Frontiers in Bioengineering and Biotechnology, 2023 · DOI: 10.3389/fbioe.2023.1261288 · Published: August 16, 2023
Spinal cord injuries are difficult to treat due to the blood-spinal cord barrier, drug targeting issues, and complex injury site conditions. Lipid nanovesicles, both cell-derived and synthetic, show promise as biocompatible delivery systems that can penetrate the barrier and target the injury site. Lipid nanovesicles are engineerable, have low immunogenicity and toxicity, making them promising for future spinal cord injury treatments, although most research is in preclinical stages. Researchers are exploring lipid nanovesicles for targeted drug delivery to the spinal cord, addressing challenges such as crossing the blood-spinal cord barrier and delivering drugs to specific injury sites at the right concentration and duration.
Lipid nanovesicles can improve the efficiency of drug delivery to the spinal cord, reducing side effects and increasing bioavailability.
Lipid nanovesicles can be used to deliver multiple drugs to achieve a combined therapeutic effect, targeting different pathological processes in SCI.
Lipid nanovesicles can be tailored to target specific cell types and tissues in the spinal cord, allowing for more personalized treatment strategies.