Pulmonary drug delivery strategies: A concise, systematic review - Wikidata - awgldk - TriplyDB

Pulmonary drug delivery strategies: A concise, systematic review

Pulmonary drug delivery strategies: A concise, systematic review

http://www.wikidata.org/entity/Q35746468

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Preparation, characterization, and potential application of chitosan, chitosan derivatives, and chitosan metal nanoparticles in pharmaceutical drug delivery siRNA delivery to the lung: what's new?A novel approach for lung delivery of rifampicin-loaded liposomes in dry powder form for the treatment of tuberculosis.Design and Biological Evaluation of Delivery Systems Containing Bisphosphonates Targeting the pro-inflammatory factor CCL2 (MCP-1) with Bindarit for influenza A (H7N9) treatment.Study of Lysozyme-Loaded Poly-L-Lactide (PLLA) Porous Microparticles in a Compressed CO₂ Antisolvent Process.Supercritical CO₂-Assisted Spray Drying of Strawberry-Like Gold-Coated Magnetite Nanocomposites in Chitosan Powders for Inhalation.The lungs and drug delivery.Tracheobronchial nebulizer DIVO™.The advantages of pulmonary delivery of therapeutic siRNA.In vitro/in vivo evaluation of agar nanospheres for pulmonary delivery of bupropion HCl.Proof-of-Principle Study in a Murine Lung Infection Model of Antipseudomonal Activity of Phage PEV20 in a Dry-Powder Formulation.Exosome-Mediated Small RNA Delivery: A Novel Therapeutic Approach for Inflammatory Lung Responses

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Pulmonary drug delivery strategies: A concise, systematic review

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Pulmonary drug delivery strategies: A concise, systematic review

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J S Patil

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S Sarasija

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Deagglomeration of dry powder pharmaceutical aerosols.

Effect of design on the performance of a dry powder inhaler using computational fluid dynamics. Part 1: Grid structure and mouthpiece length.

Localization of the peptide transporter PEPT2 in the lung: implications for pulmonary oligopeptide uptake.

Distribution and function of the peptide transporter PEPT2 in normal and cystic fibrosis human lung.

Production of solid lipid nanoparticle suspensions using supercritical fluid extraction of emulsions (SFEE) for pulmonary delivery using the AERx system.

Biopharmaceutical powders: particle formation and formulation considerations.

Immunological and toxicological implications of short-term studies in animals of pharmaceutical aerosol delivery to the lungs: relevance to humans.

Solution-based particle formation of pharmaceutical powders by supercritical or compressed fluid CO2 and cryogenic spray-freezing technologies.

The rationale for aerosolized antibiotics.

Receptors for unopsonized particles: the role of alveolar macrophage scavenger receptors.

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44-49

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