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. Author manuscript; available in PMC: 2020 Sep 1.
Published in final edited form as: Adv Healthc Mater. 2019 Aug 12;8(18):e1900506. doi: 10.1002/adhm.201900506

Table 2.

Comparing the characteristics of four soft nanoparticles: nanoliposomes, dendrimers, polymeric micelles, and nanogels. Images reproduced with permission.[126,127]

Type Nanoliposomes
graphic file with name nihms-1046316-t0005.jpg
Dendrimers
graphic file with name nihms-1046316-t0006.jpg
Polymeric Micelles
graphic file with name nihms-1046316-t0007.jpg
Nanogels
graphic file with name nihms-1046316-t0008.jpg
Nature • Natural • Synthetic • Synthetic • Natural
• Synthetic
Size • ~50 nm • 2–15 nm • 10–100 nm • <100 nm
Preparation methods • Microfluidization
• Extrusion
• Sonication
• Convergent
• Divergent
• Direct dissolution
• Film casting
• Dialysis
• Oil in water emulsion
• Physical self-assembly of interactive polymers
• Chemical synthesis in colloidal environments
• Chemical crosslinking of preformed polymers
• Template-assisted nanofabrication
Adv. • Biocompatible
• Biodegradable
• Non-toxic
• Non-immunogenic
• Controlled and targeted drug delivery
• Sustained release
• Increase drug efficacy and stability
• Many administration routes
• Biodegradable
• Very small size
• Well-defined and flexible structure
• Precise controllability
• High deformability
• Stimuli-responsiveness
• Surface functionality
• Small size
• Narrow distribution
• Easy sterilization
• High structural stability
• Low toxicity
• Excellent blood stability
• High water solubility
• Controlled release functions
• Biocompatible
• Large surface area
• Stimuli sensitivity
• High water content/swellability and hydrophilicity
• Tunable nanoparticle size
• Site targeting
• Controllable release
• Increased drug stability
Disadv. • Low solubility
• Short half-life
• High production cost
• Difficult sterilization
• Lysosomal degradation
• Low efficacy active targeting
• Low biocompatibility
• Significant liver accumulation
• Material’s homogeneity deterioration
• Great batch-to-batch variability
• Low biocompatibility
• Difficult synthesis
• Difficult to scale-up
• Limited choice of monomers
• Concerns over nanotoxicity and storage stability
• Challenging optimization of degradation mechanism, biodistribution, and component toxicity
• Drug instability and rapid degradation in the bloodstream
REF. [92,96,128] [101,129] [128,130132] [114,127,133]