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Items: 1 to 20 of 96

1.

Novel aldehyde-terminated dendrimers; synthesis and cytotoxicity assay.

Hamidi A, Sharifi S, Davaran S, Ghasemi S, Omidi Y, Rashidi MR.

Bioimpacts. 2012;2(2):97-103. doi: 10.5681/bi.2012.014.

2.

Effects of PAMAM dendrimers with various surface functional groups and multiple generations on cytotoxicity and neuronal differentiation using human neural progenitor cells.

Zeng Y, Kurokawa Y, Win-Shwe TT, Zeng Q, Hirano S, Zhang Z, Sone H.

J Toxicol Sci. 2016;41(3):351-70. doi: 10.2131/jts.41.351.

3.

Two for the Price of One: PAMAM-Dendrimers with Mixed Phosphoryl Choline and Oligomeric Poly(Caprolactone) Surfaces.

Svenningsen SW, Janaszewska A, Ficker M, Petersen JF, Klajnert-Maculewicz B, Christensen JB.

Bioconjug Chem. 2016 Jun 15;27(6):1547-57. doi: 10.1021/acs.bioconjchem.6b00213.

PMID:
27244598
4.

Interaction of poly(amidoamine) dendrimers with supported lipid bilayers and cells: hole formation and the relation to transport.

Hong S, Bielinska AU, Mecke A, Keszler B, Beals JL, Shi X, Balogh L, Orr BG, Baker JR Jr, Banaszak Holl MM.

Bioconjug Chem. 2004 Jul-Aug;15(4):774-82.

PMID:
15264864
5.

Selective cytotoxicity of PAMAM G5 core--PAMAM G2.5 shell tecto-dendrimers on melanoma cells.

Schilrreff P, Mundiña-Weilenmann C, Romero EL, Morilla MJ.

Int J Nanomedicine. 2012;7:4121-33. doi: 10.2147/IJN.S32785.

6.

Surface acetylation of polyamidoamine (PAMAM) dendrimers decreases cytotoxicity while maintaining membrane permeability.

Kolhatkar RB, Kitchens KM, Swaan PW, Ghandehari H.

Bioconjug Chem. 2007 Nov-Dec;18(6):2054-60.

PMID:
17960872
8.

Preparation and in vitro characterization of pluronic-attached polyamidoamine dendrimers for drug delivery.

Gu Z, Wang M, Fang Q, Zheng H, Wu F, Lin D, Xu Y, Jin Y.

Drug Dev Ind Pharm. 2015 May;41(5):812-8. doi: 10.3109/03639045.2014.908899.

PMID:
24745851
9.

Solubility of nicotinic acid in polyamidoamine dendrimer solutions.

Yiyun C, Tongwen X.

Eur J Med Chem. 2005 Dec;40(12):1384-9.

PMID:
16226352
10.
11.

Zwitterionic chitosan-polyamidoamine dendrimer complex nanoparticles as a pH-sensitive drug carrier.

Liu KC, Yeo Y.

Mol Pharm. 2013 May 6;10(5):1695-704. doi: 10.1021/mp300522p.

12.

Poly(amido amine) dendrimers as absorption enhancers for oral delivery of camptothecin.

Sadekar S, Thiagarajan G, Bartlett K, Hubbard D, Ray A, McGill LD, Ghandehari H.

Int J Pharm. 2013 Nov 1;456(1):175-85. doi: 10.1016/j.ijpharm.2013.07.071.

13.

Synthesis of new polymer-bound adenine nucleotides using starburst PAMAM dendrimers.

Abdelmoez W, Yasuda M, Ogino H, Ishimi K, Ishikawa H.

Biotechnol Prog. 2002 Jul-Aug;18(4):706-12.

PMID:
12153302
14.

PEGylated, NH2-terminated PAMAM dendrimers: a microscopic view from atomistic computer simulations.

Yang L, da Rocha SR.

Mol Pharm. 2014 May 5;11(5):1459-70. doi: 10.1021/mp400630z.

PMID:
24679335
15.

Synthesis and characterization of dendritic star-shaped zwitterionic polymers as novel anticancer drug delivery carriers.

Li L, Wang Y, Ji F, Wen Y, Li J, Yang B, Yao F.

J Biomater Sci Polym Ed. 2014;25(14-15):1641-57. doi: 10.1080/09205063.2014.936994.

PMID:
25025700
16.

Cytotoxicity and in vitro characterization studies of synthesized Jeffamine-cored PAMAM dendrimers.

Oztürk K, Ertürk AS, Sarısözen C, Tulu M, Calış S.

J Microencapsul. 2014;31(2):127-36. doi: 10.3109/02652048.2013.814727.

PMID:
23862724
17.

The effect of PAMAM dendrimer generation size and surface functional group on the aqueous solubility of nifedipine.

Devarakonda B, Hill RA, de Villiers MM.

Int J Pharm. 2004 Oct 13;284(1-2):133-40.

PMID:
15454304
18.

In vitro dose-response effects of poly(amidoamine) dendrimers [amino-terminated and surface-modified with N-(2-hydroxydodecyl) groups] and quantitative determination by a liquid chromatography-hybrid quadrupole/time-of-flight mass spectrometry based method.

Hernando MD, Rosenkranz P, Ulaszewska MM, Fernández-Cruz ML, Fernández-Alba AR, Navas JM.

Anal Bioanal Chem. 2012 Nov;404(9):2749-63. doi: 10.1007/s00216-012-6256-4.

PMID:
22875538
19.

Effect of Terminal Groups of Dendrimers in the Complexation with Antisense Oligonucleotides and Cell Uptake.

Márquez-Miranda V, Peñaloza JP, Araya-Durán I, Reyes R, Vidaurre S, Romero V, Fuentes J, Céric F, Velásquez L, González-Nilo FD, Otero C.

Nanoscale Res Lett. 2016 Dec;11(1):66. doi: 10.1186/s11671-016-1260-9.

20.

Amino acid-functionalized dendrimers with heterobifunctional chemoselective peripheral groups for drug delivery applications.

Navath RS, Menjoge AR, Wang B, Romero R, Kannan S, Kannan RM.

Biomacromolecules. 2010 Jun 14;11(6):1544-63. doi: 10.1021/bm100186b.

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