Lipid nanoparticles for cancer therapy: state of the art and future prospects

被引:64
作者
Lasa-Saracibar, Beatriz [1 ]
Estella-Hermoso de Mendoza, Ander [1 ]
Guada, Melissa [1 ]
Dios-Vieitez, Carmen [1 ]
Blanco-Prieto, Maria J. [1 ]
机构
[1] Univ Navarra, Sch Pharm, Dept Pharm & Pharmaceut Technol, E-31080 Pamplona, Spain
关键词
anticancer therapy; lipid nanoparticles; nanomedicine; nanotechnology; tumor targeting; CONTROLLED DRUG-DELIVERY; IN-VITRO CYTOTOXICITY; ANTITUMOR-ACTIVITY; COACERVATION TECHNIQUE; TISSUE DISTRIBUTION; TRIGLYCERIDE NANOPARTICLES; MULTIDRUG-RESISTANCE; P-GLYCOPROTEIN; GENE DELIVERY; CELL UPTAKE;
D O I
10.1517/17425247.2012.717928
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Cancer is a leading cause of death worldwide and it is estimated that deaths from this disease will rise to over 11 million in 2030. Most cases of cancer can be cured with surgery, radiotherapy or chemotherapy if they are detected at an early stage. However, current cancer therapies are commonly associated with undesirable side effects, as most chemotherapy treatments are cytotoxic and present poor tumor targeting. Areas covered: Lipid nanoparticles (LN) are one of the most promising options in this field. LN are made up of biodegradable generally recognized as safe (GRAS) lipids, their formulation includes different techniques, and most are easily scalable to industrial manufacture. LN overcome the limitations imposed by the need for intravenous administration, as they are mainly absorbed via the lymphatic system when they are administered orally, which improves drug bioavailability. Furthermore, depending on their composition, LN present the ability to cross the blood-brain barrier, thus opening up the possibility of targeting brain tumors. Expert opinion: The drawbacks of chemotherapeutic agents make it necessary to invest in research to find safer and more effective therapies. Nanotechnology has opened the door to new therapeutic options through the design of formulations that include a wide range of materials and formulations at the nanometer range, which improve drug efficacy through direct or indirect tumor targeting, increased bioavailability and diminished toxicity.
引用
收藏
页码:1245 / 1261
页数:17
相关论文
共 145 条
[1]   Enhancement of Intestinal Permeability Utilizing Solid Lipid Nanoparticles Increases γ-Tocotrienol Oral Bioavailability [J].
Abuasal, Bilal S. ;
Lucas, Courtney ;
Peyton, Breanne ;
Alayoubi, Alaadin ;
Nazzal, Sami ;
Sylvester, Paul W. ;
Kaddoumi, Amal .
LIPIDS, 2012, 47 (05) :461-469
[2]   Cationic ligand appended nanoconstructs: A prospective strategy for brain targeting [J].
Agarwal, Abhinav ;
Agrawal, Himanshu ;
Tiwari, Shailja ;
Jain, Sanyog ;
Agrawal, Govind P. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 421 (01) :189-201
[3]   Lopinavir loaded solid lipid nanoparticles (SLN) for intestinal lymphatic targeting [J].
Alex, M. R. Aji ;
Chacko, A. J. ;
Jose, S. ;
Souto, E. B. .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2011, 42 (1-2) :11-18
[4]   Preparation, characterization, and anticancer effects of simvastatin-tocotrienol lipid nanoparticles [J].
Ali, Hazem ;
Shirode, Amit B. ;
Sylvester, Paul W. ;
Nazzal, Sami .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 389 (1-2) :223-231
[5]   LONG-CIRCULATING (STERICALLY STABILIZED) LIPOSOMES FOR TARGETED DRUG-DELIVERY [J].
ALLEN, TM .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1994, 15 (07) :215-220
[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]  
Altmayer P, 1993, Anasthesiol Intensivmed Notfallmed Schmerzther, V28, P415
[8]   5-Fluorouracil derivatives: a patent review [J].
Alvarez, Pablo ;
Antonio Marchal, Juan ;
Boulaiz, Houria ;
Carrillo, Esmeralda ;
Velez, Celia ;
Rodriguez-Serrano, Fernando ;
Melguizo, Consolacion ;
Prados, Jose ;
Madeddu, Roberto ;
Aranega, Antonia .
EXPERT OPINION ON THERAPEUTIC PATENTS, 2012, 22 (02) :107-123
[9]  
American cancer society, 2010, AM CANC SOC OV CANC
[10]  
American Cancer Society, 2012, BREAST CANC