Peptide gels that act like depots
Peptide drugs fail for a boring reason: delivery. Self-assembling peptide hydrogels try to fix that by turning peptides into local depots that hold and release medicine over time.
Tag
Peptides often fail for a boring reason: delivery. This tag tracks delivery ideas like depots, conjugates, and designs that change where a peptide goes and how long it lasts.
Peptide drugs fail for a boring reason: delivery. Self-assembling peptide hydrogels try to fix that by turning peptides into local depots that hold and release medicine over time.
A new PNAS study gives cell-penetrating peptides a more physical explanation: they may cross membranes by opening submillisecond pores, turning one of drug delivery's strangest tricks into something medicine can start to measure.
New work on antimicrobial peptides points to a less glamorous but more decisive challenge: many peptides can punch holes in microbes, but the future belongs to systems that can predict, package, or localize that violence before it reaches human cells.
A cluster of new preclinical peptide-drug conjugate studies points to a subtle shift in oncology: using familiar cancer receptors less as signaling switches and more as delivery portals for toxic payloads.
A preclinical teriparatide delivery study shows why the next long-acting peptide problem may be timing: some medicines work because the body sees pulses, not a constant drip.
Researchers describe an enveloped virus-mimicking particle built from a simplified peptide plus tuned lipids, aiming for repeatable mRNA delivery to extrahepatic tissues like lung and spleen.
A new mouse study tests an exosome-based ‘biomimetic’ delivery idea for oral octreotide, hinting at a path beyond permeability enhancers but leaving big manufacturing and translation questions.
Researchers describe AMG 133, an antibody-peptide conjugate designed to combine GIP receptor antagonism with GLP-1 receptor agonism. It’s a design story about longer-acting multi-target biology, not a new approved therapy.
A mouse study reports an enzyme-responsive peptide that forms a bladder-local hydrogel depot to retain BCG longer, aiming to reduce washout and improve immune activation in non-muscle-invasive bladder cancer.
A 2026 Advanced Science paper introduces INB3P, a machine-learning framework built for small peptide datasets. It predicts blood-brain barrier-penetrating motifs and offers interpretability tools, but still needs prospective validation.
Researchers report benzaldehyde-tagged cell-penetrating peptides can anchor to membrane proteins via reversible imine chemistry, helping cargo escape endosomes and reach the cytosol.