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采用新型固-油-油-水乳液法制备的粒细胞集落刺激因子长效微球。

Sustained-release G-CSF microspheres using a novel solid-in-oil-in-oil-in-water emulsion method.

机构信息

Department of Vascular Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Int J Nanomedicine. 2012;7:4559-69. doi: 10.2147/IJN.S33993. Epub 2012 Aug 17.

Abstract

BACKGROUND

The main treatments for cancers are still chemotherapy and radiotherapy for intermediate-stage cancer and terminal cancer. However, the therapeutic methods often result in a decreased neutrophilic granulocyte count and other side effects. In this study, in order to improve the neutrophilic granulocyte levels in the blood after radiotherapy and chemotherapy, we developed a sustained-release granulocyte colony-stimulating factor (G-CSF) microsphere formulation using a novel solid-in-oil-in-oil-in-water (S/O/O/W) emulsification method.

METHODS

G-CSF was loaded into dextran nanoparticles by freezing-induced phase separation, and then the G-CSF-loaded nanoparticles were encapsulated into sustained-release poly(lactic-co- glycolic acid) microspheres using S/O/O/W emulsification. The control microspheres were also prepared through W/O/W emulsification. The performance of the two microsphere formulations was investigated both in vitro and in vivo.

RESULTS

The microspheres for the controlled release of G-CSF in a zero-order or near-zero-order pattern were provided for 2 weeks. The in vitro cumulative G-CSF release kept over 90% of its bioactivity, which was proved by a NFS-60 cell line growth assay. The microspheres of the control group fabricated by W/O/W emulsification maintained less then half of its bioactivity. The in vivo efficacy of microspheres made using the S/O/O/W method was higher than those using the W/O/W method.

CONCLUSION

These results suggested that the microspheres prepared by the S/O/O/W method had increased neutrophil activity compared to those prepared by W/O/W.

摘要

背景

癌症的主要治疗方法仍然是化疗和放疗,适用于中期癌症和晚期癌症。然而,这些治疗方法往往会导致中性粒细胞计数下降等副作用。在本研究中,为了提高放化疗后血液中的中性粒细胞水平,我们采用一种新型的固-油-油-水(S/O/O/W)乳化法,开发了一种粒细胞集落刺激因子(G-CSF)的缓释微球制剂。

方法

将 G-CSF 载入葡聚糖纳米粒中,通过冷冻诱导相分离,然后将载有 G-CSF 的纳米粒用 S/O/O/W 乳化法包封入缓释聚乳酸-聚乙二醇酸(PLGA)微球中。同时也制备了 W/O/W 乳化法的对照微球。考察了两种微球制剂的体内外性能。

结果

提供了一种 G-CSF 零级或近零级释放的微球,持续释放时间为 2 周。体外累积 G-CSF 释放保持超过 90%的生物活性,这通过 NFS-60 细胞系生长试验得到了证明。W/O/W 乳化法制备的对照组微球的生物活性保持在其一半以下。S/O/O/W 法制备的微球的体内疗效高于 W/O/W 法制备的微球。

结论

这些结果表明,与 W/O/W 法相比,S/O/O/W 法制备的微球具有更高的中性粒细胞活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bea/3423650/ab08b929bad5/ijn-7-4559f1.jpg

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