Platinum Formulations as Anticancer Drugs Clinical and Pre-Clinical Studies

被引:69
作者
Farrell, Nicholas P. [1 ]
机构
[1] Virginia Commonwealth Univ, Dept Chem, Richmond, VA 23284 USA
关键词
Platinum anti-cancer agents; formulation; polymer drug delivery; nanomedicine; LIPOSOMAL CISPLATIN LIPOPLATIN; ANTITUMOR-ACTIVITY; PHASE-I; GOLD NANOPARTICLES; POLYMERIC MICELLES; SOLID TUMORS; CANCER; DELIVERY; TOXICITY; BINDING;
D O I
10.2174/156802611798040714
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This review summarizes clinical and pre-clinical results on platinum anti-cancer drug formulations. A concise summary of the use of oxidation state to modulate cancer pharmacology is given for Pt(IV) complexes, distinct from the clinically used Pt(II) drugs. The chemistry of platinum drug formulation combines aspects of kinetics of active moiety release from nominally weak-binding ligands (bond cleavage from platinum-carboxylate and platinum-phosphate) in polymers and nanoparticles with pharmacological considerations of plasma distribution and cellular accumulation. The action of any molecular entity as a drug is influenced by its ADME profile - absorption, distribution, metabolism and excretion. The purpose of drug formulation is to alter any or all of these parameters with the ultimate goal of improving the efficacy and reducing side effects with the possibility to target drugs directly to the tumor site. The diverse array of approaches includes liposomes, polymers (not limited to peptides, dendrimers, biodegradable polymers, polysaccharides, and metallic nanoparticles). Functionalization of the surfaces of nanoparticles with antibodies or cellular surface recognition motifs may further target specific cancers.
引用
收藏
页码:2623 / 2631
页数:9
相关论文
共 102 条
[1]  
AISEN P, 1994, ADV EXP MED BIOL, V356, P31
[2]   Factors affecting the clearance and biodistribution of polymeric nanoparticles [J].
Alexis, Frank ;
Pridgen, Eric ;
Molnar, Linda K. ;
Farokhzad, Omid C. .
MOLECULAR PHARMACEUTICS, 2008, 5 (04) :505-515
[3]   Rational design of platinum(IV) compounds to overcome glutathione-S-transferase mediated drug resistance [J].
Ang, WH ;
Khalaila, I ;
Allardyce, CS ;
Juillerat-Jeanneret, L ;
Dyson, PJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (05) :1382-1383
[4]   Activity of lipoplatin in tumor and in normal cells in vitro [J].
Arienti, Chiara ;
Tesei, Anna ;
Ravaioli, Alberto ;
Ratta, Marina ;
Carloni, Silvia ;
Mangianti, Serena ;
Ulivi, Paola ;
Nicoletti, Stefania ;
Amadori, Dino ;
Zoli, Wainer .
ANTI-CANCER DRUGS, 2008, 19 (10) :983-990
[5]   Polymer-Cisplatin Conjugate Nanoparticles for Acid-Responsive Drug Delivery [J].
Aryal, Santosh ;
Hu, Che-Ming Jack ;
Zhang, Liangfang .
ACS NANO, 2010, 4 (01) :251-258
[6]   Cucurbituril binding of trans-[{PtCl(NH3)2}2(μ-NH2(CH2)8NH2)]2+ and the effect on the reaction with cysteine [J].
Bali, Mark S. ;
Buck, Damian P. ;
Coe, Andrew J. ;
Day, Anthony I. ;
Collins, J. Grant .
DALTON TRANSACTIONS, 2006, (45) :5337-5344
[7]  
Bender M.L., 1978, Cyclodextrin chemistry
[8]   Satraplatin: leading the new generation of oral platinum agents [J].
Bhargava, Ashish ;
Vaishampayan, Ulka N. .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2009, 18 (11) :1787-1797
[9]  
Boulikas T, 2005, ANTICANCER RES, V25, P3031
[10]  
Boulikas T, 2004, ONCOL REP, V12, P3