首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >Paclitaxel distribution in poly(ethylene glycol)/poly(lactide-co-glycolic acid) blends and its release visualized by coherent anti-Stokes Raman scattering microscopy
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Paclitaxel distribution in poly(ethylene glycol)/poly(lactide-co-glycolic acid) blends and its release visualized by coherent anti-Stokes Raman scattering microscopy

机译:紫杉醇在聚乙二醇/聚丙交酯-乙醇酸共混物中的分布及其释放,通过相干抗斯托克斯拉曼散射显微镜观察

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摘要

Mechanisms underlying the release of paclitaxel (PTX) from poly(ethylene glycol)/poly(lactic-co-glycolic acid) (PEG/PLGA) blends were investigated by coherent anti-Stokes Raman scattering (CARS) microscopy. PLGA, PEG, and PTX were selectively imaged by using the resonant CARS signal from the CH3, CH2, and aromatic CH stretch vibrations, respectively. Phase segregation was observed in PLGA films containing 10 to 40 wt.% PEG in the absence of PTX loading. The PEG phase existed in the form of crystalline fibers in the (8:2, weight ratio) and (7:3) PLGA/ PEG films. CARS observation indicated that PTX preferentially partitioned into the PEG domains in the (9:1) and (8:2) PLGA/PTX films, but exhibited a uniform mixing with both PLGA and PEG in the (7:3) PLGA/PEG film. The solid dispersion of PTX into PEG domains was attributed to a strong interaction between PTX and PEG, supported by the disappearance of PEG crystallization in the PTX-loaded PLGA/PEG film evidenced through X-ray diffraction analysis. PTX release was induced by exposing the film to an aqueous solution and monitored in real time by CARS and two-photon fluorescence microscopy. Fast dissolution of both PEG and PTX was observed at the film surface. Upon infiltration of water into the film, the PEG domains were rearranged into ring structures enriched by both PTX and PEG. The CARS data provided visual evidence explaining the accelerated burst release followed by more sustained release of PTX from the PLGA/PEG films as measured by HPLC. (c) 2007 Elsevier B.V. All rights reserved.
机译:通过相干抗斯托克斯拉曼散射(CARS)显微镜研究了紫杉醇(PTX)从聚(乙二醇)/聚(乳酸-乙醇酸共聚物)(PEG / PLGA)混合物中释放的潜在机理。使用来自CH3,CH2和芳香族CH拉伸振动的共振CARS信号分别对PLGA,PEG和PTX进行选择性成像。在不存在PTX负载的情况下,在含有10至40重量%PEG的PLGA膜中观察到相分离。 PEG相以结晶纤维的形式存在于(8:2,重量比)和(7:3)PLGA / PEG膜中。 CARS观察表明PTX在(9:1)和(8:2)PLGA / PTX膜中优先分配到PEG域中,但在(7:3)PLGA / PEG膜中与PLGA和PEG均匀混合。 PTX在PEG域中的固体分散体归因于PTX和PEG之间的强相互作用,这通过X射线衍射分析证明,在载有PTX的PLGA / PEG膜中PEG结晶消失。通过将膜暴露于水溶液中诱导PTX释放,并通过CARS和双光子荧光显微镜实时监控。在膜表面观察到PEG和PTX都快速溶解。当水渗入膜中时,PEG结构域被重排成富含PTX和PEG的环结构。 CARS数据提供了直观的证据,解释了如通过HPLC测定的,PTX从PLGA / PEG膜中加速释放并随后持续释放。 (c)2007 Elsevier B.V.保留所有权利。

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