeric matrix for valvular complications.

机构信息

Division of Pharmaceutical Sciences, School of Pharmacy, University of Missouri-Kansas City, Kansas City, Missouri 64108, USA.

出版信息

J Biomed Mater Res A. 2012 May;100(5):1151-9. doi: 10.1002/jbm.a.34055. Epub 2012 Feb 15.

DOI:10.1002/jbm.a.34055
PMID:22337643
Abstract

Poly(L-lactic acid) (PLLA) matrix systems incorporated with poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) containing nitric oxide (NO) donors (DETA NONOate) were developed for prevention of heart valve complications through sustained and controlled release of NO. PLLA matrices were prepared using the salt leaching method and the properties and drug release profiles were characterized. For assessment of the effects of PLLA systems on the pharmacological responses and cytotoxicity, various factors, such as calcium content, alkaline phosphatase (ALP) activity, cyclic guanosine monophosphate (cGMP) expression, intercellular adhesion molecule (ICAM-1) expression and cell viability of porcine aortic valve interstitial cells (PAVICs), were evaluated. PLLA matrices embedded with PLGA- NPs demonstrated its usefulness in alleviating the calcification rate of the VICs. The cGMP levels under osteoblastic conditions significantly increased, supporting that anticalcification activity of NO is mediated through NO-cGMP signaling pathway. The level of ICAM-1 expression in cells exposed to NO was lowered, suggesting that NO has an inhibitory activity against tissue inflammation. NO releases from PLLA matrix embedded with PLGA NPs prevented valvular calcification and inflammation without causing any cytotoxic activities. PLLA matrix system loaded with NPs containing NO donors could provide a new platform for sustained and controlled delivery of NO, significantly reducing valvular complications.

摘要

聚(L-丙交酯)(PLLA)基质系统与含有一氧化氮(NO)供体(DETA NONOate)的聚(乳酸-共-乙醇酸)(PLGA)纳米颗粒(NPs)结合,通过持续和控制NO 的释放来预防心脏瓣膜并发症。PLLA 基质采用盐溶法制备,并对其性能和药物释放曲线进行了表征。为了评估 PLLA 系统对药理反应和细胞毒性的影响,评估了各种因素,如钙含量、碱性磷酸酶(ALP)活性、环鸟苷酸(cGMP)表达、细胞间黏附分子(ICAM-1)表达和猪主动脉瓣间质细胞(PAVICs)的细胞活力。PLGA-NPs 嵌入的 PLLA 基质证明了其在减轻 VIC 钙化率方面的有用性。成骨条件下的 cGMP 水平显著升高,支持 NO 的抗钙化活性是通过 NO-cGMP 信号通路介导的。暴露于 NO 的细胞中 ICAM-1 表达水平降低,表明 NO 对组织炎症具有抑制活性。PLGA NPs 嵌入的 PLLA 基质中释放的 NO 可防止瓣膜钙化和炎症,而不会产生任何细胞毒性作用。载有 NO 供体的 NPs 的 PLLA 基质系统可为持续和控制 NO 释放提供新平台,显著降低瓣膜并发症的风险。

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