Cyclodextrins in drug delivery: An updated review

被引:942
作者
Challa, R [1 ]
Ahuja, A [1 ]
Ali, J [1 ]
Khar, RK [1 ]
机构
[1] Hamdard Univ, Fac Pharm, Dept Pharmaceut, New Delhi 110062, India
关键词
cyclodextrins; drug formulation; drug delivery; novel delivery systems; excipients;
D O I
10.1208/pt060243
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this review is to discuss and summarize some of the interesting findings and applications of cyclodextrins (CDs) and their derivatives in different areas of drug delivery, particularly in protein and peptide drug delivery and gene delivery. The article highlights important CD applications in the design of various novel delivery systems like liposomes, microspheres, microcapsules, and nanoparticles. In addition to their well-known effects on drug solubility and dissolution, bioavailability, safety, and stability, their use as excipients in drug formulation are also discussed in this article. The article also focuses on various factors influencing inclusion complex formation because an understanding of the same is necessary for proper handling of these versatile materials. Some important considerations in selecting CDs in drug formulation such as their commercial availability, regulatory status, and patent status are also summarized. CDs, because of their continuing ability to find several novel applications in drug delivery, are expected to solve many problems associated with the delivery of different novel drugs through different delivery routes.
引用
收藏
页数:29
相关论文
共 243 条
[31]   EVIDENCE FOR A POLARIZED EFFLUX SYSTEM FOR PEPTIDES IN THE APICAL MEMBRANE OF CACO-2 CELLS [J].
BURTON, PS ;
CONRADI, RA ;
HILGERS, AR ;
HO, NFH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 190 (03) :760-766
[32]  
Buschmann HJ, 2002, J COSMET SCI, V53, P185
[33]   Solubilization of tropicamide by hydroxypropyl-β-cyclodextrin and water-soluble polymers:: in vitro/in vivo studies [J].
Cappello, B ;
Carmignani, C ;
Iervolino, M ;
La Rotonda, MI ;
Saettone, MF .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 213 (1-2) :75-81
[34]   Preparation and characterization of albendazole β-cyclodextrin complexes [J].
Castillo, JA ;
Palomo-Canales, J ;
Garcia, JJ ;
Lastres, JL ;
Bolas, F ;
Torrado, JJ .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1999, 25 (12) :1241-1248
[35]   Improved dissolution behaviour of steam-granulated piroxicam [J].
Cavallari, C ;
Abertini, B ;
González-Rodríguez, ML ;
Rodriguez, L .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2002, 54 (01) :65-73
[36]   Solid lipid nanoparticles as carriers of hydrocortisone and progesterone complexes with β-cyclodextrins [J].
Cavalli, R ;
Peira, E ;
Caputo, O ;
Gasco, MR .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 182 (01) :59-69
[37]   Transdermal iontophoretic delivery of hydrocortisone from cyclodextrin solutions [J].
Chang, SL ;
Banga, AK .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1998, 50 (06) :635-640
[38]   Terfenadine-β-cyclodextrin inclusion complex with antihistaminic activity enhancement [J].
Choi, HG ;
Lee, BJ ;
Han, JH ;
Lee, MK ;
Park, KM ;
Yong, CS ;
Rhee, JD ;
Kim, YB ;
Kim, CK .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2001, 27 (08) :857-862
[39]  
Chowdary K. P. R., 2001, Indian Journal of Pharmaceutical Sciences, V63, P438
[40]   Nimesulide and β-cyclodextrin inclusion complexes:: Physicochemical characterization and dissolution rate studies [J].
Chowdary, KPR ;
Nalluri, BN .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2000, 26 (11) :1217-1220