Development, Characterization, and Molecular Dynamics Simulation of Andrographolide Nanosuspensions Utilizing Hummer Acoustic Resonance Technology.

IF 3.4 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Li Wang, Xiaoyang Zhang, Jianlu Qu, Zhanrui Zhang, Wei Wu, Wenlong Li
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Abstract

Andrographolide (AG) is a diterpenoid lactone, widely recognized for its potent anti-inflammatory and immunomodulatory properties. However, AG's clinical applications are significantly limited due to its poor water solubility. The aim of this study was to rapidly develop an andrographolide nanosuspension (AG-NS) using Hummer Acoustic Resonance (HAR) technology to enhance AG's solubility. AG-NS was prepared using HAR technology for high-throughput screening of stabilizers. Quality risk assessment was performed to identify critical formulation and process variables influencing AG-NS. A Box-Behnken design (BBD) was applied to evaluate the effects of these critical variables on AG-NS. Following lyophilization, the redispersibility of AG-NS was evaluated, and physicochemical characterization was conducted to verify the absence of significant interactions between AG and the excipients. The optimized AG-NS formulation exhibited a Z-Ave of 183.96 ± 4.40 nm, a PDI of 0.151 ± 0.065, and a zeta potential of -42.85 ± 1.09 mV. MD simulations revealed the internal mechanisms of AG-NS stabilization. Lyophilized AG-NS demonstrated excellent redisperseability. In vitro dissolution studies showed that the lyophilized AG-NS had a significantly faster dissolution rate and higher cumulative dissolution (120 min) compared to AG crude powder and the physical mixture (PM). The optimized AG-NS demonstrated favorable physicochemical properties and enhanced dissolution performance. The lyophilized formulation exhibited excellent redispersibility upon reconstitution. HAR technology is an innovative and efficient approach for the rapid development and optimization of nanosuspension formulations.

利用Hummer声学共振技术开发、表征和分子动力学模拟穿心莲内酯纳米悬浮液。
穿心莲内酯(AG)是一种二萜内酯,因其有效的抗炎和免疫调节特性而被广泛认可。然而,AG的水溶性较差,极大地限制了其临床应用。本研究的目的是利用Hummer Acoustic Resonance (HAR)技术快速制备穿心莲内酯纳米混悬液(AG- ns),以提高AG的溶解度。采用HAR技术制备AG-NS,对稳定剂进行高通量筛选。进行质量风险评估以确定影响AG-NS的关键配方和工艺变量。采用Box-Behnken设计(BBD)评价这些关键变量对AG-NS的影响。冻干后,对AG- ns的再分散性进行了评估,并进行了物理化学表征以验证AG与辅料之间没有明显的相互作用。优化后的AG-NS配方的Z-Ave为183.96±4.40 nm, PDI为0.151±0.065,zeta电位为-42.85±1.09 mV。MD模拟揭示了AG-NS稳定化的内部机制。冻干AG-NS表现出优异的再分散性。体外溶出试验表明,冻干AG- ns的溶出速率和累积溶出量(120 min)均显著高于AG粗粉和物理混合物(PM)。优化后的AG-NS具有良好的理化性能和增强的溶出性能。冻干制剂在重构后表现出优异的再分散性。HAR技术是快速开发和优化纳米悬浮液配方的一种创新和有效的方法。
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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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