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Study of erythrocytes as a novel drug carrier for the delivery of artemether

机译:作为一种用于递送刷籽的新药载体的红细胞研究

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Resealed erythrocytes have been explored in various dimensions of drug delivery, owing to their high biocompatibility and inability to initiate immune response. The present research was designed to evaluate the drug delivery potential of erythrocytes by loading a hydrophobic anti-malarial drug, Artemether. Three different loading techniques were applied to achieve maximum optimized drug loading. A HPLC method was validated for drug quantification in erythrocytes. The relatively high loading was achieved using hypotonic treatment was 31.39% as compared to other two methods. These, drug loaded erythrocytes were characterized for membrane integrity via ESR showing higher ESR values for drug loaded cells as compared to normal cells. Moreover, microscopic evaluation was done to observe morphological changes in erythrocytes after successful loading which showed swollen cells with slight rough surface as compared to smooth surface of normal cells. Drug release was studied for 8 h which showed more than 80% release within 3-7 h from erythrocytes treated with different hypotonic methods. Overall, the study revealed a potential application of erythrocytes in delivery of hydrophobic drugs using hypotonic treatment as compared to other methods.
机译:由于其高生物相容性和无法引发免疫应答,已经在药物递送的各种尺寸中探讨了重新密封的红细胞。本研究旨在通过装载疏水性抗疟疾药物,蒿甲醚来评估红细胞的药物输送潜力。采用三种不同的装载技术来实现最大优化的药物载荷。验证了HPLC方法以用于红细胞中的药物量化。与其他两种方法相比,使用低辐射处理实现的相对高的负载量为31.39%。这些,药物负载的红细胞通过ESR表征膜完整性,显示与正常细胞相比的药物负载细胞的较高ESR值。此外,与正常细胞的光滑表面相比,在成功负载后,进行了微观评估以观察成功负载后的红细胞的形态变化。研究了药物释放8小时,其在用不同的低渗方法处理的红细胞中显示出超过80%的释放。总体而言,该研究揭示了与其他方法相比,使用低渗处理潜在应用红细胞在疏水药物中递送疏水药物。

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