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Palabras clave – provistas por la editorial

poly(lactic-co-glycolic acid) (PLGA); blood–brain barrier (BBB); current Good Manufacturing Practice (cGMP); Food and Drug Administration (FDA); nanotechnology; PLGA nanoparticles; neurodegenerative diseases; drug delivery; central nervous system; neuroprotective drugs; fluorescent labeling; DiI; coumarin 6; rhodamine 123; Cy5.5; quantum yield; brightness; stability of fluorescent label; confocal microscopy; intracellular internalization; in vivo neuroimaging; double-emulsion method; dry powder inhalation; antigen release; porous PLGA particles; microfluidics; methotrexate; chitosan; PLA/PLGA; sustained release; micro-implant; animal model; minimally invasive; drug delivery system; nanoparticles; poly (lactic-co-glycolic acid) (PLGA); microfluidic; pharmacokinetics (PK) and biodistribution; atorvastatin calcium; poly(lactide-co-glycolide); polymeric nanoparticles; carrageenan induced inflammation; anti-inflammatory; radiolabeled nanoparticles; nuclear medicine; photothermal therapy; phthalocyanine; SKOVip-kat; Katushka; TurboFP635; JO-4; PLGA; orthotopic tumors; 3D culture; spheroids; poly(lactic-co-glycolic acid); nanomedicine; scale-up manufacturing; clinical translation; inline sonication; tangential flow filtration; lyophilization; downstream processing; H. pylori; design of experiments; poly(lactic-co-glycolic) acid; size; cancer; chemoimmunotherapy; immunogenic cell death; immune checkpoint blockade; PNA5 glycopeptide; mas receptor; angiotensin; PLGA diblock copolymer; ester and acid-end capped; double emulsion solvent evaporation; biocompatible; biodegradable; cardiovascular; nanoparticle; solid-state characterization; in vitro; drug release kinetics modeling; PEGylation; amine; emulsion; polyvinyl alcohol (PVA); Pluronic triblock copolymer; trehalose; sucrose; Indomethacin; solvents; stabilizers; morphology; particle-size; encapsulation; drug release; cytotoxicity