Recent advances and future directions in amphiphilic cyclodextrin nanoparticles

被引:94
作者
Bilensoy, Erem [1 ]
Hincal, A. Atilla [1 ]
机构
[1] Hacettepe Univ, Fac Pharm, Dept Pharmaceut Technol, TR-06100 Ankara, Turkey
关键词
amphiphilic cyclodextrin; encapsulation; nanoparticle; preparation; synthesis; PROGESTERONE INCLUSION COMPLEXES; HYDROXYPROPYL-BETA-CYCLODEXTRIN; LANGMUIR-BLODGETT-FILMS; PHARMACEUTICAL APPLICATIONS; ALPHA-CYCLODEXTRIN; DRUG-DELIVERY; GENE DELIVERY; PHYSICOCHEMICAL PROPERTIES; ORAL BIOAVAILABILITY; ANIONIC PORPHYRINS;
D O I
10.1517/17425240903222218
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cyclodextrins are known to be promising excipients in the pharmaceutical industry, with their ability to include hydrophobic guest molecules masking the physicochemical properties of the guest, such as poor water solubility, stability problems and undesired side effects. These enabling excipients, which are produced on a large scale and incorporated into various marketed products worldwide, are now modified to render amphiphilic properties that enable them to be used to prepare nanoparticles. Amphiphilic cyclodextrins have the ability to form nanoparticles without the presence of a surfactant by different preparation techniques that are discussed in this review. Classification and physicochemical properties of these interesting molecules as well as the efficacy and safety of nanoparticles prepared from different amphiphilic cyclodextrins are discussed in light of the current literature work with in vitro and in vivo findings. Cyclodextrin nanoparticles of different nature effectively carry drugs or molecules with bioavailability problems arising from poor aqueous solubility, stability under physiological conditions or side effects associated with the molecule itself or excipients used in the formulation of these problems drugs. In conclusion, amphiphilic cyclodextrins emerge as promising alternatives for tumor drug delivery and passive and active targeting with non-toxic, non-hemolytic properties as injectable, nanosized carriers.
引用
收藏
页码:1161 / 1173
页数:13
相关论文
共 98 条
[31]  
Friedland R., 1991, NEW I ORG ANAL, P157
[32]   Conjugates of poly(DL-lactide-co-glycolide) on amino cyclodextrins and their nanoparticles as protein delivery system [J].
Gao, Hui ;
Wang, Yi-Nong ;
Fan, Yun-Ge ;
Ma, Jian-Biao .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2007, 80A (01) :111-122
[33]   Conjugates of poly(DL-lactic acid) with ethylenediamino or diethylenetriamino bridged bis(β-cyclodextrin)s and their nanoparticles as protein delivery systems [J].
Gao, Hui ;
Yang, Ying-wei ;
Fan, Yun-ge ;
Ma, Jian-biao .
JOURNAL OF CONTROLLED RELEASE, 2006, 112 (03) :301-311
[34]   Biodistribution of intravenously administered amphiphilic β-cyclodextrin nanospheres [J].
Geze, A. ;
Chau, L. Tieu ;
Choisnard, L. ;
Mathieu, J.-P. ;
Marti-Batlle, D. ;
Riou, L. ;
Putaux, J.-L. ;
Wouessidjewe, D. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 344 (1-2) :135-142
[35]   Novel nanoparticles made from amphiphilic perfluoroalkyl α-cyclodextrin derivatives: Preparation, characterization and application to the transport of acyclovir [J].
Ghera, Bernard Bertino ;
Perret, Florent ;
Chevalier, Yves ;
Parrot-Lopez, Helene .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2009, 375 (1-2) :155-162
[36]   Fluorine containing β-cyclodextrin:: a new class of amphiphilic carriers [J].
Granger, CE ;
Félix, CP ;
Parrot-Lopez, HP ;
Langlois, BR .
TETRAHEDRON LETTERS, 2000, 41 (48) :9257-9260
[38]   Effects of structure of β-cyclodextrin-containing polymers on gene delivery [J].
Hwang, SJ ;
Bellocq, NC ;
Davis, ME .
BIOCONJUGATE CHEMISTRY, 2001, 12 (02) :280-290
[39]   FORMATION AND DEPOSITION OF MONOLAYERS OF AMPHIPHILIC BETA-CYCLODEXTRIN DERIVATIVES [J].
KAWABATA, Y ;
MATSUMOTO, M ;
TANAKA, M ;
TAKAHASHI, H ;
IRINATSU, Y ;
TAMURA, S ;
TAGAKI, W ;
NAKAHARA, H ;
FUKUDA, K .
CHEMISTRY LETTERS, 1986, (11) :1933-1934
[40]   COMPLEX-FORMATION OF MODIFIED CYCLODEXTRINS WITH ORGANIC SALTS IN ORGANIC-SOLVENTS [J].
KOMIYAMA, M ;
YAMAMOTO, H ;
HIRAI, H .
CHEMISTRY LETTERS, 1984, (07) :1081-1084