نتایج جستجو برای: g5 pamam dendrimers

تعداد نتایج: 4698  

Journal: :International Journal of Nanomedicine 2007
Hu Yang Weiyuan John Kao

Spatial control over the distribution and the aggregation of arginine-glycine-aspartate (RGD) peptides at the nanoscale significantly affects cell responses. For example, nanoscale clustering of RGD peptides can induce integrins to cluster, thus triggering complete cell signaling. Dendrimers have a unique, highly branched, nearly spherical and symmetrical structure with low polydispersity, nano...

Journal: :Chemical communications 2008
Guangnan Ou Li Xu Biyan He Youzhu Yuan

Highly stable dendrimer-encapsulated Pd nanoparticles in ionic liquids were prepared for the first time by using charged PAMAM dendrimers as templates, which could maintain hydrogenation efficiency for up to at least 12 recycles.

Journal: :Chemical communications 2005
Jakub Rudovsky Petr Hermann Mauro Botta Silvio Aime Ivan Lukes

A marked increase of relaxivity has been observed upon rigidifying the internal frame of Gd-containing PAMAM dendrimers: the effect has been attained by either protonation of the dendrimer or by forming supramolecular adducts with cationic polyaminoacids.

2011
Mengen Zhang Rui Guo Yin Wang Xueyan Cao Mingwu Shen Xiangyang Shi

BACKGROUND We report here a unique approach to using multifunctional dendrimer/combretastatin A4 (CA4) inclusion complexes for targeted cancer therapeutics. METHODS Amine-terminated generation 5 polyamidoamine dendrimers were first partially acetylated to neutralize a significant portion of the terminal amines, and then the remaining dendrimer terminal amines were sequentially modified with f...

Journal: :Bioconjugate chemistry 2011
Hubert F Gaertner Fabrice Cerini Arun Kamath Anne-Françoise Rochat Claire-Anne Siegrist Laure Menin Oliver Hartley

Nanoparticles carrying biologically active functional sets (e.g., targeting moiety, payload, tracer) have potential use in a wide range of clinical applications. Though complex, such constructions should, as far as possible, have a defined molecular architecture and be monodisperse. However, the existing methods to achieve this goal are unsuitable for the incorporation of peptides and proteins,...

Journal: :The journal of physical chemistry. B 2008
Christopher V Kelly Pascale R Leroueil Bradford G Orr Mark M Banaszak Holl Ioan Andricioaei

The molecular structures and enthalpy release of poly(amidoamine) (PAMAM) dendrimers binding to 1,2-dimyristoyl- sn-glycero-3-phosphocholine (DMPC) bilayers were explored through atomistic molecular dynamics. Three PAMAM dendrimer terminations were examined: protonated primary amine, neutral acetamide, and deprotonated carboxylic acid. Fluid and gel lipid phases were examined to extract the eff...

Journal: :Chemical communications 2011
Patricia Anne A Ignacio-de Leon Ilya Zharov

Diffusion rate of dye-labelled PAMAM dendrimers through free-standing silica colloidal crystals was studied as a function of the dendrimer generation and nanopore size to determine the transport selectivity.

2014
Mallory A. van Dongen Rahul Rattan Justin Silpe Casey Dougherty Nicole L. Michmerhuizen Margaret Van Winkle Baohua Huang Seok Ki Choi Kumar Sinniah Bradford G. Orr Mark M. Banaszak Holl

Generation 5 poly(amidoamine) (G5 PAMAM) methotrexate (MTX) conjugates employing two small molecular linkers, G5-(COG-MTX)n, G5-(MFCO-MTX)n were prepared along with the conjugates of the G5-G5 (D) dimer, D-(COG-MTX)n, D-(MFCO-MTX)n. The monomer G5-(COG-MTX)n conjugates exhibited only a weak, rapidly reversible binding to folate binding protein (FBP) consistent with monovalent MTX binding. The D...

Journal: :Nanoscale 2015
Jingyi Zhu Lingzhou Zhao Yongjun Cheng Zhijuan Xiong Yueqin Tang Mingwu Shen Jinhua Zhao Xiangyang Shi

We report the synthesis, characterization, and utilization of radioactive (131)I-labeled multifunctional dendrimers for targeted single-photon emission computed tomography (SPECT) imaging and radiotherapy of tumors. In this study, amine-terminated poly(amidoamine) dendrimers of generation 5 (G5·NH2) were sequentially modified with 3-(4'-hydroxyphenyl)propionic acid-OSu (HPAO) and folic acid (FA...

Journal: :Acta Biomaterialia 2021

The effective life-time of new antimicrobials until the appearance first resistant strains is steadily decreasing, which discourages incentives for commercialization required clinical translation and application. Therefore, development should not only focus on better killing antimicrobial-resistant strains, but as a paradigm shift developing that prevent induction resistance. Heterofunctionaliz...

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