生物chanin-A共晶体制剂提高了生物利用度,并通过减轻炎症改善了脑磷脂诱发的胰腺炎。

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Hari Priya Sripadi , Rajwinder Kaur , Saylee Manohar Koli , Nidhi Sharma , Vijaya Sarathi U.V.R. , Jagadeesh Babu Nanubolu , Sai Balaji Andugulapati , Ramakrishna Sistla
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引用次数: 0

摘要

将治疗成分与适当的共形成剂进行共结晶是一种强大的技术,可增强活性药物成分(APIs)的物理化学和药代动力学特性及有效性。生物黄酮 A(BCA)是一种具有药用潜力的黄酮类化合物,但其溶解性差,口服生物利用度低。本研究旨在设计和开发一种新型 BCA-烟酰胺共晶体作为 BCC,以提高 BCA 的口服生物利用度,并通过利用组织/血清代谢物图谱阐明目标识别,探索其在改善脑磷脂诱导的急性胰腺炎(CIAP)方面的治疗潜力。该共晶体是通过超分子合成方法设计的,并通过单晶 X 射线衍射进行了表征,证实晶体中 BCA 和烟酰胺(NCT)形成了稳固的三维氢键网络。傅立叶变换红外光谱(FT-IR)和 DSC 用于分析共晶体的分子间相互作用和热行为。与单独的 BCA 相比,BCC 表现出更强的溶解性和药物释放性,从而提高了口服生物利用度和胰腺组织浓度。在CIAP模型中,将BCC与BCA进行比较,BCC疗法明显减轻了脑磷脂诱发的胰腺炎,这体现在胰腺组织的炎症、胰腺细胞萎缩和淀粉酶水平显著降低。此外,共晶制剂还能下调氧化应激标记物、炎症细胞因子和巨噬细胞相关蛋白。该研究借助 Orbitrap Exploris 质谱仪确定了与 AP 相关的独特代谢组学特征,这为开发重点诊断工具以改善预后铺平了道路。总之,这些结果为探索与特定生物标志物相关的机理途径提供了新的见解,并强调了 BCC 共晶体是提高 BCA 治疗潜力的一种有前途的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Biochanin-A co-crystal formulation improves bioavailability and ameliorates cerulein-induced pancreatitis by attenuating the inflammation

Biochanin-A co-crystal formulation improves bioavailability and ameliorates cerulein-induced pancreatitis by attenuating the inflammation
Co-crystallization of a therapeutic ingredient with an appropriate co-former is a powerful technique to augment the physicochemical and pharmacokinetic properties and the effectiveness of Active Pharmaceutical Ingredients (APIs). Biochanin A (BCA), a flavonoid with medicinal potential, is limited by poor solubility and low oral bioavailability. This study aimed to design and develop a novel BCA-nicotinamide cocrystal as BCC to enhance BCA’s oral bioavailability and explore its therapeutic potential for ameliorating cerulein-induced acute pancreatitis (CIAP) by elucidating the target identification utilizing tissue/serum metabolite profiles. The cocrystal was designed by the supramolecular synthon approach and characterized by single-crystal X-ray diffraction that confirms a robust three-dimensional hydrogen-bonded network of BCA and Nicotinamide (NCT) in the crystal. FT-IR and DSC were used to analyze the cocrystal’s intermolecular interactions and thermal behavior. BCC exhibited enhanced solubility and drug release compared to BCA alone, resulting in enhanced oral bioavailability and pancreatic tissue concentration. Comparing BCC to BCA in the CIAP model, BCC therapy remarkably reduced cerulein-induced pancreatitis, evidenced by significant reductions in inflammation, acinar cell atrophy, and amylase levels in pancreatic tissues. Further, the cocrystal formulation also down-regulated the oxidative stress markers, inflammatory cytokines and macrophage-related proteins. The study has identified distinct metabolomic signatures linked with AP with the help of Orbitrap Exploris mass spectrometry, which could pave the way for creating focused diagnostic tools for a better prognosis. In conclusion, these results offer new insights into exploring mechanistic pathways associated with specific biomarkers and underscore BCC cocrystal as a promising approach to enhance BCA’s therapeutic potential.
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来源期刊
CiteScore
10.70
自引率
8.60%
发文量
951
审稿时长
72 days
期刊介绍: The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
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