A trophic composition with a complex nutritive base and collagenase inhibitor promotes corneal epithelial cell viability.
Acetate buffers at pH 4.5-5.5 prevent aggregation of TACI-immunoglobulin fusion proteins during storage.
Aceclidine eye drops activate M1 receptors to constrict the pupil, improving near vision without ciliary muscle spasms.
Novel pyrazolo[3,4-b]pyridine compounds inhibit xanthine oxidase to reduce severe side effects from allopurinol.
Imatinib eye drops inhibit tyrosine kinase activity to prevent corneal damage and inflammation in dry eye syndrome.
Exosomes from mesenchymal stem cells deliver HSP70 protein to shield auditory hair cells from ototoxic drug damage.
Phase-separated multi-block copolymers prevent protein aggregation and acidic micro-environments by creating hydrophilic pathways for sustained release.
Pyridopyrazinone derivatives restore glucose-responsive insulin release, preventing hyperinsulinemia and beta cell exhaustion in type 2 diabetes treatment.
A dynamic dosing regimen using VEGF antagonists adjusts treatment intervals to maintain therapeutic efficacy.
Topical amarogentin activates bitter taste receptors to reduce inflammation and strengthen skin barrier function.
Guide RNA targets single nucleotide polymorphism in mutant allele to enable precise CRISPR-mediated mRNA degradation.
Peptide-based proteasome inhibitors with C-terminal electrophilic groups inactivate target enzymes via covalent bonding.
Formula I compounds bypass reduced nitric oxide bioavailability by directly activating heme-dependent soluble guanylate cyclase to treat pulmonary hypertension.
Selective Bcl-2 inhibitors minimize off-target effects on Bcl-xL while treating systemic lupus erythematosus, lupus nephritis, and Sjogren's Syndrome.