直肠给药塞来昔布液体栓剂提高大鼠生物利用度和安全性。

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY Current drug delivery Pub Date : 2023-01-01 DOI:10.2174/1567201819666220513091015
Yan Jiao, Shijing Xie, Abdul Baseer, Fakhar Ud-Din
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引用次数: 6

摘要

背景:塞来昔布通常用于类风湿性关节炎的治疗,但其较差的生物利用度和纯形式的细胞毒性降低了其治疗效果。本研究旨在开发具有提高生物利用度和降低毒性的塞来昔布液体栓剂。方法:将塞来昔布、泊洛沙姆188、泊洛沙姆407、吐温-20分别作为药物、聚合物和表面活性剂,在三倍蒸馏水中采用冷法制备塞来昔布液体栓剂。对所研制的液体栓剂进行了凝胶温度、凝胶时间和凝胶强度的表征。并测定了栓剂的黏附力。考察了液体栓剂在蒸馏水中的释放行为,并与药物悬浮液进行了比较。此外,对塞来昔布液体栓剂直肠给药后大鼠进行了药代动力学和形态学研究,并与药物悬浮液进行了比较。结果:poloxam188和Tween-20浓度显著降低了凝胶温度和凝胶时间;但凝胶强度和生物粘附力明显增强。塞来昔布的浓度对液体栓剂的性质无显著影响。与药物悬浮液相比,塞来昔布液体栓剂的药物释放明显增强,并且可能持续释放。优化后的配方易于直肠给药,因为它在插入体内后迅速形成凝胶,因为合适的凝胶温度约为31.7℃。在大鼠直肠给药后,塞来昔布液体栓剂的药代动力学特征显著增加,包括血浆浓度增强,曲线下面积(AUC)比药物悬浮液提高9.7倍。此外,形态学研究显示栓剂应用后对直肠组织无毒性,无刺激或损伤迹象。然而,在处理后的悬浮液中观察到严重的直肠组织毒性和刺激。结论:液体栓剂系统可显著提高非水溶性药物的增溶性和生物利用度,塞来昔布在用药部位无毒性。
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Rectal Administration of Celecoxib Liquid Suppositories with Enhanced Bioavailability and Safety in Rats.

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.

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来源期刊
Current drug delivery
Current drug delivery PHARMACOLOGY & PHARMACY-
CiteScore
5.10
自引率
4.20%
发文量
170
期刊介绍: Current Drug Delivery aims to publish peer-reviewed articles, research articles, short and in-depth reviews, and drug clinical trials studies in the rapidly developing field of drug delivery. Modern drug research aims to build delivery properties of a drug at the design phase, however in many cases this idea cannot be met and the development of delivery systems becomes as important as the development of the drugs themselves. The journal aims to cover the latest outstanding developments in drug and vaccine delivery employing physical, physico-chemical and chemical methods. The drugs include a wide range of bioactive compounds from simple pharmaceuticals to peptides, proteins, nucleotides, nucleosides and sugars. The journal will also report progress in the fields of transport routes and mechanisms including efflux proteins and multi-drug resistance. The journal is essential for all pharmaceutical scientists involved in drug design, development and delivery.
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