One-step lipid–polymeric hybrid nanoparticles as intracanal drug delivery system: Synthesis, characterization, antimicrobial activity, and dentinal penetration

IF 4.3 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Ahmad AlMukhallalati, Amal Yousfan, Diego Hidalgo-Martínez, Samer Ibrahim, Khitam Al Moarrawi, Abdulsamie Hanano
{"title":"One-step lipid–polymeric hybrid nanoparticles as intracanal drug delivery system: Synthesis, characterization, antimicrobial activity, and dentinal penetration","authors":"Ahmad AlMukhallalati,&nbsp;Amal Yousfan,&nbsp;Diego Hidalgo-Martínez,&nbsp;Samer Ibrahim,&nbsp;Khitam Al Moarrawi,&nbsp;Abdulsamie Hanano","doi":"10.1016/j.nano.2026.102979","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>This study developed two lipid–polymeric hybrid nanoparticle thermosensitive gels, hypothesizing enhanced physicochemical properties, antimicrobial efficacy, and dentinal penetration compared to free drugs.</div></div><div><h3>Methods</h3><div>Ciprofloxacin-loaded lecithin–PLGA nanoparticles (CIP-LPNPs) and chitosan–lecithin nanoparticles (CS-LNPs) were synthesized via nanoprecipitation and characterized by DLS, SEM, FTIR and HPLC. Antimicrobial activity against <em>Enterococcus faecalis</em>, <em>Escherichia coli</em> and <em>Pseudomonas aeruginosa</em> was assessed by disk diffusion, MIC and biofilm assays; dentinal penetration of FITC-labeled CS-LNPs was evaluated by confocal microscopy.</div></div><div><h3>Results</h3><div>CIP-LPNPs and CS-LNPs measured 140.6 and 130.9 nm with zeta potentials of −29.4 and +28.9 mV, respectively. CIP-LPNPs showed 55.7% encapsulation and biphasic release. Both nanoparticles enhanced biofilm eradication against all strains; CS-LNPs exhibited two-fold lower MICs and significantly deeper tubular penetration than free chitosan (<em>p</em> &lt; 0.0001).</div></div><div><h3>Conclusions</h3><div>Both CIP-LPNPs and CS-LNPs improved physicochemical and antibiofilm properties over their free drugs; however, as no biocompatibility assessment was performed, these formulations cannot be considered safe without such validation.</div></div>","PeriodicalId":19050,"journal":{"name":"Nanomedicine : nanotechnology, biology, and medicine","volume":"75 ","pages":"Article 102979"},"PeriodicalIF":4.3000,"publicationDate":"2026-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanomedicine : nanotechnology, biology, and medicine","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1549963426000808","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/6/16 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction

This study developed two lipid–polymeric hybrid nanoparticle thermosensitive gels, hypothesizing enhanced physicochemical properties, antimicrobial efficacy, and dentinal penetration compared to free drugs.

Methods

Ciprofloxacin-loaded lecithin–PLGA nanoparticles (CIP-LPNPs) and chitosan–lecithin nanoparticles (CS-LNPs) were synthesized via nanoprecipitation and characterized by DLS, SEM, FTIR and HPLC. Antimicrobial activity against Enterococcus faecalis, Escherichia coli and Pseudomonas aeruginosa was assessed by disk diffusion, MIC and biofilm assays; dentinal penetration of FITC-labeled CS-LNPs was evaluated by confocal microscopy.

Results

CIP-LPNPs and CS-LNPs measured 140.6 and 130.9 nm with zeta potentials of −29.4 and +28.9 mV, respectively. CIP-LPNPs showed 55.7% encapsulation and biphasic release. Both nanoparticles enhanced biofilm eradication against all strains; CS-LNPs exhibited two-fold lower MICs and significantly deeper tubular penetration than free chitosan (p < 0.0001).

Conclusions

Both CIP-LPNPs and CS-LNPs improved physicochemical and antibiofilm properties over their free drugs; however, as no biocompatibility assessment was performed, these formulations cannot be considered safe without such validation.

Abstract Image

一步脂质-聚合物杂化纳米颗粒作为肛管内给药系统:合成、表征、抗菌活性和牙本质渗透。
本研究开发了两种脂质-聚合物杂化纳米颗粒热敏凝胶,假设与游离药物相比,其物理化学性能、抗菌功效和牙本质穿透性都有所提高。方法:采用纳米沉淀法合成环丙沙星负载的卵磷脂- plga纳米颗粒(cip - lnps)和壳聚糖-卵磷脂纳米颗粒(CS-LNPs),并采用DLS、SEM、FTIR和HPLC对其进行表征。采用纸片扩散法、MIC法和生物膜法检测对粪肠球菌、大肠杆菌和铜绿假单胞菌的抑菌活性;用共聚焦显微镜观察fitc标记的CS-LNPs的牙本质渗透情况。结果:cip - lnps和CS-LNPs的波长分别为140.6和130.9 nm, zeta电位分别为-29.4和+28.9 mV。cip - lnps包封率为55.7%,双相释放。这两种纳米颗粒都增强了对所有菌株的生物膜根除;与游离壳聚糖相比,CS-LNPs的mic低两倍,管状穿透深度也明显加深(p )。结论:cip - lnp和CS-LNPs的理化性能和抗生物膜性能都优于游离壳聚糖;然而,由于没有进行生物相容性评估,没有这样的验证,这些配方不能被认为是安全的。
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
CiteScore
11.10
自引率
0.00%
发文量
133
审稿时长
42 days
期刊介绍: The mission of Nanomedicine: Nanotechnology, Biology, and Medicine (Nanomedicine: NBM) is to promote the emerging interdisciplinary field of nanomedicine. Nanomedicine: NBM is an international, peer-reviewed journal presenting novel, significant, and interdisciplinary theoretical and experimental results related to nanoscience and nanotechnology in the life and health sciences. Content includes basic, translational, and clinical research addressing diagnosis, treatment, monitoring, prediction, and prevention of diseases.
×
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
小红书