DEVELOPMENT AND EVALUATION OF LIPID–POLYMER HYBRID NANOPARTICLES FOR TARGETED SIRNA DELIVERY IN CANCER THERAPY

Gene therapy is a therapeutic approach that involves the introduction, removal, or modification of genetic material within a patient’s cells to treat or prevent disease. The fundamental principle is to correct or regulate defective genes responsible for disease pathogenesis rather than merely treating symptoms. The concept was first formally proposed in the 1970s and later advanced through recombinant DNA technology and molecular biology innovations Gene therapy works by delivering nucleic acids—such as DNA or RNA—into target cells using viral or non-viral vectors. The therapeutic gene must reach the appropriate intracellular compartment (nucleus or cytoplasm) to exert its function. Efficient gene delivery requires overcoming multiple biological barriers, including enzymatic degradation, immune recognition, cellular uptake, and endosomal escape.

Authors

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-07-30
DOI
https://doi.org/10.5281/zenodo.21696771
Primary Topic
RNA Interference and Gene Delivery
Type
article
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article

DEVELOPMENT AND EVALUATION OF LIPID–POLYMER HYBRID NANOPARTICLES FOR TARGETED SIRNA DELIVERY IN CANCER THERAPY

Ms. Komal Digambar Gangurde* Dr. C.D. Patil
Zenodo (CERN European Organization for Nuclear Research)
RNA Interference and Gene Delivery
article

DEVELOPMENT AND EVALUATION OF LIPID–POLYMER HYBRID NANOPARTICLES FOR TARGETED SIRNA DELIVERY IN CANCER THERAPY

Ms. Komal Digambar Gangurde* Dr. C.D. Patil
article en

Abstract

Gene therapy is a therapeutic approach that involves the introduction, removal, or modification of genetic material within a patient’s cells to treat or prevent disease. The fundamental principle is to correct or regulate defective genes responsible for disease pathogenesis rather than merely treating symptoms. The concept was first formally proposed in the 1970s and later advanced through recombinant DNA technology and molecular biology innovations Gene therapy works by delivering nucleic acids—such as DNA or RNA—into target cells using viral or non-viral vectors. The therapeutic gene must reach the appropriate intracellular compartment (nucleus or cytoplasm) to exert its function. Efficient gene delivery requires overcoming multiple biological barriers, including enzymatic degradation, immune recognition, cellular uptake, and endosomal escape.

Zenodo (CERN European Organization for Nuclear Research)
Openalex Percentile: Top 15%
RNA Interference and Gene Delivery
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