Three generations of α,γ-diaminobutyric acid modified poly(propyleneimine) dendrimers and their cisplatin-type platinum complexes

被引:25
作者
Bellis, E.
Hajba, L.
Kovacs, B.
Sandor, K.
Kollar, L.
Kokotos, G.
机构
[1] Univ Pecs, Dept Inorgan Chem, H-7624 Pecs, Hungary
[2] Univ Athens, Organ Chem Lab, GR-15771 Athens, Greece
[3] Univ Veszprem, Dept Analyt Chem, H-8200 Veszprem, Hungary
[4] Univ Pecs, Dept Gen & Phys Chem, H-7624 Pecs, Hungary
[5] Hungarian Acad Sci, Res Grp Chem Sensors, H-7624 Pecs, Hungary
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2006年 / 69卷 / 1-2期
关键词
dendrimer; cisplatin; platinum; infrared spectroscopy;
D O I
10.1016/j.jbbm.2006.02.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Three generations of alpha,gamma-diaminobutyric acid modified poly(propyleneimine) dendrimers [DAB(AM)(n), n=4, 8, 16] containing 4, 8, 16 free amino groups were coupled with Boc-protected alpha,gamma-diaminobutyric acid (DABA) moieties in high yields. These modified dendrimers were deprotected and the chiral dendritic amines with 8, 16 and 32 amino groups on the surface were isolated in excellent yields. Dendrimers with cisplatin moieties at the periphery were obtained in the reaction of the free amine dendrimers and potassium tetrachloroplatinate(II). The highly insoluble complexes were isolated as hydrates and characterized by means of IR, TGA and elemental analysis. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:151 / 161
页数:11
相关论文
共 32 条
[1]   USE OF ESTERS OF N-HYDROXYSUCCINIMIDE IN PEPTIDE SYNTHESIS [J].
ANDERSON, GW ;
CALLAHAN, FM ;
ZIMMERMAN, JE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1964, 86 (09) :1839-+
[2]   Dendrimers as potential drug carriers; encapsulation of acidic hydrophobes within water soluble PAMAM derivatives [J].
Beezer, AE ;
King, ASH ;
Martin, IK ;
Mitchell, JC ;
Twyman, LJ ;
Wain, CF .
TETRAHEDRON, 2003, 59 (22) :3873-3880
[3]   Proline-modified poly (propyleneimine) dendrimers as catalysts for asymmetric aldol reactions [J].
Bellis, E ;
Kokotos, G .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2005, 241 (1-2) :166-174
[4]  
Bellis E, 2002, SYNTHESIS-STUTTGART, P1359
[5]   Dendrimer biocompatibility and toxicity [J].
Duncan, R ;
Izzo, L .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (15) :2215-2237
[6]   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
[7]  
Fischer M, 1999, ANGEW CHEM INT EDIT, V38, P885, DOI 10.1002/(SICI)1521-3773(19990401)38:7<884::AID-ANIE884>3.0.CO
[8]  
2-K
[9]  
Grinstaff MW, 2002, CHEM-EUR J, V8, P2838, DOI 10.1002/1521-3765(20020703)8:13<2838::AID-CHEM2838>3.0.CO
[10]  
2-I