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. 2022 Feb 13;17(2):153–176. doi: 10.1016/j.ajps.2022.02.001

Table 1.

Pros and cons of the viral and non-viral delivery carrier used for CRISPR/Cas9 delivery to the eye.

Delivery vehicle Pros Cons
Viral vectors (Lentivirus, Adenovirus, baculovirus)
  • High transfection ex vivo

  • High efficiency

  • Risk of insertion mutagenesis [13]

  • Immune response [13]

  • Low loading efficiency

  • Low in vivo efficiency

  • Difficult to handle

  • High cost

  • Cannot deliver RNPs

Non-Viral vectors
(Polymeric nanoparticles, dendrimers, exosomes, Liposomes, Lipid nanoparticle, polymeric micelles)
  • Low cost

  • Ease of handling and

  • Ease of preparation

  • High loading

  • Can be prepared for target delivery

  • Low immunogenicity

  • Can deliver RNPs

  • In vivo stability

  • Less risk of mutagenesis

  • Flexibility

  • Comparative low efficiency and transfection

  • Toxicity

  • Scalability