载阿霉素明胶微球治疗骨肿瘤的研究

Shaolong Zhou, Xiu-Ya Shi, Yi Chen, Li Li, Chen Chen
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引用次数: 1

摘要

目的:研究阿霉素-明胶微球(ADM-GMS)的性质和体外释放特性,探讨其对人骨肉瘤U-20s细胞株的影响及其作用机制。方法:采用乳化交联法制备ADM-GMS。采用扫描电镜观察微球的形状,采用激光粒度仪测量颗粒大小和分布。采用紫外分光光度法计算载药率和包封率,并评价微球对阿霉素(ADM)的释放性能。采用细胞计数试剂盒-8 (CCK-8)法评价ADM-GMS对人骨肉瘤U-20s细胞株的体外抗肿瘤活性。结果:ADM-GMS的最佳配比为1:10,制备的微球呈圆形,分散性好。最佳料比的平均粒径为14.02±1.67μm,载药率为6.05±0.26%,包封率为84.27±3.10%。ADM-GMS具有优异的缓释性能,对人骨肉瘤u -20的生长有明显的抑制作用。结论:材料比为1:1制备的ADM-GMS具有较好的缓释能力和较低半抑制浓度的抗骨肿瘤作用。因此,这种ADM明胶给药系统值得进一步的临床研究。然而,本研究的检测方法简单,临床试验支持薄弱,需要更多的研究来进一步验证。
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Adriamycin-loaded Gelatin Microspheres in the Treatment of Bone Tumors
Objective: This study harnessed adriamycin-loaded gelatin microspheres (ADM-GMS) to examine their properties and in vitro release characteristics, and explore their effect on human osteosarcoma U-20s cell strain and its mechanism. Methods: ADM-GMS was prepared using the emulsification-crosslinking method. The scanning electron microscope was employed to observe the shape of microspheres, and particle size and distribution were measured using a laser particle size device. The drug loading rate and encapsulation rate were calculated by ultraviolet spectrophotometry, and the drug release performance of the microspheres to adriamycin (ADM) was evaluated. The cell counting kit-8 (CCK-8) method was used to evaluate the anti-tumor activity of ADM-GMS on human osteosarcoma U-20s cell strain in vitro. Results: We determined an optimal material ratio of 1:10 for ADM-GMS, with which the microspheres showed a round shape and excellent dispersity. The average particle size with the optimal material ratio was 14.02±1.67μm, with a drug loading rate of 6.05±0.26% and an encapsulation rate of 84.27±3.10%. ADM-GMS had excellent sustained-release properties and a significant inhibitory effect on the growth of human osteosarcoma U-20s. Conclusion: ADM-GMS, prepared with a material ratio of 1:1, has a promising slow-release ability and an anti-bone tumor effect with a lower Semi-inhibitory concentration. Thus, this ADM gelatin delivery system is worthy of further clinical research. However, the detection method in this study is simple and weakly supported by clinical trials, and more investigations are required for further verification.
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