Nanocarriers' entry into the cell: relevance to drug delivery

被引:1205
作者
Hillaireau, Herve [2 ]
Couvreur, Patrick [1 ]
机构
[1] Univ Paris 11, CNRS, IFR 141, Fac Pharm,UMR 8612, F-92296 Chatenay Malabry, France
[2] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
关键词
Liposomes; Nanoparticles; Polymeric micelles; Endocytosis; Phagocytosis; Clathrin; Caveolae; Macropinocytosis; RECEPTOR-MEDIATED ENDOCYTOSIS; DOXORUBICIN-LOADED NANOPARTICLES; PH-SENSITIVE LIPOSOMES; BLOOD-BRAIN-BARRIER; TUMORS IN-VIVO; FOLATE RECEPTOR; SURFACE-CHARGE; ANTISENSE OLIGONUCLEOTIDES; CHITOSAN NANOPARTICLES; SOLID TUMORS;
D O I
10.1007/s00018-009-0053-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nanocarriers offer unique possibilities to overcome cellular barriers in order to improve the delivery of various drugs and drug candidates, including the promising therapeutic biomacromolecules (i.e., nucleic acids, proteins). There are various mechanisms of nanocarrier cell internalization that are dramatically influenced by nanoparticles' physicochemical properties. Depending on the cellular uptake and intracellular trafficking, different pharmacological applications may be considered. This review will discuss these opportunities, starting with the phagocytosis pathway, which, being increasingly well characterized and understood, has allowed several successes in the treatment of certain cancers and infectious diseases. On the other hand, the non-phagocytic pathways encompass various complicated mechanisms, such as clathrin-mediated endocytosis, caveolae-mediated endocytosis and macropinocytosis, which are more challenging to control for pharmaceutical drug delivery applications. Nevertheless, various strategies are being actively investigated in order to tailor nanocarriers able to deliver anticancer agents, nucleic acids, proteins and peptides for therapeutic applications by these non-phagocytic routes.
引用
收藏
页码:2873 / 2896
页数:24
相关论文
共 215 条
[1]   How to eat something bigger than your head [J].
Aderem, A .
CELL, 2002, 110 (01) :5-8
[2]   Mechanisms of phagocytosis in macrophages [J].
Aderem, A ;
Underhill, DM .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :593-623
[3]   AmBisome: liposomal formulation, structure, mechanism of action and pre-clinical experience [J].
Adler-Moore, J ;
Proffitt, RT .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 :21-30
[4]   Development and brain delivery of chitosan-PEG nanoparticles functionalized with the monoclonal antibody OX26 [J].
Aktas, Y ;
Yemisci, M ;
Andrieux, K ;
Gürsoy, RN ;
Alonso, MJ ;
Fernandez-Megia, E ;
Novoa-Carballal, R ;
Quiñoá, E ;
Riguera, R ;
Sargon, MF ;
Çelik, HH ;
Demir, AS ;
Hincal, AA ;
Dalkara, T ;
Çapan, Y ;
Couvreur, P .
BIOCONJUGATE CHEMISTRY, 2005, 16 (06) :1503-1511
[5]   UPTAKE OF LIPOSOMES BY CULTURED MOUSE BONE-MARROW MACROPHAGES - INFLUENCE OF LIPOSOME COMPOSITION AND SIZE [J].
ALLEN, TM ;
AUSTIN, GA ;
CHONN, A ;
LIN, L ;
LEE, KC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1061 (01) :56-64
[6]   OPTIMIZATION AND UPSCALING OF DOXORUBICIN-CONTAINING LIPOSOMES FOR CLINICAL USE [J].
AMSELEM, S ;
GABIZON, A ;
BARENHOLZ, Y .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1990, 79 (12) :1045-1052
[7]   Biodegradation and biocompatibility of PLA and PLGA microspheres [J].
Anderson, JM ;
Shive, MS .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 28 (01) :5-24
[8]   TRANSMUCOSAL PASSAGE OF POLYALKYLCYANOACRYLATE NANOCAPSULES AS A NEW DRUG CARRIER IN THE SMALL-INTESTINE [J].
APRAHAMIAN, M ;
MICHEL, C ;
HUMBERT, W ;
DEVISSAGUET, JP ;
DAMGE, C .
BIOLOGY OF THE CELL, 1987, 61 (1-2) :69-76
[9]   Preparation and biological characterization of polymeric micelle drug carriers with intracellular pH-triggered drug release property: Tumor permeability, controlled subcellular drug distribution, and enhanced in vivo antitumor efficacy [J].
Bae, Y ;
Nishiyama, N ;
Fukushima, S ;
Koyama, H ;
Yasuhiro, M ;
Kataoka, K .
BIOCONJUGATE CHEMISTRY, 2005, 16 (01) :122-130
[10]   Endocytic mechanisms for targeted drug delivery [J].
Bareford, Lisa A. ;
Swaan, Peter W. .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (08) :748-758