Gene Therapy Delivery Systems: Evaluating the Latest Methods for Effective Gene Therapy Delivery

Authors

  • DILEEP KUMAR GARNIPUDI Author
  • Kavitha Parthasarathy Author
  • Samson Israel.D Author
  • Aroun Prasath Author

DOI:

https://doi.org/10.53555/AJBR.v27i4S.3151

Keywords:

CRISPR-Cas9 , hematological , Adenoviral , endocytosis, encapsulated

Abstract

Gene therapy has emerged as a promising approach for treating genetic disorders, cancers, and various diseases. However, effective delivery of therapeutic genes to target cells remains a significant challenge. This review discusses the latest methods in gene therapy delivery systems, evaluating their mechanisms, efficiency, and clinical applications. We categorize these systems into viral and non-viral vectors, highlighting recent advancements, challenges, and future directions.

Author Biographies

  • DILEEP KUMAR GARNIPUDI

    Assistant Professor, Rai university, Ahmedabad & Research scholar, Mohan Babu university, Tirupati, India

  • Kavitha Parthasarathy

    Assistant Professor, Fatima College of Health Sciences, Abu Dhabi, UAE.

     

  • Samson Israel.D

    Professor, St. Ann’s college of Pharmacy, Chirala, Andhra Pradesh, India.

  • Aroun Prasath

    Assistant Professor, Komar University of Science and Technology, Sulaymaniyah, Iraq.

     

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Published

2024-11-11

Issue

Vol. 27 No. 4S (2024): November Issue

Section

Research Article

License

Copyright (c) 2024 African Journal of Biomedical Research

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

How to Cite

Gene Therapy Delivery Systems: Evaluating the Latest Methods for Effective Gene Therapy Delivery. (2024). African Journal of Biomedical Research, 27(4S), 501-509. https://doi.org/10.53555/AJBR.v27i4S.3151