In Situ-Crosslinked Zippersomes Enhance Cardiac Repair by Increasing Accumulation and Retention.
Natalie E JasiewiczKuo-Ching MeiHannah M OhEmily E BonacquistiAmeya ChaudhariCamryn ByrumBrian C JensenJuliane NguyenPublished in: bioRxiv : the preprint server for biology (2024)
Therapeutic delivery to the heart remains inefficient and poses a bottleneck in modern drug delivery. Surgical application and intramyocardial injection of therapeutics carry high risks for most heart attack patients. To address these limitations, we have developed a non-invasive strategy for efficient cardiac accumulation of therapeutics using in situ crosslinking. Our approach achieves high cardiac deposition of therapeutics without invasive intramyocardial injections. Patients admitted with myocardial infarction typically receive intravenous access, which would allow painless administration of Zippersomes alongside standard of care.
Keyphrases
- left ventricular
- drug delivery
- heart failure
- small molecule
- end stage renal disease
- ejection fraction
- newly diagnosed
- healthcare
- palliative care
- atrial fibrillation
- prognostic factors
- low dose
- cancer therapy
- patient reported outcomes
- quality improvement
- chronic pain
- hyaluronic acid
- climate change
- drug release
- health insurance