Our human lung lysosomes provide a highly specialized in vitro model for studying lysosomal function, intracellular trafficking, and drug accumulation in pulmonary tissue. Isolated from healthy human lung tissue, these lysosomes are enriched to preserve structural integrity and enzymatic activity, making them ideal for evaluating respiratory drug delivery, lysosome-mediated degradation, and potential pulmonary toxicity.
These lysosomes support a broad range of applications, including subcellular pharmacokinetics, inhaled drug processing, and mechanistic studies of lysosome-related diseases in lung tissue.