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首页> 外文期刊>Nanomedicine research journal. >Caffeic Acid Phenethyl Ester Loaded Poly (ε -caprolactone) Nanoparticles for Improved Anticancer Efficacy: Formulation Development, Characterization and in Vitro Cytotoxicity Study
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Caffeic Acid Phenethyl Ester Loaded Poly (ε -caprolactone) Nanoparticles for Improved Anticancer Efficacy: Formulation Development, Characterization and in Vitro Cytotoxicity Study

机译:用于改善抗癌疗效的咖啡酸苯乙烷纳米粒子纳米粒子:配方发育,表征和体外细胞毒性研究

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Caffeic acid phenethyl ester (CAPE) is a active constituent of propolis and well known for its anticancer potential. The therapeutic efficacy of CAPE is limited with its poor water solubility and low bioavailability. In present study CAPE loaded Poly (ε-caprolactone) nanoparticles formulation (denoted as CPL) was designed and investigated to improve solubility, achieve sustained drug release and enhance anticancer efficacy. Formulation development, characterization and optimization were carried out by design of experiment approach. Developed formulations were evaluated in detail for nanoparticle characterization and in vitro cytotoxicity study. Developed nanoparticles showed particle size and encapsulation efficiency of 187 ± 2 - 220 ± 2 nm and 64.37+ 1.20- 74.80+ 1.45% respectively. Optimized formulation showed sustained drug release over a period of 36 h. Moreover, concentration of the drug needed for total growth inhibition of cells in a designed time period (TGI) was decreased by 40.87% for CPL as compared to CAPE in human breast cancer MCF-7 cells and 23.73% in human colon cancer cells HT-29 indicating improved cytotoxicity of CAPE. The study proven that the developed CPL exhibited improved solubility, sustained drug release, enhanced in vitro cytotoxicity in MCF-7 and HT-29 cell lines in comparison with pure CAPE. Thus the proposed system may be served as a useful tool for cancer treatment.
机译:咖啡酸苯乙烷酯(Cape)是蜂股母的活性组分,均以抗癌潜力均为众所周知的。辣椒的治疗效果受到其水溶解度差和低生物利用度的限制。在本研究中,设计并研究了装载的聚(ε-己内酯)纳米颗粒制剂(表示为CPL),以改善溶解度,实现持续的药物释放并增强抗癌功​​效。通过实验方法设计进行制剂,表征和优化。详细评估了开发的制剂,用于纳米粒子表征和体外细胞毒性研究。开发的纳米颗粒显示粒度和封装效率为187±2-220±2nm和64.37+ 1.20-74.80 + 1.45%。优化的制剂显示出持续的药物释放在36小时内。此外,与人乳腺癌MCF-7细胞中的CPE相比,CPL在人乳腺癌MCF-7细胞中的浓度降低了40.87%,在人结肠癌细胞中减少了40.87%所需的药物抑制的浓度。 29表明披着披肩的改善细胞毒性。该研究证明,发达的CPL表现出改善的溶解度,持续的药物释放,与纯斗孔相比,MCF-7和HT-29细胞系中的体外细胞毒性增强。因此,所提出的系统可以用作癌症治疗的有用工具。

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