Box-Behnken设计-响应面法结合BP神经网络法优化经典名方泻白颗粒成型工艺

Optimization of the Molding Process of Classical Prescription Xiebai Granules Based on Box-Behnken Design-Response Surface Method and BP Neural Network Method

  • 摘要:
    目的 Box-Behnken设计-响应面法结合BP神经网络法优化泻白颗粒成型工艺,并建立物理指纹图谱,评价不同批次间颗粒质量的一致性。
    方法 以干膏粉为主药,采用干法制粒,以颗粒的成型率、溶化率、吸湿率、休止角为评价指标,先用单因素试验结合单纯形设计法和熵权法对泻白颗粒的辅料糊精、麦芽糊精、乳糖进行辅料配比筛选,优选出最佳辅料配比;采用熵权法结合Box-Behnken设计-响应面法和BP神经网络算法优选工艺参数,并进行工艺验证;采用物理指纹图谱对泻白颗粒的二级物理属性指标松密度(Da)、吸湿性(H)、水分(HR)、振实密度(Dc)、休止角(α)、豪斯纳比(IH)、相对均齐度指数(Iθ)、卡尔指数(IC)、颗粒间孔隙数(Ie)进行综合表征,评价不同批次颗粒质量的一致性。
    结果 最佳辅料配比为糊精15%,麦芽糊精48%,乳糖37%。最佳工艺参数为输料转速95 r·min-1,压轮转速4 r·min-1,液压压力7 MPa。5批次泻白颗粒的物理指纹图谱相似度均>0.98。
    结论 经优化得到的泻白颗粒成型工艺稳定可行,不同批次泻白颗粒质量稳定,可为泻白颗粒的开发及工业化放大生产提供参考。

     

    Abstract:
    OBJECTIVE To optimize the molding process of Xiebai Granules (XG) using the Box-Behnken design-response surface method combined with the BP neural network method, and to evaluate the consistency of particle quality between different batches by establishing physical fingerprint.
    METHODS Dry paste powder was used as the main drug, dry granulation was adopted, and the forming rate, dissolution rate, moisture absorption rate and angle of repose of the granules were used as evaluation indexes, the excipients dextrin, maltodextrin and lactose of the particles, were screened by single factor test combined with simplex-lattice design and entropy weight method, and the optimal excipient ratio was selected. The entropy weight method combined with the Box-Behnken design-response surface method and the BP neural network algorithm were used to optimize the process parameters, and the process verification was carried out. The physical fingerprint was used to comprehensively characterize the bulk density (Da), hygroscopicity (H), moisture (HR), tap density (Dc), angle of repose (α), Hausner ratio (IH), relative uniformity index (Iθ), Carr index (IC), and interparticle pore number (Ie), and the consistency of particle quality in different batches was evaluated.
    RESULTS The optimal ratio of excipients was dextrin 15%, maltodextrin 48%, and lactose 37%. The optimal process parameters were conveying speed 95 r ·min-1, pressure wheel speed 4 r ·min-1 and hydraulic pressure 7 MPa. The similarity of the physical fingerprints of the five batches of XG was greater than 0.98.
    CONCLUSION The optimized molding process of XG is stable and feasible, and the quality of different batches of XG is stable, which can provide a reference for the development and industrial scale-up production of XG.

     

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