2019
DOI: 10.1016/j.ejps.2019.104968
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Cytotoxicity screening of emulsifiers for pulmonary application of lipid nanoparticles

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Cited by 13 publications
(7 citation statements)
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“…Poloxamers are amphiphatic polymers of polyoxypropylene and polyoxyethylene that were shown to increase the diffusion rate of coated SLNs across artificial sputum media in vitro compared with uncoated SLNs [ 149 ]. Another study confirmed that poloxamer showed no cytotoxicity in cultured human alveolar epithelial cells, making it suitable for pulmonary applications [ 150 ]. A team in 2020 demonstrated that short bacteriophage heptapeptides screened from a phage display library also had the ability to improve particle transport across ex vivo CF mucus [ 148 ].…”
Section: Challenges Of Inhaled Lnp Therapeutics and Design Considerat...mentioning
confidence: 99%
See 1 more Smart Citation
“…Poloxamers are amphiphatic polymers of polyoxypropylene and polyoxyethylene that were shown to increase the diffusion rate of coated SLNs across artificial sputum media in vitro compared with uncoated SLNs [ 149 ]. Another study confirmed that poloxamer showed no cytotoxicity in cultured human alveolar epithelial cells, making it suitable for pulmonary applications [ 150 ]. A team in 2020 demonstrated that short bacteriophage heptapeptides screened from a phage display library also had the ability to improve particle transport across ex vivo CF mucus [ 148 ].…”
Section: Challenges Of Inhaled Lnp Therapeutics and Design Considerat...mentioning
confidence: 99%
“…Additionally, toxicology tests aimed at the pulmonary administration route need to cover particle morphology, size distribution, surface chemistry and agglomeration tendency, which goes beyond classical toxicology tests focused on drug dose and composition [ 26 ]. Steiner et al recently incorporated three orally-approved excipients: Kolliphor RH40Poloxamer 188 and Tween 80, into drug-loaded SLNs in vitro [ 150 ]. These particles demonstrated low toxicity and suitability for pulmonary applications in cultured human alveolar epithelial cells and macrophages [ 150 ].…”
Section: Challenges Of Inhaled Lnp Therapeutics and Design Considerat...mentioning
confidence: 99%
“…Thus, human cells tend to be better appropriate for screening adverse effects in the human lungs. 293 As cellulose nanocrystals (CNCs) expand in the generation, promoting healthy employment practices will be crucial to distance control and development. Particles other than CNCs with comparable high aspect ratios demonstrated inhalation toxicity.…”
Section: Toxicity Of Inhaled Nanoparticlesmentioning
confidence: 99%
“…Due to the specific advantages, i.e., lower proliferation rate, more extensive cell size, human cells displayed lower cytotoxicity than murine cells. Thus, human cells tend to be better appropriate for screening adverse effects in the human lungs . As cellulose nanocrystals (CNCs) expand in the generation, promoting healthy employment practices will be crucial to distance control and development.…”
Section: Toxicity Of Inhaled Nanoparticlesmentioning
confidence: 99%
“…Most of the studies about the pulmonary route of administration have used aerosol formulations that have been very effective for the treatment of respiratory inflammation and other lung disorders [65]. This pathway represents a possibility for systemic and non-invasive release of proteases [66]. Another therapeutic route is the transdermal one, which uses adhesives and is a painless alternative to injections.…”
Section: Formulation Of Proteasesmentioning
confidence: 99%