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
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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
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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
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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
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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
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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
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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
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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
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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
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