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质量源于设计(QbD)引导的磷脂标记纳米化乳香酸脂质体递送用于类风湿性关节炎的有效治疗

QbD-guided phospholipid-tagged nanonized boswellic acid naturosomal delivery for effective rheumatoid arthritis treatment.

作者信息

Usapkar Poonam, Saoji Suprit, Jagtap Pradnya, Ayyanar Muniappan, Kalaskar Mohan, Gurav Nilambari, Nadaf Sameer, Prasad Satyendra, Laloo Damiki, Khan Mohd Shahnawaz, Chikhale Rupesh, Gurav Shailendra

机构信息

Department of Pharmacognosy, Goa College of Pharmacy, Panaji, Goa University, Goa-403 001, India.

Department of Pharmaceutical Sciences, R. T. M. Nagpur University, Nagpur, Maharashtra- 440 033, India.

出版信息

Int J Pharm X. 2024 May 19;7:100257. doi: 10.1016/j.ijpx.2024.100257. eCollection 2024 Jun.

Abstract

Studies have reported the potential role of Boswellic acids (BAs), bioactive pentacyclic triterpenes from (BS), in treating rheumatoid arthritis (RA). However, poor water solubility and limited oral absorption are restricting factors for its better therapeutic efficacy. Based on these assumptions, the current study aimed to develop naturosomal delivery of BAs to boost their extremely low bioavailability, colloidal stability, and water solubility. Nanonized naturosomes were developed and subsequently analyzed to show their physicochemical and functional features employing the quality-by-design approach. The solubility analysis of Boswellic acid naturosomes revealed a 16 times improvement in aqueous solubility compared to BS extract (BSE). The zeta potential and dynamic light scattering findings of BSE naturosomes (BSENs) have demonstrated their colloidal stability with regulated nano-size particles. Additionally, compared to BSE (⁓31%), dissolution experiments showed that >99% of pentacyclic triterpenes were released from BSENs. Studies on permeation showed that BSENs' permeation (>79%) significantly improved over BSE's (⁓20%). efficacy studies using CFA-prompted arthritis in rodents showed a critical expansion in body wt and an undeniable reduction in paw thickness, paw volume, and TNF-α treated with BSEN compared to the arthritis control and BSE-treated group. These findings suggest that BSENs can help treat RA drugs by demonstrating their efficacy in further clinical research to validate the significant improvements.

摘要

研究报告了乳香酸(BAs),一种来自乳香(BS)的生物活性五环三萜,在治疗类风湿性关节炎(RA)中的潜在作用。然而,水溶性差和口服吸收有限是其获得更好治疗效果的限制因素。基于这些假设,本研究旨在开发乳香酸的纳米脂质体递送系统,以提高其极低的生物利用度、胶体稳定性和水溶性。制备了纳米化的纳米脂质体,随后采用质量源于设计的方法对其进行分析,以展示其物理化学和功能特性。乳香酸纳米脂质体的溶解度分析显示,与乳香提取物(BSE)相比,其水溶性提高了16倍。BSE纳米脂质体(BSENs)的zeta电位和动态光散射结果表明,其具有胶体稳定性,且颗粒尺寸可控。此外,与BSE(约31%)相比,溶出实验表明,超过99%的五环三萜从BSENs中释放出来。渗透研究表明,BSENs的渗透率(>79%)比BSE(约20%)有显著提高。使用佐剂性关节炎大鼠模型进行的药效学研究表明,与关节炎对照组和BSE治疗组相比,用BSEN治疗的大鼠体重显著增加,爪厚度、爪体积和TNF-α显著降低。这些发现表明,BSENs在进一步的临床研究中证实了其显著改善效果,有助于治疗类风湿性关节炎药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/372b/11637072/e221647b6667/ga1.jpg

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