基于Box-Behnken设计和结肠靶向期望函数的5-氟尿嘧啶微珠优化设计方法

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of Pharmaceutical Innovation Pub Date : 2023-09-04 DOI:10.1007/s12247-023-09772-z
Amit Kumar Pandey, Udaivir Singh Sara
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引用次数: 0

摘要

目的 主要目的是通过方框-贝肯设计(BBD)和可取性函数开发和优化 5-氟尿嘧啶的多颗粒体系,并对优化后的批次进行包衣,以提高治疗结直肠癌的疗效和靶向性。方法 通过优化了解多颗粒体系配方中涉及的因素和质量问题至关重要。采用离子凝胶法创建优化批次,选定海藻酸钠、果胶浓度和固化时间等自变量对 5-氟尿嘧啶载药微粒的粒度和包埋效率等响应变量的影响。利用 Design-Expert 生成的等值线、响应面设计、数学计算和可取函数,研究了自变量和因变量之间的关系。与预期值和理想函数相比,观察到的答案非常相似,偏差小于 5%。第二层 Eudragit S100 涂覆在改进配方上。涂层微珠的 pH 值释放率低于 10%。10 小时后,超过 55.12% 的药物被释放到肠道区域(pH 值为 6.8)。动力学研究表明,根据 Higuchi 和 Korsmeyer-Peppas 模型创建的配方具有线性关系,如图所示,R2 值分别为 0.9887 和 0.9236。结论本研究中制作的微珠可将药物输送到所需的位置。所开发的微珠可能是由小颗粒制成的,其中含有较高比例的药物。研究结果表明,多微粒可能是一种向结肠输送药物的载体,Box-Behnken 设计和可取性功能可以作为优化配方的积极策略。将其配制成多微粒后,其细胞毒性得以保持,也适合结肠直肠癌患者服用。
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Quality by Design Approach for Optimization of 5-Fluorouracil Microbeads Using Box–Behnken Design and Desirability Function for Colon Targeting

Purpose

The main objective was to develop and optimize a multiparticulate system of 5-fluorouracil through the Box–Behnken design (BBD) and desirability function and coating of the optimized batch for increased therapeutic efficacy and targeting for the treatment of colorectal cancer.

Method

It is essential to understand the factors and quality aspects involved in the formulation of a multiparticulate system through optimization. The ionotropic gel method was used to create an optimized batch, with selected independent factors such as sodium alginate, pectin concentrations, and curing time on the response variables such as particle size and entrapment efficiency of 5-fluorouracil-loaded microparticle. The relationship between the independent and dependent variables was examined by utilizing the contour, response surface designs, mathematical calculations, and desirability function produced by Design-Expert.

Result

The ionotropic gelation process was used to create an optimized batch, and the generated microparticles had a 674 µm particle size and a 90.81% drug entrapment efficiency. The observed answers were very similar with a bias of less than 5% when compared to the expected value and desirability function. A second layer of Eudragit S100 was applied to the improved formulation. The coated microbeads released pH 1.2 at a rate of less than 10%. After 10 h, more than 55.12% of the drug was released into the intestinal area (pH 6.8). The kinetics investigation demonstrated that the created formulation for the Higuchi and Korsmeyer-Peppas models possessed linearity, as shown by the plots, with R2 values of 0.9887 and 0.9236, respectively. This outcome supported the formulation’s extended-release behavior.

Conclusion

It was suggested that the drugs would be delivered to the desired place using the microbeads created in this study. The developed microbeads were probably made of small particles that contained a high percent drug entrapment. According to the findings, multiparticulate can be a possible carrier for the delivery of drugs to the colon, and the Box–Behnken design and desirability function can be an active strategy for optimizing the formulation. Its cytotoxicity is maintained by being formulated as a multiparticulate, and it is also suited for administration to patients with colorectal cancer.

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来源期刊
Journal of Pharmaceutical Innovation
Journal of Pharmaceutical Innovation PHARMACOLOGY & PHARMACY-
CiteScore
3.70
自引率
3.80%
发文量
90
审稿时长
>12 weeks
期刊介绍: The Journal of Pharmaceutical Innovation (JPI), is an international, multidisciplinary peer-reviewed scientific journal dedicated to publishing high quality papers emphasizing innovative research and applied technologies within the pharmaceutical and biotechnology industries. JPI''s goal is to be the premier communication vehicle for the critical body of knowledge that is needed for scientific evolution and technical innovation, from R&D to market. Topics will fall under the following categories: Materials science, Product design, Process design, optimization, automation and control, Facilities; Information management, Regulatory policy and strategy, Supply chain developments , Education and professional development, Journal of Pharmaceutical Innovation publishes four issues a year.
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