Advances and new technologies applied in controlled drug delivery system

被引:37
作者
Bassyouni, Fatma [1 ,2 ]
ElHalwany, Noha [3 ]
Rehim, Mohamed Abdel [4 ]
Neyfeh, Munir [5 ]
机构
[1] Natl Res Ctr, Ctr Excellence Adv Sci, Dept Chem Nat & Microbial Prod, Cairo 12622, Egypt
[2] Natl Res Ctr, Ctr Excellence Adv Sci, Dept Pharmaceut Res, Cairo 12622, Egypt
[3] Natl Res Ctr, Dept Polymers & Pigments, Cairo 12622, Egypt
[4] Stockholm Univ, Dept Analyt Chem, S-10691 Stockholm, Sweden
[5] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
关键词
Transdermal drug delivery; Colon delivery system; Liposomes; Nano-capsules; Carbon nanotubes; Hydrogels; FUNCTIONALIZED CARBON NANOTUBES; METHOXY POLY(ETHYLENE GLYCOL); BLOCK-COPOLYMER MICELLES; POLYION COMPLEX MICELLES; POLYMERIC MICELLES; CONTROLLED-RELEASE; POLYELECTROLYTE COMPLEXES; IN-VIVO; AMPHIPHILIC DIBLOCK; COLLOIDAL PARTICLES;
D O I
10.1007/s11164-013-1338-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A drug delivery system is defined as a formulation or a device that enables the introduction of a therapeutic substance into the body and improves its efficacy and safety by controlling the rate, time, and place of release of drugs in the body. This process includes the administration of the therapeutic product, the release of the active ingredients by the product, and the subsequent transport of the active ingredients across the biological membranes to the site of action. Drug delivery systems aim to improve patient compliance and convenience, such as, for example, fast-dissolving tablets. One of the most important goals of pharmaceutical science is localizing the pharmacological activity of the drug at the site of action. Drug delivery systems are molecular tools which, without undesired interactions at other sites, target a specific drug receptor. Keeping in view the advantages of the delivery system, rapidly disintegrating dosage forms have been successfully commercialized, and, because of increased patient demand, these dosage forms are expected to become more popular. Modern drug delivery technology has been made possible by advances in polymer science. These advances have resulted in polymers with unique properties. Drug delivery systems are made from a variety of organic and inorganic compounds such as polymers, lipids (liposomes, nanoemulsions, and solid-lipid nanoparticles), self-assembling amphiphilic molecules, dendrimers, and inorganic nanocrystals. In addition, hydrogels are novel delivery systems that have attracted much attention in current pharmaceutical research.
引用
收藏
页码:2165 / 2200
页数:36
相关论文
共 166 条
  • [1] Self-porating polymersomes of PEG-PLA and PEG-PCL: hydrolysis-triggered controlled release vesicles
    Ahmed, F
    Discher, DE
    [J]. JOURNAL OF CONTROLLED RELEASE, 2004, 96 (01) : 37 - 53
  • [2] Hydrogels as drug-delivery platforms: physicochemical barriers and solutions
    Alkayyali, Lamees B.
    Abu-Diak, Osama A.
    Andrews, Gavin P.
    Jones, David S.
    [J]. THERAPEUTIC DELIVERY, 2012, 3 (06) : 775 - 786
  • [3] Nano-engineering block copolymer aggregates for drug delivery
    Allen, C
    Maysinger, D
    Eisenberg, A
    [J]. COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 16 (1-4) : 3 - 27
  • [4] THE USE OF GLYCOLIPIDS AND HYDROPHILIC POLYMERS IN AVOIDING RAPID UPTAKE OF LIPOSOMES BY THE MONONUCLEAR PHAGOCYTE SYSTEM
    ALLEN, TM
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 1994, 13 (03) : 285 - 309
  • [5] Intelligent Drug Delivery Systems: Polymeric Micelles and Hydrogels
    Alvarez-Lorenzo, Carmen
    Concheiro, Angel
    [J]. MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2008, 8 (11) : 1065 - 1074
  • [6] Temperature- and light-responsive blends of pluronic F127 and Poly(N,N-dimethylacrylamide-co-methacryloyloxyazobenzene)
    Alvarez-Lorenzo, Carmen
    Deshmukh, Smeet
    Bromberg, Lev
    Hatton, T. Alan
    Sandez-Macho, Isabel
    Concheiro, Angel
    [J]. LANGMUIR, 2007, 23 (23) : 11475 - 11481
  • [7] Polyester-poly(ethylene glycol) nanoparticles loaded with the pure antiestrogen RU 58668: Physicochemical and opsonization properties
    Ameller, T
    Marsaud, R
    Legrand, P
    Gref, R
    Barratt, G
    Renoir, JM
    [J]. PHARMACEUTICAL RESEARCH, 2003, 20 (07) : 1063 - 1070
  • [8] Ansel HC, 2005, PHARM DOSAGE FORMS D
  • [9] Conductimetric study of the interpolyelectrolyte reaction between chitosan and polygalacturonic acid
    Argüelles-Monal, W
    Cabrera, G
    Peniche, C
    Rinaudo, M
    [J]. POLYMER, 2000, 41 (07) : 2373 - 2378
  • [10] ATTWOOD D., 2002, PHARM SCI DOSAGE FOR, V2nd