Mesoporous polymeric nanoparticles for effective treatment of inflammatory diseases: an in vivo study†

IF 6.1 3区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS
Divya Pareek, Md. Zeyaullah, Sukanya Patra, Oviya Alagu, Gurmeet Singh, Kirti Wasnik, Prem Shankar Gupta and Pradip Paik
{"title":"Mesoporous polymeric nanoparticles for effective treatment of inflammatory diseases: an in vivo study†","authors":"Divya Pareek, Md. Zeyaullah, Sukanya Patra, Oviya Alagu, Gurmeet Singh, Kirti Wasnik, Prem Shankar Gupta and Pradip Paik","doi":"10.1039/D4TB02012J","DOIUrl":null,"url":null,"abstract":"<p >Acute inflammatory diseases require suitable medicine over the existing therapeutics. In this line, the present work is focused on developing polymeric nanomedicine for the treatment of inflammatory disorders. Herein, cell viable nanoparticles (GlyNPs) of size 180–250 nm in diameter and pore size of 4–5 nm in diameter, based on glycine and acryloyl chloride, have been developed and proved to be a potential anti-inflammatory agent without using any conventional drugs. These particles exhibit colloidal stability (with a zeta potential of −35.6 mV). A network pharmacology-based computational study has been executed on 9076 genes and proteins responsible for inflammatory diseases, out of which 10 are selected that have a major role in rheumatoid arthritis (RA). <em>In silico</em> docking study has been conducted to find out the targeted efficiency of the GlyNPs considering 10 inflammation-specific markers, namely IL-6, IL-1β, TNF-α, TLR-4, STAT-1, MAPK-8, MAPK-14, iNOS, NF-κβ and COX-2. The results revealed that the GlyNPs could be an excellent anti-inflammatory component similar to aspirin. The <em>in vitro</em> inflammation activity of these GlyNPs has also been checked on an inflammation model generated by LPS in RAW 264.7 macrophages. Then, the <em>in vitro</em> anti-inflammation efficiency has been checked with 10–150 μg mL<small><sup>−1</sup></small> of GlyNP doses. The treatment efficiency has been checked on inflammation-responsible immune markers (NO level, NF-κβ, INF-γ, IL-6, IL-10, and TNF-α) and it was found that the GlyNPs are an excellent component in reducing inflammation. The <em>in vivo</em> therapeutic response of GlyNPs on the induced rheumatoid arthritis (RA) model has been evaluated by measuring the morphological, biochemical and immune-cytokine and interferon levels responsible for the inflammation, using a 2 g kg<small><sup>−1</sup></small> dose (sample to weight of rat). The anti-inflammatory efficiency of GlyNPs without using additional drugs was found to be excellent. Thus, GlyNPs could be paramount for the potential treatment of various inflammatory diseases.</p>","PeriodicalId":83,"journal":{"name":"Journal of Materials Chemistry B","volume":" 9","pages":" 3094-3113"},"PeriodicalIF":6.1000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry B","FirstCategoryId":"1","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/tb/d4tb02012j","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

Abstract

Acute inflammatory diseases require suitable medicine over the existing therapeutics. In this line, the present work is focused on developing polymeric nanomedicine for the treatment of inflammatory disorders. Herein, cell viable nanoparticles (GlyNPs) of size 180–250 nm in diameter and pore size of 4–5 nm in diameter, based on glycine and acryloyl chloride, have been developed and proved to be a potential anti-inflammatory agent without using any conventional drugs. These particles exhibit colloidal stability (with a zeta potential of −35.6 mV). A network pharmacology-based computational study has been executed on 9076 genes and proteins responsible for inflammatory diseases, out of which 10 are selected that have a major role in rheumatoid arthritis (RA). In silico docking study has been conducted to find out the targeted efficiency of the GlyNPs considering 10 inflammation-specific markers, namely IL-6, IL-1β, TNF-α, TLR-4, STAT-1, MAPK-8, MAPK-14, iNOS, NF-κβ and COX-2. The results revealed that the GlyNPs could be an excellent anti-inflammatory component similar to aspirin. The in vitro inflammation activity of these GlyNPs has also been checked on an inflammation model generated by LPS in RAW 264.7 macrophages. Then, the in vitro anti-inflammation efficiency has been checked with 10–150 μg mL−1 of GlyNP doses. The treatment efficiency has been checked on inflammation-responsible immune markers (NO level, NF-κβ, INF-γ, IL-6, IL-10, and TNF-α) and it was found that the GlyNPs are an excellent component in reducing inflammation. The in vivo therapeutic response of GlyNPs on the induced rheumatoid arthritis (RA) model has been evaluated by measuring the morphological, biochemical and immune-cytokine and interferon levels responsible for the inflammation, using a 2 g kg−1 dose (sample to weight of rat). The anti-inflammatory efficiency of GlyNPs without using additional drugs was found to be excellent. Thus, GlyNPs could be paramount for the potential treatment of various inflammatory diseases.

Abstract Image

介孔聚合物纳米颗粒有效治疗炎症性疾病:一项体内研究
急性炎症性疾病需要比现有治疗方法更合适的药物。在这方面,目前的工作重点是开发用于治疗炎症性疾病的聚合物纳米药物。本文以甘氨酸和丙烯酰氯为基础,开发了直径180-250 nm、孔径4-5 nm的细胞活性纳米颗粒(GlyNPs),并证明了它是一种潜在的抗炎剂,无需使用任何常规药物。这些粒子具有胶体稳定性(zeta电位为-35.6 mV)。一项基于网络药理学的计算研究已经对9076个与炎症疾病有关的基因和蛋白质进行了研究,其中10个被选中在类风湿性关节炎(RA)中起主要作用。在硅对接研究中,我们考虑了10种炎症特异性标志物,即IL-6、IL-1β、TNF-α、TLR-4、STAT-1、MAPK-8、MAPK-14、iNOS、NF-κβ和COX-2,来研究GlyNPs的靶向效率。结果表明,GlyNPs可能是一种类似于阿司匹林的极好的抗炎成分。这些GlyNPs的体外炎症活性也通过LPS在RAW 264.7巨噬细胞中产生的炎症模型进行了检测。以10 ~ 150 μg mL-1 GlyNP为剂量,观察其体外抗炎效果。通过对炎症相关免疫指标(NO水平、NF-κβ、INF-γ、IL-6、IL-10、TNF-α)的检测,发现GlyNPs具有良好的消炎作用。GlyNPs对类风湿关节炎(RA)模型的体内治疗反应通过测量形态学、生化、免疫细胞因子和干扰素水平进行了评估,使用2g kg-1剂量(样品比大鼠体重)。发现GlyNPs在不使用额外药物的情况下具有良好的抗炎效果。因此,GlyNPs可能对各种炎症性疾病的潜在治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Materials Chemistry B
Journal of Materials Chemistry B MATERIALS SCIENCE, BIOMATERIALS-
CiteScore
11.50
自引率
4.30%
发文量
866
期刊介绍: Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C.Journal of Materials Chemistry B is a Transformative Journal and Plan S compliant. Example topic areas within the scope of Journal of Materials Chemistry B are listed below. This list is neither exhaustive nor exclusive: Antifouling coatings Biocompatible materials Bioelectronics Bioimaging Biomimetics Biomineralisation Bionics Biosensors Diagnostics Drug delivery Gene delivery Immunobiology Nanomedicine Regenerative medicine & Tissue engineering Scaffolds Soft robotics Stem cells Therapeutic devices
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信