Food Bioscience, Journal Year: 2024, Volume and Issue: 62, P. 105399 - 105399
Published: Nov. 2, 2024
Language: Английский
Food Bioscience, Journal Year: 2024, Volume and Issue: 62, P. 105399 - 105399
Published: Nov. 2, 2024
Language: Английский
International Journal of Nanomedicine, Journal Year: 2024, Volume and Issue: Volume 19, P. 8373 - 8400
Published: Aug. 1, 2024
Despite all major advancements in drug discovery and development the pharmaceutical industry, cancer is still one of most arduous challenges for scientific community. The implications nanotechnology have certainly resolved issues related to conventional anticancer modalities; however, undesired recognition nanoparticles (NPs) by mononuclear phagocyte system (MPS), their poor stability biological fluids, premature release payload, low biocompatibility restricted clinical translation. In recent decades, chitosan (CS)-based nanodelivery systems (eg, polymeric NPs, micelles, liposomes, dendrimers, conjugates, solid lipid nanoparticles, etc.) attained promising from researchers improving pharmacokinetics pharmacodynamics chemotherapeutics. However, specialty this review mainly focus on critically discuss targeting potential various CS-based NPs treatment different types cancer. Based delivery mechanisms, we classified into stimuli-responsive, passive, or active nanosystems. Moreover, functionalization strategies grafting with polyethylene glycol (PEG), hydrophobic substitution, tethering stimuli-responsive linkers, conjugation ligands) adapted architecture CS-NPs target-specific chemotherapeutics also been considered. Nevertheless, based therapeutics hold great promise therapeutic outcomes while mitigating off-target effects chemotherapeutics, a long-term safety profile testing humans are warranted successful
Language: Английский
Citations
7Journal of Materials Chemistry B, Journal Year: 2022, Volume and Issue: 10(44), P. 9125 - 9178
Published: Jan. 1, 2022
Chondroitin sulfate (CS), a natural anionic mucopolysaccharide, belonging to the glycosaminoglycan family, has been in limelight for its unique properties diverse biomedical applications.
Language: Английский
Citations
26Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: 100, P. 106050 - 106050
Published: Aug. 8, 2024
Language: Английский
Citations
5Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: 101, P. 106183 - 106183
Published: Sept. 11, 2024
Language: Английский
Citations
4International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 280, P. 135923 - 135923
Published: Sept. 23, 2024
Language: Английский
Citations
4International Journal of Nanomedicine, Journal Year: 2025, Volume and Issue: Volume 20, P. 991 - 1020
Published: Jan. 1, 2025
Owing to its high prevalence, colossal potential of chemoresistance, metastasis, and relapse, breast cancer (BC) is the second leading cause cancer-related fatalities in women. Several treatments (eg, chemotherapy, surgery, radiations, hormonal therapy, etc.) are conventionally prescribed for treatment BC; however, these associated with serious systemic aftermaths. In this research, we aimed design a multiprong targeting strategy concurrent action against different phenotypes BC (MCF-7 SK-BR-3) tumor-associated macrophages (TAMs) relapse-free BC. Paclitaxel (PTX) tamoxifen (TMX) co-loaded chitosan (CS) nanoparticles (NPs) were prepared using ionic-gelation method optimized Design Expert® software by controlling material attributes. For selective through CD44-receptors that heavily expressed on cells TAMs, fabricated NPs (PTX-TMX-CS-NPs) functionalized hyaluronic acid (HA) as ligand. The HA-PTX-TMX-CS-NPs exhibited desired physicochemical properties (PS ~230 nm, PDI 0.30, zeta ~21.5 mV), smooth spherical morphology, encapsulation efficiency (PTX ~72% TMX ~97%), good colloidal stability, biphasic release kinetics. Moreover, lowest cell viability depicted MCF-7 (~25%), SK-BR-3 (~20%), RAW 264.7 induction apoptosis, cycle arrest, enhanced internalization, alleviation migration proved superior anticancer compared unfunctionalized other control medicines. HA-functionalization promising CD44-receptors-mediated TAMs mitigate progression, relapse
Language: Английский
Citations
0Antibiotics, Journal Year: 2025, Volume and Issue: 14(2), P. 169 - 169
Published: Feb. 8, 2025
Background/Objectives: Pulmonary delivered tobramycin (TOB) is a standard treatment for Pseudomonas aeruginosa lung infections, that, along with Staphylococcus aureus, one of the most common bacteria causing recurring infections in CF patients. However, only available formulation on market containing tobramycin, TOBI®, sold at price that makes access to difficult. Therefore, this work focuses development and characterization an ionic complex between polyelectrolyte, hyaluronic acid (HA) its salt, sodium hyaluronate (NaHA), TOB be formulated as inhalable dry powder. Methods: The solid state obtained by spray drying technique was physicochemically characterized infrared spectroscopy, thermal analysis X-ray diffraction, confirming interaction both complexes. Results: powder density, geometric size, morphology aerodynamic performance showed suitable properties formulations reach deep lung. Moisture uptake found low, HA-TOB remaining unchanged, while NaHA-TOB required significant protection against humidity. biopharmaceutical vitro experiments rapid dissolution which can have positively impact reducing side effects, drug release study demonstrated reversible polyelectrolyte–drug interaction. Microbiological P. S. aureus improved bacterial growth inhibition bactericidal efficacy, well better eradication biofilms when compared TOB. Conclusions: A simple polyelectrolyte-drug represents promising strategy antimicrobial pulmonary delivery cystic fibrosis (CF) infections.
Language: Английский
Citations
0International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: unknown, P. 142486 - 142486
Published: March 1, 2025
Language: Английский
Citations
0AAPS PharmSciTech, Journal Year: 2025, Volume and Issue: 26(4)
Published: March 27, 2025
Language: Английский
Citations
0International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 270, P. 132269 - 132269
Published: May 12, 2024
Language: Английский
Citations
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