Table 1.
Examples and respective properties of hydrophobic and hydrophilic polymers as well as amphiphilic block copolymers commonly used in the formulation of polymeric micelles.
Polymers | Properties | References | |
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Hydrophobic Polymers | poly(D,L-lactide)–PLA | PLA-based PMs are clinically-approved (Genexol®, Nanoxel®). | [11,12,13,14,15,17,18] |
poly(lactic-co-glycolic acid)–PLGA | PLGA is used as a biodegradable surgical suture in the clinic (Vicryl®). Biodegradable. |
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poly(β-benzyl-l-aspartate) | The presence of the benzyl group grants increased hydrophobicity. Biodegradable. |
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poly(γ-benzyl-α, l-glutamate) | The presence of the benzyl group grants increased hydrophobicity. Ultra-high loading capacity for various poorly soluble drugs (ex. paclitaxel, etoposide) as well as a versatile library of polymer structures. |
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poly(2-n-butyl-2-oxazoline) | The presence of the benzyl group grants increased hydrophobicity. Ultra-high loading capacity for several poorly soluble drugs, such as curcumin. |
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Hydrophilic Polymers | polyethylene glycol (PEG) | Has been used in clinically-approved nanoformulations including PMs (Genexol® PM). | |
poly(2-methyl-2-oxazoline)–PMeOx | PMeOx is more hydrophilic than PEG. | ||
poly(sarocosine) | Evaluated as PEG replacement. Biodegradable. |
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dextran | Has been used as a component in block and graft copolymers. Has highly variable molecular weight and dextran has been used as an excipient in clinically-approved injectable products (Feraheme®). Biodegradable. |
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Amphiphilic block copolymers | poly(propylene oxide)–PPO poly(ethylene oxide)–PEO PEOn-PPOm-PEOn |
PEOn-PPOm-PEOn triblock copolymers are usually used in pharmaceutical formulations as non-active pharmaceutical ingredients. Pluronic®-based PMs entrapping Doxorubicin, SP1049C, had entered clinical trials and have been granted orphan drug designation by the FDA. Commercially available as poloxamers (Pluronic®). Biocompatible. |