Dendrimers as multi-purpose nanodevices for oncology drug delivery and diagnostic imaging

被引:389
作者
Tomalia, D. A.
Reyna, L. A.
Svenson, S.
机构
[1] Dendrit Nanotechnol Inc, Mt Pleasant, MI 48858 USA
[2] Cent Michigan Univ, Dept Chem, Mt Pleasant, MI 48859 USA
关键词
dendrimer; diagnostic imaging; nanocontainer; nanomedicine; nanoscaffolding; targeted delivery;
D O I
10.1042/BST0350061
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
Dendrimers are routinely synthesized as tuneable nanostructures that may be designed and regulated as a function of their size, shape, surface chemistry and interior void space. They are obtained with structural control approaching that of traditional biomacromolecules such as DNA/RNA or proteins and are distinguished by their precise nanoscale scaffolding and nanocontainer properties. As such, these important properties are expected to play an important role in the emerging field of nanomedicine. This review will describe progress on the use of these features for both targeted diagnostic imaging and drug-delivery applications. Recent efforts have focused on the synthesis and pre-clinical evaluation of a multipurpose STARBURST (R) PAMAM (polyamidoamine) dendrimer prototype that exhibits properties suitable for use as: (i) targeted, diagnostic MRI (magnetic resonance imaging)/NIR (near-IR) contrast agents, (ii) and/or for controlled delivery of cancer therapies. Special emphasis will be placed on the lead candidate, namely [core: 1,4-diaminobutane; G (generation) = 4.5], [dendri-PAMAM(CO2Na)(64)]. This dendritic nanostructure (i.e. similar to 5.0 nm diameter) was selected on the basis of a very favourable biocompatibility profile [The Nanotechnology Characterization Laboratory (NCL), an affiliate of the National Cancer Institute (NCI), has completed extensive in vitro studies on the lead compound and have found it to be very benign, non-immunogenic and highly biocompatible], the expectation that it will exhibit desirable mammalian kidney excretion properties and demonstrated targeting features.
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页码:61 / 67
页数:7
相关论文
共 49 条
[1]  
[Anonymous], 2001, DENDRIMERS OTHER DEN
[2]   Vascular endothelial growth factor selectively targets boronated dendrimers to tumor vasculature [J].
Backer, MV ;
Gaynutdinov, TI ;
Patel, V ;
Bandyopadhyaya, AK ;
Thirumamagal, BTS ;
Tjarks, W ;
Barth, RF ;
Claffey, K ;
Backer, JM .
MOLECULAR CANCER THERAPEUTICS, 2005, 4 (09) :1423-1429
[3]   The Synthesis and Testing of Anti-Cancer Therapeutic Nanodevices [J].
Baker, James R., Jr. ;
Quintana, Antonio ;
Piehler, Lars ;
Banazak-Holl, Mark ;
Tomalia, Donald ;
Raczka, Ewa .
BIOMEDICAL MICRODEVICES, 2001, 3 (01) :61-69
[4]   A PEGylated dendritic nanoparticulate carrier of fluorouracil [J].
Bhadra, D ;
Bhadra, S ;
Jain, S ;
Jain, NK .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 257 (1-2) :111-124
[5]   Dendrimers in drug research [J].
Boas, U ;
Heegaard, PMH .
CHEMICAL SOCIETY REVIEWS, 2004, 33 (01) :43-63
[6]  
Boas U, 2006, DENDRIMERS MED BIOTE
[7]   The use of a dendrimer-propranolol prodrug to bypass efflux transporters and enhance oral bioavailability [J].
D'Emanuele, A ;
Jevprasesphant, R ;
Penny, J ;
Attwood, D .
JOURNAL OF CONTROLLED RELEASE, 2004, 95 (03) :447-453
[8]   Transport mechanism(s) of poly (amidoamine) dendrimers across Caco-2 cell monolayers [J].
El-Sayed, M ;
Rhodes, CA ;
Ginski, M ;
Ghandehari, H .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 265 (1-2) :151-157
[9]   Poly(amidoamine) (PAMAM) dendrimers: from biomimicry to drug delivery and biomedical applications [J].
Esfand, R ;
Tomalia, DA .
DRUG DISCOVERY TODAY, 2001, 6 (08) :427-436
[10]   SPL7013 gel as a topical microbicide for prevention of vaginal transmission of SHIV89.6P in macaques [J].
Jiang, YH ;
Emau, P ;
Cairns, JS ;
Flanary, L ;
Morton, WR ;
McCarthy, TD ;
Tsai, CC .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 2005, 21 (03) :207-213