2015
DOI: 10.1016/j.ijpharm.2015.09.055
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Preparation and evaluation of lipid polymer nanoparticles for eradicating H. pylori biofilm and impairing antibacterial resistance in vitro

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Cited by 77 publications
(36 citation statements)
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“…Using this one-step method, Cai et al [80] used Pylori adhesion material pectin sulfate (PECS) as the polymer and rhamnolipid as the lipid to encapsulate amoxicillin; the particle size was 200 nm. In addition, Li et al [81] employed curcumin–PLGA as the polymer, and 1,2-dipalmitoyl- sn -glycero-3-phosphocholine (DPPC) and DSPE-PEG as the lipids to entrap human fibronectin, and the particle size was ~150 nm.…”
Section: Methods For Preparing Drug Carriersmentioning
confidence: 99%
“…Using this one-step method, Cai et al [80] used Pylori adhesion material pectin sulfate (PECS) as the polymer and rhamnolipid as the lipid to encapsulate amoxicillin; the particle size was 200 nm. In addition, Li et al [81] employed curcumin–PLGA as the polymer, and 1,2-dipalmitoyl- sn -glycero-3-phosphocholine (DPPC) and DSPE-PEG as the lipids to entrap human fibronectin, and the particle size was ~150 nm.…”
Section: Methods For Preparing Drug Carriersmentioning
confidence: 99%
“…Table 4 gives a summary of lipid‐based NPs for antimicrobial drug delivery. Cai et al reported a new lipid polymer nanoparticle formulation with rhamnolipid and phospholipids as the outer mixed lipids layer (RHL‐PC‐LPN) ( Figure ) . Amoxicillin (AMX) (10.2%) and an anti H. pylori adhesion material pectin sulfate (PECS) were loaded into the LPNs to facilitate the disruption of H. pylori biofilms and further enhanced their susceptibility to antibacterial agents.…”
Section: Classification Of Antimicrobial Nanoparticlesmentioning
confidence: 99%
“…Additionally, the use of nanotechnology provides important improvements in the pharmacokinetics of antibiotics whose application is limited due to low solubility, poor bioavailability after oral administration, short half-life, high toxicity or instability in physiological conditions ( Figure 1) [8][9][10]. A broad spectrum of antimicrobial activity described for a variety of nanomaterials supports the idea that the employment of antibiotic-conjugated nanoformulations will provide a more efficient way to overcome the ever-growing drug resistance of pathogens [11,12].…”
Section: Introductionmentioning
confidence: 95%
“…Jamil et al demonstrated that cefazolin-loaded chitosan nanoparticles can be employed as stable and effective agents against multidrug-resistant Klebsiella pneumoniae, Pseudomonas aeruginosa and extended spectrum beta lactamase (ESBL) positive E. coli [11]. Novel studies performed by Cai et al revealed that the treatment of H. pylori with amoxicillin and pectin sulfate-loaded lipid PNPs significantly eradicates H. pylori in the biofilm form, inhibits bacteria from adhering to gastric cells and decreases the MIC value for amoxicillin, which increases its ability to inhibit bacterial colonization despite the well-known resistance of H. pylori to antimicrobial treatment [12]. Additionally, Hussein-Al-Ali et al reported strong antimicrobial potential of streptomycin-conjugated magnetic nanoparticles coated with chitosan against drug-sensitive S. aureus and its methicillin-resistant counterpart (MRSA), which might be a promising strategy to fight drug-resistant infections, particularity those reported in the hospital environment [46].…”
Section: Recent Advances In Application Of Antibioticconjugated Nanopmentioning
confidence: 99%