首页> 外文期刊>Biomaterials >BIODEGRADABLE POLYMERIC MICROPARTICLES FOR DRUG DELIVERY AND VACCINE FORMULATION - THE SURFACE ATTACHMENT OF HYDROPHILIC SPECIES USING THE CONCEPT OF POLY(ETHYLENE GLYCOL) ANCHORING SEGMENTS
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BIODEGRADABLE POLYMERIC MICROPARTICLES FOR DRUG DELIVERY AND VACCINE FORMULATION - THE SURFACE ATTACHMENT OF HYDROPHILIC SPECIES USING THE CONCEPT OF POLY(ETHYLENE GLYCOL) ANCHORING SEGMENTS

机译:用于药物输送和疫苗配制的可生物降解的聚合物微粒-使用聚乙烯醇锚固段的概念对亲水性物种进行表面附着

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Poly(ethylene glycol)-dextran (PEG-DEX) conjugates have been used as a combined stabilizer and surface modifier to produce resorbable poly(DL-lactide-co-glycolide) (PLG) microparticles by an emulsification/solvent evaporation technique. The use of PEG or dextran polymers alone was incapable of producing microparticles. Particle size measurements revealed smaller mean particle sizes (480 nm) and improved polydispersity when using a 1.2% PEG substituted conjugate relative to a 9% substituted material (680 nm). PLG microparticles modified by post-adsorbed PEG-DEX conjugates flocculated in 0.01 M salt solutions, whereas PLG microparticles prepared using PEG-DEX as a surfactant were stable in at least 0.5 M NaCl solutions. Surface modification of PLG microparticles was confirmed by zeta potential measurements and surface analysis using X-ray photoelectron spectroscopy. The presence of surface exposed dextran was confirmed by an immunological detection method using a dextran-specific antiserum in an enzyme-linked immunosorbent assay. The findings support a model in which the PEG component of the PEG-DEX conjugate provides an anchor to the microparticle surface while the dextran component extends from the particle surface to contribute a steric stabilization function. This approach offers opportunities for attaching hydrophilic species such as targeting moieties to biodegradable microparticles to improve the interaction of drug carriers and vaccines with specific tissue sites. (C) 1997 Elsevier Science Limited. All rights reserved. [References: 42]
机译:聚(乙二醇)-右旋糖酐(PEG-DEX)共轭物已被用作稳定剂和表面改性剂的组合,通过乳化/溶剂蒸发技术生产可吸收的聚(DL-丙交酯-乙交酯)(PLG)微粒。单独使用PEG或右旋糖酐聚合物不能产生微粒。粒径测量显示,相对于9%取代的材料(680 nm),使用1.2%PEG取代的共轭物时,平均粒径较小(480 nm),多分散性得到改善。经过后吸附的PEG-DEX共轭物改性的PLG微粒在0.01 M盐溶液中絮凝,而使用PEG-DEX作为表面活性剂制备的PLG微粒在至少0.5 M NaCl溶液中稳定。 PLG微粒的表面改性通过zeta电位测量和使用X射线光电子能谱的表面分析得到证实。通过在酶联免疫吸附测定中使用葡聚糖特异性抗血清的免疫学检测方法,确认表面暴露的葡聚糖的存在。这些发现支持了一种模型,其中PEG-DEX缀合物的PEG组分为微粒表面提供了锚点,而右旋糖酐组分则从微粒表面延伸,从而发挥了空间稳定作用。这种方法提供了将诸如靶向部分之类的亲水物质附着到可生物降解的微粒上的机会,以改善药物载体和疫苗与特定组织部位的相互作用。 (C)1997 Elsevier Science Limited。版权所有。 [参考:42]

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