湿介质研磨法制备槲皮素纳米混悬剂的工艺及配方参数研究。

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Pegah Cheshmehnoor, Noushin Bolourchian, Erfan Abdollahizad, Arash Derakhshi, Simin Dadashzadeh, Azadeh Haeri
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引用次数: 0

摘要

背景:大量新物质由于溶出速度慢、溶解度差,口服给药的生物制药性能不足。目的:采用纳米研磨的方法改善疏水药物槲皮素的理化性质。方法:采用湿磨法制备槲皮素纳米混悬液,冷冻干燥。确定稳定剂的种类和配比、药物含量、磨粒时间和颗粒大小为关键变量,并评估其对槲皮素粒径的影响。通过形貌、结晶度、分子相互作用、饱和溶解度和溶解性能对优化后的纳米晶体进行了表征。结果:在优化的工艺条件下,转速为500转/分,0.3 ~ 0.4 mm氧化锆珠磨18次,最小粒径为281.21 nm, PDI值为0.22。纳米晶体呈棒状纳米结构,XRD扫描证实药物结晶度下降。优化后的配方具有较高的溶解度和溶出率,良好的物理稳定性。结论:介质磨粒技术是提高疏水药物溶解度的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Particle Size Tailoring of Quercetin Nanosuspensions by Wet Media Milling Technique: A Study on Processing and Formulation Parameters.

Particle Size Tailoring of Quercetin Nanosuspensions by Wet Media Milling Technique: A Study on Processing and Formulation Parameters.

Particle Size Tailoring of Quercetin Nanosuspensions by Wet Media Milling Technique: A Study on Processing and Formulation Parameters.

Particle Size Tailoring of Quercetin Nanosuspensions by Wet Media Milling Technique: A Study on Processing and Formulation Parameters.

Background: A large number of new substances have insufficient biopharmaceutical properties for oral administration caused by their slow dissolution rate and poor solubility.

Objective: The purpose of our experiment was to improve the physicochemical properties of a hydrophobic drug, quercetin, by the nanomilling approach.

Methods: Quercetin nanosuspensions were prepared using a wet-milling method followed by lyophilization. Stabilizer type and ratio, drug content, milling time, and bead size were identified as critical variables, and their impacts on quercetin particle size were assessed. The optimized nanocrystal was characterized by its morphology, crystallinity, molecular interactions, saturation solubility, and dissolution properties.

Results: At optimized process conditions of milling at 500 rpm for 18 cycles of grinding with 0.3 - 0.4 mm zirconium oxide beads, minimum particle size, and PDI values were 281.21 nm and 0.22, respectively. Nanocrystals showed rod-like nanostructures, and XRD scans confirmed a decrease in drug crystallinity. The optimized formulation showed increased solubility and dissolution rate, as well as good physical stability.

Conclusions: Particle size reduction by media milling technique was an efficient method for the solubility enhancement of hydrophobic drugs.

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来源期刊
CiteScore
3.40
自引率
6.20%
发文量
52
审稿时长
2 months
期刊介绍: The Iranian Journal of Pharmaceutical Research (IJPR) is a peer-reviewed multi-disciplinary pharmaceutical publication, scheduled to appear quarterly and serve as a means for scientific information exchange in the international pharmaceutical forum. Specific scientific topics of interest to the journal include, but are not limited to: pharmaceutics, industrial pharmacy, pharmacognosy, toxicology, medicinal chemistry, novel analytical methods for drug characterization, computational and modeling approaches to drug design, bio-medical experience, clinical investigation, rational drug prescribing, pharmacoeconomics, biotechnology, nanotechnology, biopharmaceutics and physical pharmacy.
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