Oral Site-Specific Drug Delivery System: Functionalized Modified Hyaluronic Acid 5-Fluorouracil Microspheres for Colon Cancer

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
He Ying Mao, Jing Xu, Shuai Hong, Jing Shu Piao, Ming Guan Piao
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Abstract

Purpose

The study aimed to create functionalized modified 5-fluorouracil hyaluronic acid microspheres (PAR-HA Mps/5-Fu) for localized drug delivery to colorectal cancer by targeting the CD44 receptor, with the ability to control release rate by different PH release environments.

Methods

PAR-HA Mps/5-Fu were prepared by emulsification cross-linking method. The optimal oral formulation was identified through a combination of single-factor examination and orthogonal experimental design. In vitro release experiments were performed in different media and drug release models were fitted. The in vivo pharmacokinetic profile, in vivo safety, and in vivo biodistribution of PAR-HA Mps/5-Fu were investigated in in vivo examinations.

Results

In this study, PAR-HA Mps/5-Fu was successfully prepared. While PAR-HA Mps/5-Fu was difficult to dissolve (16.17%) in artificial gastric fluid, it was constantly released (98.45%) in artificial colonic fluid, and its release pattern fit the Weibull equation. The results of the in vivo experiments showed that PAR-HA Mps/5-Fu had good drug localization in the pathological environment, the pharmacokinetic parameters of the formulation showed significant improvement compared to the 5-FU solution. Meanwhile, oral administration of PAR-HA Mps/5-Fu did not affect the organism, tissues, or blood system.

Conclusion

The study demonstrated that PAR-HA Mps/5-FU can facilitate the local delivery of 5-FU to the colon, thereby addressing the clinical limitations of 5-FU, including its short plasma half-life, low bioavailability, and high toxicity.

Graphical Abstract

口服部位特异性给药系统:功能化修饰透明质酸5-氟尿嘧啶微球用于结肠癌
目的通过靶向CD44受体,制备功能化修饰的5-氟尿嘧啶透明质酸微球(PAR-HA Mps/5-Fu),并通过不同的PH释放环境控制其释放速度。方法采用乳化交联法制备spar - ha Mps/5-Fu。采用单因素试验和正交试验设计相结合的方法确定最佳口服配方。在不同介质中进行体外释放实验,并建立药物释放模型。通过体内试验研究了PAR-HA Mps/5-Fu的体内药动学特征、体内安全性和体内生物分布。结果本研究成功制备了PAR-HA Mps/5-Fu。PAR-HA Mps/5-Fu在人工胃液中难以溶解(16.17%),但在人工结肠液中持续释放(98.45%),其释放模式符合Weibull方程。体内实验结果表明,PAR-HA Mps/5-Fu在病理环境下具有良好的药物定位,与5-Fu溶液相比,该制剂的药代动力学参数有明显改善。同时,口服PAR-HA Mps/5-Fu对机体、组织或血液系统没有影响。结论研究表明,PAR-HA Mps/5-FU可促进5-FU在结肠的局部递送,从而解决了5-FU血浆半衰期短、生物利用度低、毒性大的临床局限性。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pharmaceutical Innovation
Journal of Pharmaceutical Innovation PHARMACOLOGY & PHARMACY-
CiteScore
3.70
自引率
3.80%
发文量
90
审稿时长
>12 weeks
期刊介绍: The Journal of Pharmaceutical Innovation (JPI), is an international, multidisciplinary peer-reviewed scientific journal dedicated to publishing high quality papers emphasizing innovative research and applied technologies within the pharmaceutical and biotechnology industries. JPI''s goal is to be the premier communication vehicle for the critical body of knowledge that is needed for scientific evolution and technical innovation, from R&D to market. Topics will fall under the following categories: Materials science, Product design, Process design, optimization, automation and control, Facilities; Information management, Regulatory policy and strategy, Supply chain developments , Education and professional development, Journal of Pharmaceutical Innovation publishes four issues a year.
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