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Release of a Model Antigen from Pellets prepared by Compression of Quil A-Cholesterol-Phospholipid PowderMixtures forming ISCOMs upon Hydration

机译:从通过水合形成ISCOM的Quil A-胆固醇-磷脂粉末混合物压缩制备的小球中释放模型抗原

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Quil A-cholesterol-phospholipid powder mixturescontaining the model antigen PE-FITC-OVA wereprepared by physical mixing or by freeze-drying ofaqueous dispersions of these components in ratios thatallow the formation of ISCOMs. Lipid powder mixtureswere compressed to form small pellets. Release of PEFITC-OVA from the compressed pellets was investigated.Negative staining transmission electron microscopy (TEM)was used to characterize the type of colloids formed uponhydration of compressed pellets. PE-FITC-OVA wasreleased from the pellets in a sustained manner. Pelletsprepared by compression of freeze-dried powders releasedPE-FITC-OVA slower than those prepared from physicallymixed powders. TEM investigations revealed that theantigen was released in form of ISCOMs especially frompellets prepared by compression of freeze-dried powders.The addition of excess cholesterol to lipid powders sloweddown release of antigen. The results obtained in this studyare important in formulating solid Quil A-lipid mixtures assustained release particulate delivery systems for antigen.
机译:通过物理混合或通过冷冻干燥这些组分的水分散体以允许形成ISCOM的比例制备包含模型抗原PE-FITC-OVA的Quil A-胆固醇-磷脂粉末混合物。脂质粉末混合物被压缩形成小颗粒。研究了PEFITC-OVA从压片中的释放。采用负染色透射电子显微镜(TEM)表征了压片水合后形成的胶体类型。 PE-FITC-OVA持续释放。通过压缩冷冻干燥的粉末制备的颗粒释放的PE-FITC-OVA比从物理混合的粉末制备的释放的速度慢。 TEM研究表明,抗原以ISCOM形式释放,特别是通过压缩冻干粉制成的丸粒释放出来。脂质粉中添加过量胆固醇会减缓抗原释放。在这项研究中获得的结果对于配制固体Quil A-脂质混合物作为抗原的缓释颗粒递送系统非常重要。

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