2014
DOI: 10.3109/10717544.2013.879354
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Development of a drug delivery system for the inner ear using poly(amino acid)-based nanoparticles

Abstract: (2015) Development of a drug delivery system for the inner ear using poly(amino acid)-based nanoparticles, Drug Delivery, 22:3, 367-374, DOI: 10.3109/10717544.2013 Objective: To evaluate the permeability and safety of a drug delivery system for the inner ear using a poly(2-hydroxyethyl aspartamide) (PHEA) polymersome. Materials and methods: One-month-old male C57/BL6 mice were used. We administered the same amount of the fluorescent dye, Nile red, into the middle ear in two forms: loaded in PHEA polymersomes… Show more

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Cited by 19 publications
(9 citation statements)
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“…27 In addition, this reaction is widely used for conjugation of cysteinecontaining peptides and proteins. 28,29 In contrast, the binding of small peptides (such as A666 peptide, which is isolated from 3 rounds of sequential phage display peptide libraries) to their receptors is highly specific with high affinity, and they are generally considered less immunogenic than IgG antibodies. 26 One of the main issues investigated in this study was whether A666-NP can penetrate the RWM and accumulate to OHCs.…”
Section: Discussionmentioning
confidence: 99%
“…27 In addition, this reaction is widely used for conjugation of cysteinecontaining peptides and proteins. 28,29 In contrast, the binding of small peptides (such as A666 peptide, which is isolated from 3 rounds of sequential phage display peptide libraries) to their receptors is highly specific with high affinity, and they are generally considered less immunogenic than IgG antibodies. 26 One of the main issues investigated in this study was whether A666-NP can penetrate the RWM and accumulate to OHCs.…”
Section: Discussionmentioning
confidence: 99%
“…686 Safety 687 Nanoparticulate systems tested in animals following a single intratympanic administration 688 showed a good safety profile. They did not exhibit negative effects on the hearing 689 functionand did not provoke any hair cell loss or histological damages (Scheper et al, 2009, 690 Zhang et al, 2011, Kim et al, 2014or inflammation (Zou et al, 2014). 691 However, SPIONs exhibited a neurotoxic effect by disturbing the electrical activity even at 692 low particle concentrations (Gramowski et al, 2010, Pritz et al, 2013.…”
Section: Drug Releasementioning
confidence: 95%
“…formed by the self-assembly of amphiphilic block copolymers such as 601 poly(ethyleneglycol)-b-poly(Ɛ-caprolactone)(PEG-b-PCL)(Roy et al, 2012)or poly(2-602 hydroxyethyl aspartamide (PHEA)(Kim et al, 2014)in an aqueous solution.They have a 603 hydrophobic membrane surrounding an aqueous core and a hydrophilic corona.Their 604 biomimetic structure enables a good tolerance regarding the immune system. Hydrophilic 605 drugs are loaded in the core and hydrophobic ones in the membrane.606 Dendrimer-based nanoparticles 607 Dendrimers are randomly branched dendritic polymers consisting in the repetition of a 608 unique molecule.…”
mentioning
confidence: 99%
“…Dye encapsulated PHEA showed significant uptake in the organ of Corti, with dye accumulating in inner hair cells. PHEA nanoparticles may be advantageous for the delivery of therapeutics to the inner hair cells (Kim et al, 2015). While there is no known ligand on PHEA nanoparticles to target inner hair cells, preferential accumulation in inner hair cells may be attributed to their physical and chemical properties such as the surface charge and hydrophilicity of the particles and how they bind to the surface of inner hair cells before endocytosis of the nanoparticles.…”
Section: Biomaterials For Local Drug Deliverymentioning
confidence: 99%