复方多泡脂质体的计算设计与优化

IF 3.4 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Mengjie Rui, Yali Su, Haidan Tang, Yinfeng Li, Naying Fang, Yingying Ge, Qiuqi Feng, Chunlai Feng
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引用次数: 0

摘要

研究了迷迭香酸(RA)、绿原酸(CA)、天scoparone (SCO)等中药复方制剂在多泡脂质体(MVLs)中的协同抗肿瘤作用。优化配方和工艺参数是实现这三种具有不同性质的化合物的有效脂质体包封和最佳释放特性的必要条件。传统的试错法对于复杂的多复合MVLs的优化是低效的。我们建立了一个新的配方优化模型,可以通过预测复合MVLs的最佳配方来解决这一问题。我们的机器学习模型集成了支持向量机回归(SVR)算法和布谷鸟搜索(CS)算法,得到了三个CS-SVR模型来预测单个复合mvl。采用不同权重规则的CS算法,在三种CS- svr模型中搜索最佳配方参数,以最大限度地提高三种化合物的包封效率。随后在预测条件下制备了多化合物mlv,最佳粒径为15.12µm, CA的包封效率为82.93±2.43%,RA的包封效率为82.22±1.25%,SCO的包封效率为95.60±0.18%。通过体外表征和体内抗肿瘤实验进一步验证了预测的最佳复合MVLs,显示出与体外结果一致的良好协同抗肿瘤作用。该模型准确预测了最佳封装条件,并通过实验验证,证明了封装效率的提高和试错次数的减少。总的来说,我们的模型为多化合物MVLs配方提供了预测途径,表明该模型能够显著减轻实验负担,加快配方开发。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Computational Design and Optimization of Multi-Compound Multivesicular Liposomes for Co-Delivery of Traditional Chinese Medicine Compounds

Study explored the synergistic anti-tumor effects of a combination of compounds from Traditional Chinese Medicine, including rosmarinic acid (RA), chlorogenic acid (CA), and scoparone (SCO), in the formulation of multivesicular liposomes (MVLs). Optimization of formulations and process parameters was essential to achieve effective liposomal encapsulation and optimal release profiles for these three compounds with diverse properties. Traditional trial-and-error approaches are inefficient for the optimization of complex multi-compound MVLs. We developed a new formulation optimization model, which could address this issue by predicting the optimal multi-compound MVLs formulation. Our machine learning model integrated support vector machine regression (SVR) algorithm and cuckoo search (CS) algorithm, resulting in three CS-SVR models to predict single-compound MVLs. The CS algorithm, with various weighting rules, was then applied to search the best formulation parameters across three CS-SVR models and to maximize the encapsulation efficiency for all three compounds. The multi-compound MLVs were subsequently prepared under the predicted conditions, achieving an optimized particle size of 15.12 µm, with encapsulation efficiencies of 82.93 ± 2.43% for CA, 82.22 ± 1.25% for RA, and 95.60 ± 0.18% for SCO. The predicted optimal multi-compound MVLs were further validated through in vitro characterization and in vivo anti-tumor experiments, showing a promising synergistic anti-tumor effect consistent with in vitro results. This model accurately predicted optimal encapsulation conditions, which were validated experimentally, demonstrating improved encapsulation efficiencies and reduced trial-and-error iterations. Collectively, our model provides a predictive pathway for multi-compound MVLs formulation, indicating the ability of this model to significantly reduce experimental burden and accelerate formulation development.

Graphical Abstract

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来源期刊
AAPS PharmSciTech
AAPS PharmSciTech 医学-药学
CiteScore
6.80
自引率
3.00%
发文量
264
审稿时长
2.4 months
期刊介绍: AAPS PharmSciTech is a peer-reviewed, online-only journal committed to serving those pharmaceutical scientists and engineers interested in the research, development, and evaluation of pharmaceutical dosage forms and delivery systems, including drugs derived from biotechnology and the manufacturing science pertaining to the commercialization of such dosage forms. Because of its electronic nature, AAPS PharmSciTech aspires to utilize evolving electronic technology to enable faster and diverse mechanisms of information delivery to its readership. Submission of uninvited expert reviews and research articles are welcomed.
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