Suppr超能文献

基于Box-Behnken质量设计研究的卡培他滨纳米混悬液的处方、优化及设计,以增强抗胃癌疗效

Formulation, Optimization and Design of Capecitabine Nanosuspension to Enhance the Anti-Gastric Cancer Efficacy using Box-Behnken Quality-based Design Study.

作者信息

Khede Mayank Kumar, Nayak Bhabani Shankar, Roy Harekrishna, Nandi Sisir

机构信息

Department of Pharmaceutics, Biju Patnaik University of Technology, Rourkela, 769015, Odisha, India.

Institute of Pharmacy and Technology, Salipur, Cuttack, 754202, Odisha, India.

出版信息

Curr Drug Discov Technol. 2025 Jun 13. doi: 10.2174/0115701638371974250606041312.

Abstract

BACKGROUND

Capecitabine is an anticancer antimetabolite of fluorouracil that inhibits cell proliferation and impairs DNA repair in cancer cells. It is given specifically to treat metastatic breast, gastric and colorectal cancers.

OBJECTIVE

To design, formulate, optimize and evaluate Capecitabine Nanosuspension using the QbD Box-Behnken model.

METHODS

Deploying the Box-Behnken Design (BBD) model, Capecitabine nanosuspension was for-mulated with seventeen runs; the independent variables selected are Pullulan concentration, Poloxamer F407 concentration, and sonication time. The developed nanosuspension was evaluated for particle size, Zeta potential, entrapment efficiency, in vitro drug release, and anti-cancer effectiveness. Drug-excipient compatibility was assessed using the Fourier transform infrared spectroscopy method. X-ray Diffraction studies and Differential Scanning Calorimetry were used to perform and assess the crys-talline nature. Additionally, characteristics of the developed nanosuspension were assessed by per-forming a scanning electron microscopy study.

RESULTS

The effect of various factors on key responses, namely particle size, entrapment efficiency, and drug release up to 8 hours, was assessed. A polynomial equation was employed through the anal-ysis to optimize the formulation, considering the significance levels indicated by the p-values. Notably, these variables demonstrated a substantial influence on the responses. The comparison between ob-served and predicted values revealed a relatively minor variance (85.90, 69.57, and 76.34 for particle size, entrapment efficiency, and percentage drug release at 8 hours, respectively), indicating the mod-el's suitability. The prepared nanosuspension exhibited compatibility with the used excipients, with capecitabine-entrapped nanoparticles uniformly dispersed within the suspending medium.

CONCLUSION

Developed capecitabine nanosuspension demonstrated better efficacy and effectiveness against gastric cancer, with independent variables like pullulan and Poloxamer F207 concentration, along with sonication time, influencing particle size, entrapment efficiency, and drug release.

摘要

背景

卡培他滨是氟尿嘧啶的一种抗癌抗代谢物,可抑制癌细胞的增殖并损害其DNA修复能力。它专门用于治疗转移性乳腺癌、胃癌和结直肠癌。

目的

使用质量源于设计(QbD)的Box-Behnken模型设计、制备、优化并评估卡培他滨纳米混悬液。

方法

采用Box-Behnken设计(BBD)模型,进行17次实验来制备卡培他滨纳米混悬液;选取的自变量为支链淀粉浓度、泊洛沙姆F407浓度和超声处理时间。对所制备的纳米混悬液进行粒径、Zeta电位、包封率、体外药物释放及抗癌效果评估。采用傅里叶变换红外光谱法评估药物-辅料相容性。通过X射线衍射研究和差示扫描量热法进行并评估结晶性质。此外,通过扫描电子显微镜研究评估所制备纳米混悬液的特性。

结果

评估了各种因素对关键响应指标(即粒径、包封率和8小时内的药物释放)的影响。通过分析采用多项式方程来优化制剂,同时考虑p值所表明的显著性水平。值得注意的是,这些变量对响应指标有显著影响。观察值与预测值之间的比较显示差异相对较小(粒径、包封率和8小时药物释放百分比分别为85.90、69.57和76.34),表明该模型适用。所制备的纳米混悬液与所用辅料具有相容性,包载卡培他滨的纳米粒子均匀分散在混悬介质中。

结论

所制备的卡培他滨纳米混悬液对胃癌显示出更好的疗效,支链淀粉和泊洛沙姆F207浓度以及超声处理时间等自变量会影响粒径、包封率和药物释放。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验