TABLE 5.
Nanoformulation-based natural products for the treatment of psoriasis.
Nanoformulation | Category | Drug | Drug limitations | Preparation method | Therapy | Remark | References |
---|---|---|---|---|---|---|---|
Liposomes | Alkaloids | Capsaicin | Irritating, burning effects on the skin | The thin-film hydration method | Topical application | Reduced the side effects of the drug and increased the therapeutic efficacy | Gupta et al. (2016) |
Ethosomes | Phenylpropanoids | Psoralen | Poor permeability | The injection ultrasonic combination method | Topical application | Enhanced cutaneous absorption of drugs and permeability | Zhang et al. (2014b) |
Niosomes | Phenylpropanoids | 8-Methoxypsoralen | Gastrointestinal adverse effects and a higher risk of severe complications | The thin film hydration method | Psoralen ultraviolet a (PUVA) therapy | Promoted penetration and accumulation of 8-Methoxypsoralen | Kassem et al. (2017) |
NLCs | Alkaloids | Pentoxifylline | Poor permeability | The thin lipid film-based microwave-assisted rapid technique | Topical application | Enhanced anti-inflammatory potential | Ghate et al. (2019) |
Phenylpropanoids | Curcumin | Highly hydrophobic molecule with low water solubility | The hot emulsification method | Topical application | Improved permeation and skin retention, showed no toxicity toward keratinocyte cells | Rapalli et al. (2020) | |
Terpenoids | Thymol | High volatility and can also decompose due to heat, humidity, oxygen, or light | The sonication method | Topical application | Enhanced anti-inflammatory potential | Pivetta et al. (2018) | |
Terpenoids | Tripterine | Long-term oral administration of TRI can lead to toxicity on renal and reproductive systems | The emulsification evaporation method | Topical application | Revealed the sustained release characteristics, showed great stability and biocompatibility | Kang et al. (2019) | |
Nanoemulsions | Terpenoids | Paclitaxel | Poor solubility and permeability | Low energy emulsification methods | Dermal/Oral delivery | Enhanced absolute and per oral bioavailability | — |
Phenylpropanoids | 8-Methoxypsoralen | Poor permeability | High-energy method | Topical application | Enhanced retention in viable skin | Oliveira et al. (2018) | |
Organic acids | Salicylic acid | Poor aqueous solubility and instability | Low-energy, spontaneous emulsification method | Topical application | Improved anti-inflammatory action | Khandavilli and Panchagnula. (2007) | |
Dendrimers | Phenylpropanoids | 8-Methoxypsoralene | Gastrointestinal side effects and complications | The divergent method | Topical application | Enhanced skin permeation and concentration of 8-Methoxypsoralen in epidermis and dermis | Borowska et al. (2012) |