Results 151 to 160 of about 371,071 (337)
Antimicrobial peptide (AMP)‐loaded nanocarriers provide a multifunctional strategy to combat drug‐resistant Mycobacterium tuberculosis. By enhancing intracellular delivery, bypassing efflux pumps, and disrupting bacterial membranes, this platform restores phagolysosome fusion and macrophage function.
Christian S. Carnero Canales +11 more
wiley +1 more source
Li Y, Hao L, Liu F, et al. Int J Nanomedicine. 2019;14:5875–5894.The authors have advised that affiliation 1 for this paper was presented incorrectly as it was split into two affiliations and this was not corrected before the paper was published ...
Li Y +12 more
doaj
The Cell-Penetrating Peptide Tat Facilitates Effective Internalization of PSD-95 Inhibitors Into Blood–Brain Barrier Endothelial Cells but less Efficient Permeation Across the Blood–Brain Barrier In Vitro and In Vivo [PDF]
Emma Lisa Al Humaidan +11 more
openalex +1 more source
Stromal vascular fraction (SVF) may enhance nerve repair, especially when delivered in a self‐assembling peptide hydrogel (SAPH). In vitro, softer SAPH increased neuronal explant outgrowth and supported greater SVF viability and proliferation. In a rat sciatic defect, SVF in an optimized SAPH produced motor and sensory recovery equivalent to autograft ...
Liam A. McMorrow +6 more
wiley +1 more source
Hybrid Scaffolds Decouple Biochemical & Biophysical Regulation of Cell Phenotype
Replicating tissue‐specific extracellular matrix is crucial for understanding its role in disease. This work demonstrates independent control over stiffness, composition and 3D collagen architecture using hybrid scaffolds: patterned collagen perfused with defined hydrogels.
Xinyuan Song +17 more
wiley +1 more source
Cell-Penetrating Peptides for Antiviral Drug Development [PDF]
Melaine Delcroix, Lee W. Riley
openalex +1 more source
Peptomer Linkers Enable Kinetic Control over Co‐Delivery of Multiple Chemotherapeutics
A key challenge in combinatorial chemotherapeutic drug delivery is independent control over release kinetics, especially with drugs of similar size and structure. Here, peptoid substitutions to proteolytically degradable peptides enabled the design of fast and slow‐releasing drug linkers.
Carolyn M. Watkins +3 more
wiley +1 more source
Comparison of Cationic and Amphipathic Cell Penetrating Peptides for siRNA Delivery and Efficacy
Robert H. Mo +2 more
openalex +2 more sources

