Search results for "Cell-penetrating peptide"

showing 5 items of 5 documents

Mucus and Cell-Penetrating Nanoparticles Embedded in Nano-into-Micro Formulations for Pulmonary Delivery of Ivacaftor in Patients with Cystic Fibrosis

2017

Here, mucus-penetrating nanoparticles (NPs) for pulmonary administration of ivacaftor in patients with cystic fibrosis (CF) were produced with the dual aim of enhancing ivacaftor delivery to the airway epithelial cells, by rapid diffusion through the mucus barrier, and at the same time, promoting ivacaftor lung cellular uptake. Pegylated and Tat-decorated fluorescent nanoparticles (FNPs) were produced by nanoprecipitation, starting from two synthetic copolymers, and showed nanometric sizes (∼70 nm), a slightly negative ζ potential, and high cytocompatibility toward human bronchial epithelium cells. After having showed the significant presence of poly(ethylene glycol) chains and Tat protein …

Materials scienceCystic FibrosisNanoparticle02 engineering and technologyQuinolones010402 general chemistryAminophenols01 natural sciencesCystic fibrosisIvacaftorchemistry.chemical_compoundmedicineHumansGeneral Materials ScienceMicroparticleDrug CarriersLungαβ-poly-(N-2-hydroxyethyl)-dl-aspartamide (PHEA)ivacaftor (VX-770)mucus-penetrating nanoparticlerespiratory system021001 nanoscience & nanotechnologymedicine.diseaseMucus0104 chemical sciencesMucusnano-into-micro strategymedicine.anatomical_structurechemistrycell penetrating peptideCell-penetrating peptideBiophysicsNanoparticlescystic fibrosis artificial mucus (CF-AM)0210 nano-technologyEthylene glycolmedicine.drug
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Novel cleavable cell-penetrating peptide-drug conjugates: synthesis and characterization

2014

We report the first drug conjugate with a negatively charged amphipathic cell-penetrating peptide. Furthermore, we compare two different doxorubicin cell-penetrating peptide conjugates, which are both unique in their properties, due to their net charge at physiological pH, namely the positively charged octaarginine and the negatively charged proline-rich amphipathic peptide. These conjugates were prepared exploiting a novel heterobifunctional crosslinker to join the N-terminal cysteine residue of the peptides with the aliphatic ketone of doxorubicin. This small linker contains an activated thiol as well as aminooxy functionality, capable of generating a stable oxime bond with the C-13 carbo…

Pharmacologychemistry.chemical_classificationStereochemistryOrganic ChemistryPeptideGeneral MedicineGlutathioneBiochemistryResidue (chemistry)chemistry.chemical_compoundchemistryStructural BiologyDrug DiscoveryDrug deliveryCell-penetrating peptideMolecular MedicineMolecular BiologyLinkerConjugateCysteineJournal of Peptide Science
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Transportan 10 Induces Perturbation and Pores Formation in Giant Plasma Membrane Vesicles Derived from Cancer Liver Cells

2023

Continuous progress has been made in the development of new molecules for therapeutic purposes. This is driven by the need to address several challenges such as molecular instability and biocompatibility, difficulties in crossing the plasma membrane, and the development of host resistance. In this context, cell-penetrating peptides (CPPs) constitute a promising tool for the development of new therapies due to their intrinsic ability to deliver therapeutic molecules to cells and tissues. These short peptides have gained increasing attention for applications in drug delivery as well as for their antimicrobial and anticancer activity but the general rules regulating the events involved in cell…

cell-penetrating peptidesdi-4-ANEPPDHQprotein–membrane interactionsgiant plasma membrane vesiclesprotein–membrane interactions; cell-penetrating peptides; Transportan 10; giant plasma membrane vesicles; phasor approach; Nile Red; di-4-ANEPPDHQ; membrane hydrationTransportan 10Nile RedMolecular BiologyBiochemistryphasor approachSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)membrane hydration
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Common mechanisms underlying membrane modifications induced by protein interactions

2022

di-4-ANEPPDHQa-casein fluorescenceLaurdanRICSprotein-membrane interactionTransportan 10Phasor approachcell-penetrating peptidemembrane hydration
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Increased carrier peptide stability through ph adjustment improves insulin and pth(1-34) delivery in vitro and in vivo rather than by enforced carrie…

2020

Oral delivery of therapeutic peptides is hampered by their large molecular size and labile nature, thus limiting their permeation across the intestinal epithelium. Promising approaches to overcome the latter include co-administration with carrier peptides. In this study, the cell-penetrating peptide penetratin was employed to investigate effects of co-administration with insulin and the pharmacologically active part of parathyroid hormone (PTH(1-34)) at pH 5, 6.5, and 7.4 with respect to complexation, enzymatic stability, and transepithelial permeation of the therapeutic peptide in vitro and in vivo. Complex formation between insulin or PTH(1-34) and penetratin was pH-dependent. Micron-size…

insulinmedicine.medical_treatmentlcsh:RS1-441Pharmaceutical ScienceParathyroid hormonePeptide02 engineering and technologyArticlelcsh:Pharmacy and materia medica03 medical and health sciencespenetratinIn vivoCarrier peptide Cell-penetrating peptide Insulin Intestinal peptide delivery Penetratin PTH(1-34)Membrane activitymedicine030304 developmental biologychemistry.chemical_classification0303 health sciencesLiposomecarrier peptideChemistryInsulinPermeationintestinal peptide delivery021001 nanoscience & nanotechnologyBiophysicsCell-penetrating peptide0210 nano-technologyPTH(1-34)cell-penetrating peptide
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