Skip to main content
. 2021 Sep 22;11(10):2467. doi: 10.3390/nano11102467

Table 1.

Summary of advantages and disadvantages of various systems used for co-delivery of small molecule drugs and siRNA.

Delivery System Advantages Disadvantages
Mesoporous Silica Nanoparticles
  • Naturally abundant

  • Modifiable, nano-sized mesoporous structure

  • Large pore volume

  • High specific surface area

  • Dual-functional exterior and interior surfaces

  • Good biocompatibility and biodegradability

  • Can be incorporated in magnetic applications

  • Protects guest molecules before reaching target site

  • Extra modifications or coatings on surface for specific functions (targeted delivery, co-delivery of drugs and siRNA, sustained release of drug, etc.)

  • Unsuitable for encapsulating drug molecules larger than the size of its pores

  • Extra coating needed to enhance stability of drug in the carrier

Polymeric Materials
  • Cationic polymer encourages attachment of siRNA

  • Hydrophobic core eases encapsulation

  • Can be modified to have controlled release behaviours

  • Can be designed to be sensitive to pH, temperature, chemical substances and enzymes

  • Preferential accumulation in tumour tissues

  • Various co-polymer combinations can be done to explore various potentials

  • Protects guest molecules before reaching target site

  • Toxicity dependent on the chemical structure of polymers

  • Appropriate design of polymer drug carrier is vital

  • Modifications are needed for better performance

  • Structure modification is required in certain conditions to reduce the cytotoxicity

Liposomes
  • Enables encapsulation of active agents

  • Shielding effect reduces toxicity of chemotherapy drugs

  • Improves cellular uptake

  • Protects guest molecules before reaching target site

  • Confers good drug stability

  • Good controlled release profile

  • Can be modified into cationic liposome for siRNA conjugation

  • Manipulatable size

  • Smart liposomes (sensitive to pH, temperature, enzymes and magnetic field)

  • Imaging agents can be attached

  • Good biocompatibility and biodegradability

  • Low immunogenicity

  • Able to penetrate the stratum corneum

  • Restricted by rapid clearance from the bloodstream in the reticuloendothelial system (RES)

  • Modifications are needed to prolong circulation time in blood

  • Ligand attachment is needed for site-specific delivery

  • Appropriate selection is needed depending on the application

Dendrimers
  • Unique and precise molecular structure

  • Conjugation of drugs through various types of bonding

  • Uniform globular structure and molecular weight

  • Wide range of generation number can be chosen for specific applications

  • Manipulatable size and lipophilicity

  • Can be engineered with ligands

  • Low systemic toxicity

  • Protects guest molecules before reaching target site

  • Properties are highly dependent on functional group of outer shell

  • Performance of carrier is dependent on the appropriate functional group chosen

  • Appropriate selection and method of encapsulation is crucial

Gold nanoparticles
  • Various morphologies available for different applications

  • Variable optical properties

  • Suitable for bioimaging applications

  • Passive and preferential accumulation at tumour site

  • High specific surface area

  • Antimicrobial properties

  • Good biocompatibility and biodegradability

  • Least reactive element

  • Ligands can be conjugated for various applications

  • High cost

  • Rare

  • Ligand attachment is needed for site-specific delivery