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冻干法吸附剂预包衣:一种增强桂利嗪从固体自纳米乳化药物递送系统(S-SNEDDS)中释放的新型绿色溶剂技术。

Adsorbent Precoating by Lyophilization: A Novel Green Solvent Technique to Enhance Cinnarizine Release from Solid Self-Nanoemulsifying Drug Delivery Systems (S-SNEDDS).

作者信息

Tashish Ahmad Yousef, Shahba Ahmad Abdul-Wahhab, Alanazi Fars Kaed, Kazi Mohsin

机构信息

Department of Pharmaceutics, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.

Kayyali Research Chair for Pharmaceutical Industries, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.

出版信息

Pharmaceutics. 2022 Dec 30;15(1):134. doi: 10.3390/pharmaceutics15010134.

Abstract

BACKGROUND

Solidification by high surface area adsorbents has been associated with major obstacles in drug release. Accordingly, new approaches are highly demanded to solve these limitations. The current study proposes to improve the drug release of solidified self-nanoemulsifying drug delivery systems (SNEDDS) to present dual enhancement of drug solubilization and formulation stabilization, using cinnarizine (CN) as a model drug.

METHODS

The solidification process involved the precoating of adsorbent by lyophilization of the aqueous dispersion of polymer-adsorbent mixture using water as a green solvent. Then, the precoated adsorbent was mixed with drug-loaded liquid SNEDDS to prepare solid SNEDDS. The solid-state characterization of developed cured S-SNEDDS was done using X-ray powder diffraction (XRD) and differential scanning calorimetry (DSC). In vitro dissolution studies were conducted to investigate CN SNEDDS performance at pH 1.2 and 6.8. The solidified formulations were characterized by Brunauer-Emmett-Teller (BET), powder flow properties, scanning electron microscopy, and droplet size analysis. In addition, the optimized formulations were evaluated through in vitro lipolysis and stability studies.

RESULTS

The cured solid SNEDDS formula by PVP k30 showed acceptable self-emulsification and powder flow properties. XRD and DSC revealed that CN was successfully amorphized into drug-loaded S-SNEDDS. The uncured solid SNEDDS experienced negligible drug release (only 5% drug release after 2 h), while the cured S-SNEDDS showed up to 12-fold enhancement of total drug release (at 2 h) compared to the uncured counterpart. However, the cured S- SNEDDS showed considerable CN degradation and decrease in drug release upon storage in accelerated conditions.

CONCLUSIONS

The implemented solidification approach offers a promising technique to minimize the adverse effect of adsorbent on drug release and accomplish improved drug release from solidified SNEDDS.

摘要

背景

高比表面积吸附剂固化与药物释放中的主要障碍相关。因此,迫切需要新的方法来解决这些局限性。本研究提出以桂利嗪(CN)为模型药物,改善固化自纳米乳化药物递送系统(SNEDDS)的药物释放,以实现药物增溶和制剂稳定性的双重增强。

方法

固化过程包括以水为绿色溶剂,通过冻干聚合物 - 吸附剂混合物的水分散体对吸附剂进行预包衣。然后,将预包衣的吸附剂与载药液体SNEDDS混合以制备固体SNEDDS。使用X射线粉末衍射(XRD)和差示扫描量热法(DSC)对所开发的固化S - SNEDDS进行固态表征。进行体外溶出研究以考察CN SNEDDS在pH 1.2和6.8条件下的性能。通过布鲁诺尔 - 埃米特 - 泰勒(BET)、粉末流动性、扫描电子显微镜和液滴尺寸分析对固化制剂进行表征。此外,通过体外脂解和稳定性研究对优化后的制剂进行评估。

结果

PVP k30固化的固体SNEDDS配方显示出可接受的自乳化和粉末流动性能。XRD和DSC表明CN成功地非晶化进入载药S - SNEDDS中。未固化的固体SNEDDS药物释放可忽略不计(2小时后仅5%药物释放),而固化的S - SNEDDS与未固化的相比,在2小时时总药物释放提高了高达12倍。然而,固化的S - SNEDDS在加速条件下储存时显示出相当程度的CN降解和药物释放减少。

结论

所采用的固化方法提供了一种有前景的技术,可将吸附剂对药物释放的不利影响降至最低,并实现固化SNEDDS更好的药物释放。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4694/9863206/5fe3a6b21cab/pharmaceutics-15-00134-g001.jpg

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