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本文引用的文献

1
Hybrid Integrated Silicon Microfluidic Platform for Fluorescence Based Biodetection.用于基于荧光的生物检测的混合集成硅微流控平台
Sensors (Basel). 2007 Sep 11;7(9):1901-1915. doi: 10.3390/s7091901.
2
Controllable microfluidic synthesis of multiphase drug-carrying lipospheres for site-targeted therapy.用于靶向治疗的多相载药脂质球的可控微流体制备
Biotechnol Prog. 2009 Jul-Aug;25(4):938-45. doi: 10.1002/btpr.214.
3
Novel preparation techniques for controlling microbubble uniformity: a comparison.新型制备技术控制微泡均匀性的比较。
Med Biol Eng Comput. 2009 Aug;47(8):883-92. doi: 10.1007/s11517-009-0490-8. Epub 2009 May 12.
4
Microfluidic preparation of monodisperse ethyl cellulose hollow microcapsules with non-toxic solvent.使用无毒溶剂通过微流体制备单分散乙基纤维素空心微胶囊
J Colloid Interface Sci. 2009 Aug 1;336(1):100-6. doi: 10.1016/j.jcis.2009.03.050. Epub 2009 Apr 5.
5
A microfluidic approach to chemically driven assembly of colloidal particles at gas-liquid interfaces.一种在气液界面通过化学驱动实现胶体颗粒组装的微流控方法。
Angew Chem Int Ed Engl. 2009;48(29):5300-4. doi: 10.1002/anie.200805204.
6
Microbubble size isolation by differential centrifugation.通过差速离心法分离微泡大小
J Colloid Interface Sci. 2009 Jan 15;329(2):316-24. doi: 10.1016/j.jcis.2008.09.066. Epub 2008 Oct 1.
7
Microfluidic fabrication of monodisperse biocompatible and biodegradable polymersomes with controlled permeability.具有可控渗透性的单分散生物相容性和可生物降解聚合物囊泡的微流体制备。
J Am Chem Soc. 2008 Jul 23;130(29):9543-9. doi: 10.1021/ja802157y. Epub 2008 Jun 25.
8
Ultrasound microbubble contrast agents: fundamentals and application to gene and drug delivery.超声微泡造影剂:基本原理及其在基因和药物递送中的应用
Annu Rev Biomed Eng. 2007;9:415-47. doi: 10.1146/annurev.bioeng.8.061505.095852.
9
Multiphase flow in microfluidic systems --control and applications of droplets and interfaces.微流控系统中的多相流——液滴与界面的控制及应用
Adv Colloid Interface Sci. 2007 May 31;133(1):35-49. doi: 10.1016/j.cis.2007.03.001. Epub 2007 Mar 16.
10
On-chip generation of microbubbles as a practical technology for manufacturing contrast agents for ultrasonic imaging.作为制造超声成像造影剂的实用技术的微泡片上生成。
Lab Chip. 2007 Apr;7(4):463-8. doi: 10.1039/b701481n. Epub 2007 Mar 8.

聚合物-脂质微泡用于生物传感和多孔结构的形成。

Polymer-lipid microbubbles for biosensing and the formation of porous structures.

机构信息

Department of Biomedical Engineering, University of California at Irvine, Irvine, CA 92697, USA.

出版信息

J Colloid Interface Sci. 2010 Apr 15;344(2):521-7. doi: 10.1016/j.jcis.2010.01.042. Epub 2010 Jan 18.

DOI:10.1016/j.jcis.2010.01.042
PMID:20163798
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2949358/
Abstract

Polymer-lipid microbubbles (PLBs) are generated by microfluidic flow-focusing devices to form a new class of long-lasting hybrid particles. The specific PLB construct developed is an elastic gas-filled microsphere with a polydimethylsiloxane (PDMS) shell containing phospholipids conjugated to functionalized polyethyleneglycol (PEG). Digital "droplet-based" microfluidics technology enables control of particle composition, size, and polydispersity (sigma<10%). Use of PDMS as a shell component improves the functionality and stability (lifetime>6 months) of the hybrid particles due to the thermally maneuverable solidification process. With a gas core, they serve as a template material for creating three-dimensional porous structures and surfaces, requiring no cumbersome post-processing removal steps. By adding biotinylated PEG-lipid derivatives that offer targeting capabilities, we demonstrate the immobilization of fluorescent IgG antibodies on stationary PDMS-lipid microbubbles through biotin-avidin interactions and on-chip trapping for immunoassays. A PDMS-lipid composition offers several advantages such as biocompatibility and biodegradability for future in vivo use as porous engineered scaffolds, packing materials, or delivery (e.g. therapeutic) agents with cell targeting capability.

摘要

聚合物-脂质微泡(PLB)是通过微流控流聚焦装置产生的,形成了一类新的长寿命混合颗粒。所开发的特定 PLB 结构是一种弹性充气微球,具有包含与官能化聚乙二醇(PEG)缀合的磷脂的聚二甲基硅氧烷(PDMS)壳。数字“基于液滴”的微流控技术能够控制颗粒的组成、大小和多分散性(sigma<10%)。由于热可操纵的固化过程,将 PDMS 用作壳成分可提高混合颗粒的功能和稳定性(寿命>6 个月)。由于具有气核,它们可用作用于创建三维多孔结构和表面的模板材料,不需要繁琐的后处理去除步骤。通过添加具有靶向能力的生物素化 PEG-脂质衍生物,我们通过生物素-亲和素相互作用和芯片上捕获,展示了荧光 IgG 抗体在固定化 PDMS-脂质微泡上的固定化,用于免疫分析。PDMS-脂质组成具有生物相容性和可生物降解性等优点,可用于未来作为多孔工程支架、包装材料或具有细胞靶向能力的递送(例如治疗)剂的体内应用。