
Expert Review of Respiratory Medicine, Journal Year: 2024, Volume and Issue: unknown, P. 1 - 3
Published: Nov. 27, 2024
Language: Английский
Expert Review of Respiratory Medicine, Journal Year: 2024, Volume and Issue: unknown, P. 1 - 3
Published: Nov. 27, 2024
Language: Английский
Pharmaceutics, Journal Year: 2024, Volume and Issue: 16(5), P. 680 - 680
Published: May 17, 2024
Lung diseases have received great attention in the past years because they contribute approximately one-third of total global mortality. Pulmonary drug delivery is regarded as one most appealing routes to treat lung diseases. It addresses numerous drawbacks linked traditional dosage forms. presents notable features, such as, for example, a non-invasive route, localized delivery, low enzymatic activity, degradation, higher patient compliance, and avoiding first-pass metabolism. Therefore, pulmonary route commonly explored delivering drugs both locally systemically. Inhalable nanocarrier powders, especially, lipid nanoparticle formulations, including solid-lipid nanostructured-lipid nanocarriers, are attracting considerable interest addressing respiratory thanks their significant advantages, deep deposition, biocompatibility, biodegradability, mucoadhesion, controlled released. Spray drying scalable, fast, commercially viable technique produce nanolipid powders. This review highlights ideal criteria inhalable spray-dried SLN NLC powders administration route. Additionally, promising inhalation devices, known dry powder inhalers (DPIs) powder-based medications, applications treating chronic conditions, considered.
Language: Английский
Citations
7International Journal of Pharmaceutics, Journal Year: 2024, Volume and Issue: 657, P. 124182 - 124182
Published: April 30, 2024
Language: Английский
Citations
5Pharmaceutics, Journal Year: 2024, Volume and Issue: 16(8), P. 969 - 969
Published: July 23, 2024
Lung cancer is the leading cause of cancer-related mortality worldwide, largely due to limited efficacy anticancer drugs, which primarily attributed insufficient doses reaching lungs. Additionally, patients undergoing treatment experience severe systemic adverse effects distribution drugs non-targeted sites. In light these challenges, there has been a growing interest in pulmonary administration for lung cancer. This route allows be delivered directly lungs, resulting high local concentrations that can enhance antitumor while mitigating toxic effects. However, poses challenge overcoming mechanical, chemical, and immunological defenses respiratory tract prevent inhaled drug from properly penetrating To overcome drawbacks, use nanoparticles inhaler formulations may promising strategy. Nanoparticles assist minimizing clearance, increasing penetration into epithelium, enhancing cellular uptake. They also facilitate increased stability, promote controlled release, delivery target sites, such as tumor environment. Among them, chitosan-based demonstrate advantages over other polymeric nanocarriers their unique biological properties, including activity mucoadhesive capacity. These properties have potential when administered via route. view above, this paper provides an overview research conducted on drug-loaded incorporated devices Furthermore, article addresses emerging technologies, siRNA (small interfering RNA), context therapy. Particularly, recent studies employing are described.
Language: Английский
Citations
5Carbohydrate Polymers, Journal Year: 2024, Volume and Issue: 345, P. 122571 - 122571
Published: Aug. 5, 2024
Language: Английский
Citations
5Emergent Materials, Journal Year: 2024, Volume and Issue: unknown
Published: April 24, 2024
Language: Английский
Citations
4ACS Nano, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 18, 2025
Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS), a rapidly progressing failure condition, results in high mortality rate, especially severe cases. Numerous trials have investigated various pharmacotherapy approaches, but their effectiveness remains uncertain. Here, we present an inhaled nanoformulation of fingolimod (FTY720)-nobiletin (NOB)- poly(lactic-co-glycolic) acid (PLGA) nanoparticles (NPs) with good biocompatibility and sustained-release pharmacological effect. The formulation decreases the toxicity FTY720 increases bioavailability NOB since use PLGA to encapsulate at same time. In vitro, comparison treatment pure drug, demonstrated that FTY720-NOB-PLGA NPs can reduce interleukin-6 (IL-6) reactive oxygen species (ROS) release by macrophages after lipopolysaccharide (LPS) stimulation more efficiently. vivo, used inhalation tower system allowed exposure unanesthetized mice aerosolized under controlled conditions. We attenuate LPS suppressing cytokine release, such as IL-6 tumor necrosis factor-α (TNF-α). trigger pathway ALI, including nuclear factor κ-light-chain-enhancer activated B cells (NF-κB) p38 mitogen-activated protein kinase, was also efficiently inhibited. Furthermore, provided safety profile, without detrimental effects on biochemical markers function. feasibility administering noninvasively continuous monitoring developed show excellent promise for acute therapy future.
Language: Английский
Citations
0Materials Today Bio, Journal Year: 2025, Volume and Issue: 31, P. 101616 - 101616
Published: Feb. 26, 2025
Language: Английский
Citations
0International Journal of Pharmaceutics, Journal Year: 2025, Volume and Issue: unknown, P. 125509 - 125509
Published: March 1, 2025
Language: Английский
Citations
0Synthesis lectures on biomedical engineering, Journal Year: 2025, Volume and Issue: unknown, P. 63 - 112
Published: Jan. 1, 2025
Language: Английский
Citations
0AAPS PharmSciTech, Journal Year: 2024, Volume and Issue: 25(6)
Published: Aug. 2, 2024
Language: Английский
Citations
3