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塞来昔布液体栓剂经直肠给药对大鼠具有更高的生物利用度和安全性

Rectal Administration of Celecoxib Liquid Suppositories with Enhanced Bioavailability and Safety in Rats.

作者信息

Jiao Yan, Xie Shijing, Baseer Abdul, Ud-Din Fakhar

机构信息

Department of Pharmacy, Cangzhou Medical College, Cangzhou, Hebei Province 061000, China.

Department of Pharmacy, Abasyn University Islamabad, Islamabad, Pakistan.

出版信息

Curr Drug Deliv. 2023;20(2):201-210. doi: 10.2174/1567201819666220513091015.

Abstract

BACKGROUND

Celecoxib is generally used for the treatment of rheumatoid arthritis, however its poor bioavailability and cytotoxicity in pure form have reduced its therapeutic efficacy. This study aims to develop celecoxib liquid suppositories with improved bioavailability and reduced toxicity.

METHODS

The celecoxib liquid suppositories were prepared by thoroughly mixing celecoxib, poloxamer 188 and poloxamer 407, and tween-20, respectively used as drug, polymers and surfactant, in triple distilled water using cold technique. The developed liquid suppositories were characterized in terms of their gelation temperature, gelation time, and gel strength. Moreover, the muco-adhesive force was determined for the suppositories. The release behavior of the liquid suppositories was investigated in distilled water and compared with drug suspension. Furthermore, pharmacokinetics and morphological studies were carried out in rats after rectal administration of the celecoxib liquid suppository compared with drug suspension.

RESULTS

Poloxamer 188 and Tween-20 concentrations have significantly reduced the gelation temperature and time; however, the gel strength and bio-adhesive force were significantly enhanced. The concentration of celecoxib has no significant effect on the properties of liquid suppositories. A significantly enhanced and potentially sustained drug release was observed from the celecoxib liquid suppositories as compared with the drug suspension. The optimized formulation was easy to administer rectally because it quickly forms gel upon insertion into the body due to a suitable gelation temperature of about 31.7 °C. After rectal administration in rats, the celecoxib liquid suppository gave a significantly increased pharmacokinetic profile including enhanced plasma concentration and 9.7 fold improved area under the curve (AUC) compared to the drug suspension. Additionally, the morphology study exhibited no toxicity to the rectal tissue, no signs of irritation, or injury after the application of suppository. However, severe rectal tissue toxicity and irritation was observed in the suspension treated rectum.

CONCLUSION

It can be concluded that the liquid suppository system may significantly enhance the solubilization and bio-availability of sparingly water-soluble drugs as evident in the case of celecoxib with no toxicity at the site of application.

摘要

背景

塞来昔布通常用于治疗类风湿性关节炎,然而其纯形式的生物利用度差和细胞毒性降低了其治疗效果。本研究旨在开发具有改善的生物利用度和降低毒性的塞来昔布液体栓剂。

方法

通过将塞来昔布、泊洛沙姆188和泊洛沙姆407以及吐温-20分别用作药物、聚合物和表面活性剂,采用冷技术在重蒸馏水中充分混合来制备塞来昔布液体栓剂。对所开发的液体栓剂进行凝胶化温度、凝胶化时间和凝胶强度方面的表征。此外,测定栓剂的粘膜粘附力。在蒸馏水中研究液体栓剂的释放行为,并与药物悬浮液进行比较。此外,与药物悬浮液相比,在大鼠直肠给药塞来昔布液体栓剂后进行药代动力学和形态学研究。

结果

泊洛沙姆188和吐温-20的浓度显著降低了凝胶化温度和时间;然而,凝胶强度和生物粘附力显著增强。塞来昔布的浓度对液体栓剂的性质没有显著影响。与药物悬浮液相比,观察到塞来昔布液体栓剂的药物释放显著增强且可能持续。优化后的制剂易于直肠给药,因为由于合适的凝胶化温度约为31.7°C,它在插入体内后会迅速形成凝胶。在大鼠直肠给药后,与药物悬浮液相比,塞来昔布液体栓剂的药代动力学特征显著增加,包括血浆浓度升高和曲线下面积(AUC)提高9.7倍。此外,形态学研究表明,应用栓剂后对直肠组织无毒性、无刺激或损伤迹象。然而,在悬浮液处理的直肠中观察到严重的直肠组织毒性和刺激。

结论

可以得出结论,液体栓剂系统可能显著提高难溶性药物的溶解度和生物利用度,如塞来昔布的情况所示,在应用部位无毒性。

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