Pulmonary delivery of anti-tuberculosis drugs has emerged as a promising alternative for increasing local drug concentrations whilst minimising side effects. Natural polymers—polysaccharides capable of forming polyelectrolyte complexes (PECs) through electrostatic interactions—show great promise in this field. In this study, mucoadhesive chitosan-gellan gum nanoparticles were developed for the controlled release of isoniazid using the polyelectrolyte complex coacervation method. Parameters such as the chitosan-to-gellan gum ratio and the medium pH were investigated to achieve suitable particle size, polydispersity, surface charge, drug loading and encapsulation efficiency. The morphology of the produced nanoparticles was determined using transmission electron microscopy (TEM) and nanoparticle tracking analysis (NTA), which confirmed the formation of nanoscale spherical particles. The mucoadhesive properties were tested on ovine lung tissue using fluorescence retention analysis, whilst in vitro drug release was studied under physiological conditions. Antimycobacterial activity against Mycobacterium tuberculosis H37Rv was assessed using the Mycobacteria Growth Indicator Tube (MGIT) system, followed by subculturing on Löwenstein–Jensen medium. The produced nanoparticles exhibited high mucoadhesion, maintaining prolonged retention on lung tissue. Drug release showed an initial burst followed by sustained release over 24 h. These results demonstrate that CSGG–INH nanoparticles possess sustained drug release, good mucoadhesion to the lungs and high antimycobacterial activity, supporting their further development as potential carriers for pulmonary delivery of anti-tuberculosis drugs.
This study showed that mucoadhesive polymeric nanoparticles of vonoprazan significantly enhanced solubility, pH-dependent release, and improved mucoadhesion, making it a promising approach to improve the oral bioavailability of drugs with poor water solubility.
S. Sajjad, U. Tulain, M. Asim et al.· International Journal of Nan...· 0 citations
These findings demonstrate that the combination of green fabrication, controlled Ibuprofen release, good biocompatibility, and antimicrobial efficacy highlights the potential of these biocomposite microparticles as innovative hybrid nanostructures that can significantly improve therapeutic outcomes.
D. Rață, Gisela Trifas, R. Șomoghi et al.· Polymers· 0 citations
The developed chitosan-coated Eudragit® S100 nanoparticle system represents a promising platform for sustained, colon-targeted oral delivery of HSP and other poorly bioavailable bioactive compounds.
Gliclazide-loaded chitosan–sodium alginate microspheres were developed by ionic gelation to obtain sustained oral drug release. Six formulations (F1–F6) were prepared by varying polymer concentrations while maintaining gliclazide, sodium tripolyphosphate and Tween 80 levels constant. The microspheres were characterized...
K. B., E. J., Perumal P et al.· International journal of pha...· 0 citations
Development of an injectable and in-situ curable elastomeric nanohybrid, synthesized from a functionalized polyalphaolefin resin (ACPAO) and methacrylate-modified chitosan (MACS) nanofiller, and utilized for the drug delivery of Naproxen.
Somayyeh Sadat Afi Kheljani, M. Nekoomanesh-Haghighi, M. Atai et al.· International Journal of Bio...· 0 citations
Background: Fungal infections remain a significant therapeutic challenge due to recurrence, limited treatment options, and reduced susceptibility to conventional antifungal agents. Allicin, a natural organosulfur compound, possesses promising antifungal activity but requires an appropriate delivery system for effective...
K. J· Natural Resources for Human...· 0 citations
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