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Advancements in Gene Therapy Delivery Methods
Exploring the utilization of chimeric viruses, adeno-associated viruses, and lipid nanoparticles in gene therapy delivery, and the considerations between ex vivo and in vivo approaches based on payload size and target cell characteristics. The chapter highlights transformational technologies in treating patients, advancing viral vectors' efficiency, and improving manufacturing processes to make gene therapy treatments more accessible for a wider range of diseases beyond severe and lethal conditions.