4.5 Article

Development of polymeric microparticles for controlled release of bioactive drugs using modified solution enhanced dispersion by supercritical CO2

期刊

JOURNAL OF SUPERCRITICAL FLUIDS
卷 189, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.supflu.2022.105723

关键词

Supercritical CO2; Bioactive drug; Controlled release; Poly (L-lactic acid)

资金

  1. National Natural Science Founda- tion of China [81401535]
  2. CQMU Program for Youth Innovation in Future Medicine [W0055]
  3. Discipline Talents Development Projects of School of Pharmacy [YXY2019XSGG10]
  4. Innovation and Business Pro- jects of Chongqing City [SRIEP202194]
  5. Scientific Research Inno- vation Project of Chongqing Postgraduate [CYS22370]

向作者/读者索取更多资源

Poly(L-lactic acid) microparticles loaded with growth factors were prepared using modified SEDS method, which effectively controlled the release rate while maintaining bioactivity. This study demonstrated the potential of using these carriers for controlled release of bioactive drugs.
Poly (L-lactic acid) microparticles (PLLAms) loaded with growth factors were prepared through the modified (ethanol as the modifier) solution enhanced dispersion by supercritical CO2 (SEDS) for controlling release rate while maintaining bioactivity. Trypsin was used to explore operational parameters and their influence on release. Results showed that the optimized flow rate of polymer solution was 1.0 mL/min. Release rate of trypsin-PLLAms was regulated by molecular weight of PLLA and Polyethylene glycol (PEG) ratio. Bone morphogenetic protein (BMP-2), fibroblast growth factor-2 (FGF-2), and vascular endothelial growth factor (VEGF) was loaded into PLLAms. Encapsulation efficiency was 65.9%, 63.9%, and 64.3%, cumulative release rate was 63.2%, 74.8% and 84.1% for 7 days, respectively. BMP-2, VEGF and FGF-2 released from PLLAms significantly promoted cell proliferation and differentiation. Therefore, the modified SEDS effectively maintained drug bioactivity, which could be used to fabricate carriers for controlled bioactive drugs release.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据