Suppr超能文献

生物可降解纳米粒增强药物递送的纳米优势:清除减少的贡献。

Nano-advantage in enhanced drug delivery with biodegradable nanoparticles: contribution of reduced clearance.

机构信息

Nanomedicine and Drug Delivery Laboratory, Department of Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, 12850 E. Montview Blvd., Aurora, CO 80045, USA.

出版信息

Drug Metab Dispos. 2012 Jul;40(7):1380-8. doi: 10.1124/dmd.112.044925. Epub 2012 Apr 12.

Abstract

The aim of this study was to investigate the contribution of reduced apparent clearance to the enhanced exposure reported for biodegradable nanoparticles after extravascular and intravascular routes of administration. Plasma concentration profiles for drug and nanoparticle formulations after administration by intravenous, intraduodenal, and oral routes were extracted from the literature. Data were fit to pharmacokinetic models using BOOMER. The compartmental pharmacokinetic analysis of literature data for six drugs (camptothecin, 9-nitrocamptothecin, epirubicin, vinpocetine, clozapine, and cyclosporine) showed that the encapsulation of drug molecules in nanoparticles significantly reduced the apparent clearance and prolonged the apparent circulation half-life compared with those for the plain drug. Positively charged nanoparticles assessed in this study had lower apparent clearance, lower elimination rate constant values, and longer apparent circulation half-life than neutral and negatively charged nanoparticles. After oral administration, a reduction in apparent clearance contributed substantially to elevations in plasma drug exposure with nanoparticles. For the drugs and delivery systems examined, the nano-advantage in drug delivery enhancement can be explained, in part, by reduced clearance.

摘要

本研究旨在探讨在血管内外给药途径后,可生物降解纳米颗粒的增强暴露报道中,表观清除率降低的贡献。从文献中提取了药物和纳米颗粒制剂在静脉内、十二指肠内和口服给药后的血浆浓度曲线。使用 BOOMER 对文献中六种药物(喜树碱、9-硝基喜树碱、表阿霉素、长春西汀、氯氮平和环孢素)的数据进行了房室药代动力学分析,结果表明与普通药物相比,药物分子被纳米颗粒包封显著降低了表观清除率并延长了表观循环半衰期。本研究评估的带正电荷的纳米颗粒的表观清除率较低、消除速率常数值较低、表观循环半衰期较长,与中性和带负电荷的纳米颗粒相比。口服给药后,纳米颗粒的表观清除率降低导致血浆药物暴露显著升高。对于所研究的药物和给药系统,部分可以通过降低清除率来解释纳米药物递送增强的优势。

相似文献

6
Targeting of injectable drug nanocrystals.可注射药物纳米晶体的靶向性
Mol Pharm. 2014 Jun 2;11(6):1762-71. doi: 10.1021/mp5001247. Epub 2014 Apr 25.
10
Nanocarriers for oral drug delivery.纳米载体用于口服药物递送。
J Drug Target. 2013 Jul;21(6):515-27. doi: 10.3109/1061186X.2013.789033. Epub 2013 Apr 26.

引用本文的文献

本文引用的文献

1
Nanoparticle uptake by the oral route: Fulfilling its potential?纳米颗粒的口服摄取:能否发挥其潜力?
Drug Discov Today Technol. 2005 Spring;2(1):75-81. doi: 10.1016/j.ddtec.2005.05.019.
4
Strategies in the design of nanoparticles for therapeutic applications.用于治疗应用的纳米粒子设计策略。
Nat Rev Drug Discov. 2010 Aug;9(8):615-27. doi: 10.1038/nrd2591. Epub 2010 Jul 9.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验