Solid Lipid Nanoparticles: Emerging Colloidal Nano Drug Delivery Systems

被引:413
作者
Mishra, Vijay [1 ]
Bansal, Kuldeep K. [2 ]
Verma, Asit [1 ]
Yadav, Nishika [1 ]
Thakur, Sourav [1 ]
Sudhakar, Kalvatala [1 ]
Rosenholm, Jessica M. [2 ]
机构
[1] Lovely Profess Univ, Sch Pharmaceut Sci, Phagwara 144411, Punjab, India
[2] Abo Akad Univ, Pharmaceut Sci Lab, Fac Sci & Engn, FIN-20520 Turku, Finland
基金
芬兰科学院;
关键词
solid lipid nanoparticles; cytotoxicity; targeted drug delivery; colloidal nanocarriers; IN-VITRO; CELLULAR UPTAKE; ORAL DELIVERY; PHYSICOCHEMICAL CHARACTERIZATION; CARRIER SYSTEM; FORMULATION; CURCUMIN; CYTOTOXICITY; CANCER; SLN;
D O I
10.3390/pharmaceutics10040191
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Solid lipid nanoparticles (SLNs) are nanocarriers developed as substitute colloidal drug delivery systems parallel to liposomes, lipid emulsions, polymeric nanoparticles, and so forth. Owing to their unique size dependent properties and ability to incorporate drugs, SLNs present an opportunity to build up new therapeutic prototypes for drug delivery and targeting. SLNs hold great potential for attaining the goal of targeted and controlled drug delivery, which currently draws the interest of researchers worldwide. The present review sheds light on different aspects of SLNs including fabrication and characterization techniques, formulation variables, routes of administration, surface modifications, toxicity, and biomedical applications.
引用
收藏
页数:21
相关论文
共 98 条
[1]   Superparamagnetic Iron Oxidee-Loaded Lipid Nanocarriers Incorporated in Thermosensitive In Situ Gel for Magnetic Brain Targeting of Clonazepam [J].
Abbas, Haidy ;
Refai, Hanan ;
El Sayed, Nesrine .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2018, 107 (08) :2119-2127
[2]  
Abbasalipourkabir R., 2011, Biotechnology, V10, P528
[3]  
Adib ZM, 2016, ADV PHARM BULL, V6, P31, DOI [10.15171/apb.2016.06, 10.15171/apb.2016.006]
[4]   Solid Lipid Nanoparticles: A Potential Multifunctional Approach towards Rheumatoid Arthritis Theranostics [J].
Albuquerque, Joao ;
Moura, Catarina Costa ;
Sarmento, Bruno ;
Reis, Salette .
MOLECULES, 2015, 20 (06) :11103-11118
[5]   Lipid nanoparticles with minimum burst release of TNF-α siRNA show strong activity against rheumatoid arthritis unresponsive to methotrexate [J].
Aldayel, Abdulaziz M. ;
O'Mary, Hannah L. ;
Valdes, Solange A. ;
Li, Xu ;
Thakkar, Sachin G. ;
Mustafa, Bahar E. ;
Cui, Zhengrong .
JOURNAL OF CONTROLLED RELEASE, 2018, 283 :280-289
[6]   Solid lipid nanoparticles as a drug delivery system for peptides and proteins [J].
Almeida, Antonio J. ;
Souto, Eliana .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (06) :478-490
[7]   Effect of beeswax modification on the lipid matrix and solid lipid nanoparticle crystallinity [J].
Attama, Anthony A. ;
Mueller-Goymann, Christel C. .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2008, 315 (1-3) :189-195
[8]   Surface modification of solid lipid nanoparticles for oral delivery of curcumin: Improvement of bioavailability through enhanced cellular uptake, and lymphatic uptake [J].
Baek, Jong-Suep ;
Cho, Cheong-Weon .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2017, 117 :132-140
[9]   Renewable poly(δ-decalactone) based block copolymer micelles as drug delivery vehicle: in vitro and in vivo evaluation [J].
Bansal, Kuldeep K. ;
Gupta, Jitendra ;
Rosling, Ari ;
Rosenholm, Jessica M. .
SAUDI PHARMACEUTICAL JOURNAL, 2018, 26 (03) :358-368
[10]   Detergent-like actions of linear amphipathic cationic antimicrobial peptides [J].
Bechinger, Burkhard ;
Lohner, Karl .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (09) :1529-1539