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首页> 外文期刊>Applied Surface Science >Quantitative Tof-sims Studies Of Protein Drug Release From Biodegradable Polymer Drug Delivery Membranes
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Quantitative Tof-sims Studies Of Protein Drug Release From Biodegradable Polymer Drug Delivery Membranes

机译:从可生物降解的聚合物药物递送膜中释放蛋白质药物的定量Tof-sims研究

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Biodegradable polymers are of interest in developing strategies to control protein drug delivery. The protein that was used in this study is Keratinocyte Growth Factor (KGF) which is a protein involved in the re-epithelialization process. The protein is stabilized in the biodegradable polymer matrix during formulation and over the course of polymer degradation with the use of an ionic surfactant Aerosol-OT (AOT) which will encapsulate the protein in an aqueous environment. The release kinetics of the protein from the surface of these materials requires precise timing which is a crucial factor in the efficacy of this drug delivery system. Time-of-flight secondary ion mass spectrometry (ToF-SIMS) was used in the same capacity to identify the molecular ion peak of the surfactant and polymer and use this to determine surface concentration. In the polymer matrix, the surfactant molecular ion peak was observed in the positive and negative mode at m/z 467 and 421, respectively. These peaks were determined to be [AOT + Na~+] and [AOT - Na~+]. These methods are used to identify the surfactant and protein from the polymer matrix and are used to measure the rate of surface accumulation. The second step was to compare this accumulation rate with the release rate of the protein into an aqueous solution during the degradation of the biodegradable film. This rate is compared to that from fluorescence spectroscopy measurements using the protein autofluorescence from that released into aqueous solution [C.M. Mahoney, J. Yu, A. Fahey, J.A.J. Gardella, SIMS depth profiling of polymer blends with protein based drugs, Appl. Surf. Sci. 252 (2006), 6609-6614.].
机译:可生物降解的聚合物在开发控制蛋白质药物递送的策略中受到关注。在这项研究中使用的蛋白质是角质形成细胞生长因子(KGF),是一种与上皮再形成过程有关的蛋白质。在配制期间以及在聚合物降解过程中,使用离子表面活性剂Aerosol-OT(AOT)将蛋白质稳定在可生物降解的聚合物基质中,该表面活性剂会将蛋白质封装在水性环境中。蛋白质从这些材料表面释放的动力学需要精确的时间安排,这是该药物递送系统功效的关键因素。飞行时间二次离子质谱(ToF-SIMS)以相同的容量使用,以识别表面活性剂和聚合物的分子离子峰,并以此来确定表面浓度。在聚合物基质中,分别在m / z 467和421处以正模式和负模式观察到表面活性剂分子离子峰。确定这些峰为[AOT + Na〜+]和[AOT-Na〜+]。这些方法用于从聚合物基质中鉴定表面活性剂和蛋白质,并用于测量表面积累的速率。第二步是将这种累积速率与可生物降解膜降解过程中蛋白质向水溶液中的释放速率进行比较。将该速率与使用释放到水溶液中的蛋白质自发荧光的蛋白质自发荧光的荧光光谱测量结果进行比较[C.M. Mahoney,J. Yu,A.Fahey,J.A.J. Gardella,聚合物掺合物与蛋白质类药物的SIMS深度剖析,Appl。冲浪。科学252(2006),6609-6614。]。

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