Fabrication of Mastic Gum Resin Tethered Phospholipid Nanocarriers for the Evaluation and Enhancement of Anti-inflammatory and Anti-bacterial Effects.

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY Current pharmaceutical design Pub Date : 2025-01-01 DOI:10.2174/0113816128353794241225083428
Karthikeyan Selvaraj, Sang-Jin Lee, Keun-Bae Song, Bong-Kyu Yoo, Arjunan Karuppaiah
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Abstract

Introduction: The objective of the present study was to improve the anti-inflammatory and antibacterial activities of mastic gum resin (MGR). MGR was loaded into a phospholipid nanocarrier with or without partially hydrolyzed ginsenoside, followed by dispersion into distilled water.

Methods: The phospholipid nanocarrier dispersion showed significantly enhanced in vitro release, porcine skin/ intestine permeation, and retention. When the ratio of the MGR versus partially hydrogenated ginsenoside reached 1:1 w/w in the nanocarrier composition, the in vitro release increased 54.8-fold compared to the MGR powder suspended in the release media.

Results: Permeation of the nanocarrier dispersion through the porcine skin and intestine increased 160-fold and 42-fold, respectively, compared to permeation of the MGR powder suspension. Furthermore, the nanocarrier dispersion reduced NO production and iNOS mRNA expression in the LPS-stimulated RAW264.7 cells. MIC and MBC of the nanocarrier dispersion against P. gingivalis were 4.11 ± 1.17 and 8.22 ± 2.35 μg/mL, respectively.

Conclusion: In conclusion, the anti-inflammatory and antibacterial activities of MGR were remarkably enhanced when the MGR was loaded into the nanocarrier with partially hydrolyzed ginsenoside.

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乳胶树脂系链磷脂纳米载体的制备及其抗炎、抗菌效果的评价与增强。
前言:本研究的目的是提高乳香胶树脂(MGR)的抗炎和抗菌活性。MGR被装载到有或没有部分水解人参皂苷的磷脂纳米载体中,然后分散到蒸馏水中。方法:磷脂纳米载体在体外释放、猪皮/肠渗透和滞留方面表现出明显增强。当MGR与部分氢化人参皂苷在纳米载体组成中的比例达到1:1 w/w时,MGR粉的体外释放量比悬浮在释放介质中的MGR粉提高了54.8倍。结果:与MGR粉混悬液相比,纳米载体分散体通过猪皮肤和肠道的渗透率分别提高了160倍和42倍。此外,纳米载体分散降低了lps刺激的RAW264.7细胞中NO的产生和iNOS mRNA的表达。纳米载体对牙龈卟啉单胞菌的MIC和MBC分别为4.11±1.17和8.22±2.35 μg/mL。结论:经部分水解人参皂苷负载于纳米载体后,MGR的抗炎抑菌活性明显增强。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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