Solid Lipid Nanoparticles for Topical Drug Delivery: Mechanisms, Dosage Form Perspectives, and Translational Status

被引:40
作者
Liu, Mengyang [1 ]
Wen, Jingyuan [1 ]
Sharma, Manisha [1 ]
机构
[1] Univ Auckland, Fac Med & Hlth Sci, Sch Pharm, POB 1023, Auckland, New Zealand
关键词
Solid lipid nanoparticles; topical delivery; skin penetration; cellular uptake; endocytosis; drug release mechanism; formulation factors; SKIN PENETRATION ENHANCEMENT; IN-VIVO CORRELATION; CARRIERS NLC; TRANSDERMAL DELIVERY; VESICULAR SYSTEMS; DERMAL DELIVERY; CYCLOSPORINE-A; SLN; RELEASE; VITRO;
D O I
10.2174/1381612826666200526145706
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Solid lipid nanoparticles (SLNs) have shown potential as a novel lipid-based drug delivery system the topical applications of innumerable therapeutic compounds. However, the mechanisms governing the absorption and cellular uptake of SLNs through topical route, along with the mechanism of drug release from SLNs still ambiguous, and require further investigation. In addition, the selection of an appropriate dosage form/formulation base is essential for ease of application of SLNs and to enhance dermal and transdermal delivery. Upscaling and regulatory approvals are other challenges that may impede the clinical translation of SLNs. Therefore, this review focusses on different mechanisms involved in skin penetration and cellular uptake of SLNs. This is followed by a comprehensive discussion on the physicochemical properties of SLNs including various formulation and dosage form factors, which might influence the absorption of SLNs through the skin. Finally, translational status with respect to scale-up and regulatory aspects are also discussed. This review will be useful to researchers with an interest in topical applications of SLNs for the efficient delivery of drugs and cosmetics.
引用
收藏
页码:3203 / 3217
页数:15
相关论文
共 159 条
[1]   Development, Optimization, and Evaluation of Carvedilol-Loaded Solid Lipid Nanoparticles for Intranasal Drug Delivery [J].
Aboud, Heba M. ;
El Komy, Mohammed H. ;
Ali, Adel A. ;
El Menshawe, Shahira F. ;
Abd Elbary, Ahmed .
AAPS PHARMSCITECH, 2016, 17 (06) :1353-1365
[2]   Mechanisms of phagocytosis in macrophages [J].
Aderem, A ;
Underhill, DM .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :593-623
[3]  
Adib ZM, 2016, ADV PHARM BULL, V6, P31, DOI [10.15171/apb.2016.006, 10.15171/apb.2016.06]
[4]   Quality by Design Approach for Development and Characterisation of Solid Lipid Nanoparticles of Quetiapine Fumarate [J].
Agarwal, Shweta ;
Murthy, Rayasa S. Ramachandra ;
Harikumar, Sasidharan Leelakumari ;
Garg, Rajeev .
CURRENT COMPUTER-AIDED DRUG DESIGN, 2020, 16 (01) :73-91
[5]   Cutaneous Delivery of Natural Antioxidants: The Enhancement Approaches [J].
Aljuffali, Ibrahim A. ;
Hsu, Ching-Yun ;
Lin, Yin-Ku ;
Fang, Jia-You .
CURRENT PHARMACEUTICAL DESIGN, 2015, 21 (20) :2745-2757
[6]   Nanomedicines for overcoming biological barriers [J].
Alonso, MJ .
BIOMEDICINE & PHARMACOTHERAPY, 2004, 58 (03) :168-172
[7]  
[Anonymous], 2018, TRANSDERMAL
[8]   Formulation and in-vivo Evaluation of Novel Topical Gel of Lopinavir for Targeting HIV [J].
Ansari, Huda ;
Singh, Prabha .
CURRENT HIV RESEARCH, 2018, 16 (04) :270-279
[9]  
Attama Anthony A, 2011, Recent Pat Drug Deliv Formul, V5, P178
[10]   Lipid nanoparticles: state of the art, new preparation methods and challenges in drug delivery [J].
Battaglia, Luigi ;
Gallarate, Marina .
EXPERT OPINION ON DRUG DELIVERY, 2012, 9 (05) :497-508