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Study on the preparation of hydroxycamptothecin semisolid lipid nanoparticles by orthogonal design

机译:正交设计研究羟基胺素羟基固体脂质纳米粒子的研究

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Objective: To prepare hydroxycamptothecin semisolid lipid nanoparticles (HCPT-SSLN). Methods: Based on the single-factor experiment, the HCPT-SSLN was prepared by using orthogonal design for optimization of formulation and technology. Then the obtained SSLN was also evaluated. Results: The mean particle size of the prepared HCPT-SSLN was 130.5nm, Polydispersity Index (PI) was 0.18, drag loading (DL) was 2.51%, entrapment efficiency (EE) was 79.19%, ζ potential was -33.1mV; Placed at 4°C for 6 months, the appearance, particle size and entrapment efficiency of SSLN were all stable. Conclusion: The HCPT-SSLN has high entrapment efficiency and drug loading, uniform particle size, good stability, which provides an extensive prospect for clinical application of HCPT.
机译:目的:制备羟基清除素半固体脂质纳米颗粒(HCPT-SSLN)。方法:基于单因素实验,通过使用正交设计来制备HCPT-SSLN以优化配方和技术。然后还评估所获得的SSLN。结果:制备的HCPT-SSLn的平均粒度为130.5nm,多分散指数(PI)为0.18,拖曳载荷(DL)为2.51%,夹紧效率(EE)为79.19%,潜力为-33.1mV;置于4°C 6个月,SSLN的外观,粒度和咬夹效率都稳定。结论:HCPT-SSLN具有高的夹带效率和药物负荷,均匀的粒度,稳定性良好,为HCPT的临床应用提供了广泛的前景。

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