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Nanoparticle type | Drug | Skin type | Study | Delivery type and penetration | Targeted cutaneous disease pathology | Literature studies |
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Solid lipid nanoparticle | Glucocorticoids, corticosteroids | Human | In vitro and in vivo | Transepidermal delivery, no penetration to the dermis | Inflammatory skin diseases, dermatitis, rheumatic disease | Sivaramakrishnan et al., 2004 [24]; Jensen et al., 2010 [25]; Zhang and Smith, 2011 [26]; Schlupp et al., 2011 [27]; Puglia et al., 2006 [28] |
Solid lipid nanoparticle | Nonsteroidal anti-inflammatory drugs | Human | In vitro and in vivo | Delivery via NP enriched hydrogels with sustained continued drug release to the dermis | Musculoskeletal disorders | Jain et al., 2005 [29]; Bhaskar et al., 2009 [30] |
Solid lipid nanoparticle | Antiandrogens, retinoids | Human | In vitro and in vivo | Transappendageal NP delivery to hair follicle and upper papillary dermis | Skin acne | Munster et al., 2005 [31]; Štecová et al., 2007 [32]; Castro et al., 2007 [33]
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Solid lipid nanoparticle | Antifungal agents | Human | Ex vivo and in vivo | Topical gel delivery of NP with penetration to upper papillary dermis | Skin mycoses | Bhalekar et al., 2009 [34]; Sanna et al., 2007 [35] |
Solid lipid nanoparticle | Retinoids, furocoumarins | Mouse and human | In vivo | Topical gel delivery to the epidermis | Psoriasis | Fang et al., 2008 [19]; Agrawal et al., 2010 [15];
Lin et al., 2010 [36]
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Solid lipid nanoparticle | Tacrolimus | Porcine | In vitro and in vivo | Topical gel delivery with dermal penetration | Atopic dermatitis | Pople and Singh, 2010 [37] |
Nanostructured lipid carriers | Antihypersensitive drugs and anaesthetics | Mouse and human | In vitro and in vivo | Topical gel delivery to the epidermis | Hair loss treatment and pain relief after surgery | Silva et al., 2009 [38]; Puglia et al., 2011 [39] |
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