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1.
Appl Biochem Biotechnol ; 172(3): 1574-84, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24233543

RESUMO

Supermacroporous poly(2-hydroxyethyl methacrylate-co-1,5-naphthalene bismaleimide) [poly(HEMA-co-NBMI)] monolithic cryogel column was prepared by free radical cryo-copolymerization of HEMA with NBMI as a hydrophobic functional comonomer and N,N'-methylene-bisacrylamide as cross-linker directly in a plastic syringe for adsorption of albumin. The monolithic cryogel contained a continuous polymeric matrix which has interconnected pores of 10-100 µm size. Poly(HEMA-co-NBMI) cryogel was characterized by swelling studies, FTIR and scanning electron microscopy. The equilibrium swelling degree of the poly(HEMA-co-NBMI) cryogel was 10.5 g of H2O/g dry cryogel. Poly(HEMA-co-NBMI) cryogel was used in the adsorption/desorption of IgG from aqueous solutions. The maximum amount of IgG adsorption from aqueous solution in phosphate buffer was 98.20 mg/g polymer at pH 7.0. The nonspecific adsorption of IgG onto plain poly(HEMA) cryogel was very low (2.79 g/g polymer). It was observed that IgG could be repeatedly adsorbed and desorbed with the poly(HEMA-co-NBMI) cryogel without significant loss of adsorption capacity.


Assuntos
Criogéis/química , Imunoglobulina G/química , Poli-Hidroxietil Metacrilato/química , Adsorção , Humanos , Interações Hidrofóbicas e Hidrofílicas , Imunoglobulina G/isolamento & purificação , Microscopia Eletrônica de Varredura , Polimerização
2.
J Labelled Comp Radiopharm ; 56(14): 708-16, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-24339009

RESUMO

In this study, N-methacryloyl-l-phenylalanine (MAPA) containing poly(2-hydroxyethylmethacrylate) (HEMA)-based magnetic poly(HEMA-MAPA) nanobeads [mag-poly(HEMA-MAPA)] were radiolabeled with (131) I [(131) I-mag-poly(HEMA-MAPA)], and the radiopharmaceutical potential of (131) I-mag-poly(HEMA-MAPA) was investigated. Quality control studies were carried out by radiochromatographic method to be sure that (131) I binded to mag-poly(HEMA-MAPA) efficiently. In this sense, binding yield of (131) I-mag-poly(HEMA-MAPA) was found to be about 95-100%. In addition to this, optimum radiodination conditions for (131) I-mag-poly(HEMA-MAPA) were determined by thin-layer radiochromatography studies. In addition to thin-layer radiochromatography studies, lipophilicity (partition coefficient) and stability studies for (131) I-mag-poly(HEMA-MAPA) were realized. It was determined that lipophilicities of mag-poly(HEMA-MAPA) and (131) I-mag-poly(HEMA-MAPA) were 0.12 ± 0.01 and 1.79 ± 0.76 according to ACD/logP algorithm program, respectively. Stability of the radiolabeled compound was investigated in time intervals given as 0, 30, 60, 180, and 1440 min. It was found that (131) I-mag-poly(HEMA-MAPA) existed as a stable complex in rat serum within 60 min. After that, biodistribution and scintigraphy studies were carried out by using albino Wistar rats. It was determined that the most important (131) I activity uptake was observed in the breast, the ovary, and the pancreas. Scintigraphy studies well supported biodistribution results.


Assuntos
Radioisótopos do Iodo/química , Nanopartículas de Magnetita/química , Poli-Hidroxietil Metacrilato/química , Compostos Radiofarmacêuticos/síntese química , Albinismo , Animais , Marcação por Isótopo , Fenilalanina/análogos & derivados , Fenilalanina/química , Compostos Radiofarmacêuticos/farmacocinética , Ratos , Ratos Wistar , Distribuição Tecidual
3.
Appl Biochem Biotechnol ; 162(8): 2232-43, 2010 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20521122

RESUMO

Supermacroporous poly{2-hydroxyethyl methacrylate-co-[N,N-bis(2,6-diisopropylphenyl)-perylene-3,4,9,10-tetracarboxylic diimide]} [poly(HEMA-co-DIPPER)] monolithic cryogel column was prepared by radical cryocopolymerization of HEMA with DIPPER as functional comonomer and N,N'-methylene-bisacrylamide (MBAAm) as crosslinker directly in a plastic syringe for adsorption of albumin. The monolithic cryogel contained a continuous polymeric matrix having interconnected pores of 10-50 µm size. Poly(HEMA-co-DIPPER) cryogel was characterized by swelling studies, FTIR, scanning electron microscopy, and elemental analysis. The equilibrium swelling degree of the poly(HEMA-co-DIPPER) cryogel was 14.7 g H2O/g dry cryogel. Poly(HEMA-co-DIPPER) cryogel was used in the adsorption/desorption of albumin from aqueous solutions. The nonspecific adsorption of albumin onto plain poly(HEMA) cryogel was very low (3.36 g/g polymer). The maximum amount of albumin adsorption from aqueous solution in acetate buffer was 40.9 mg/g polymer at pH 5.0. It was observed that albumin could be repeatedly adsorbed and desorbed with the poly(HEMA-co-DIPPER) cryogel without significant loss of adsorption capacity.


Assuntos
Albuminas/química , Hidrogéis/química , Interações Hidrofóbicas e Hidrofílicas , Adsorção , Criogéis , Cinética , Microscopia Eletrônica de Varredura , Concentração Osmolar , Polímeros/química , Porosidade , Espectroscopia de Infravermelho com Transformada de Fourier , Água/química
4.
Nucl Med Biol ; 35(4): 481-92, 2008 May.
Artigo em Inglês | MEDLINE | ID: mdl-18482686

RESUMO

The metabolic comparison of aniline- and phenol-phthaleins radiolabeled with (131)I ((131)I-APH and (131)I-PPH, respectively) has been investigated in this study. To compare the metabolic behavior of these phthaleins and their glucuronide conjugates radiolabeled with (131)I, scintigraphic and biodistributional techniques were applied using male Albino rabbits. The results obtained have shown that these compounds were successfully radioiodinated with a radioiodination yield of about 100%. Maximum uptakes of (131)I-APH and (131)I-PPH, which were metabolized as N- and O-glucuronides, were observed within 2 h in the bladder and in the small intestine, respectively. In the case of verification of considerably up taking of these compounds also by tumors developed in the small intestine and in the bladder tissues, these results can be expected to be encouraging to test these compounds, which will be radiolabeled with other radioiodines such as (125)I, (123)I and (124)I as imaging and therapeutic agents in nuclear medical applications.


Assuntos
Compostos de Anilina/farmacocinética , Neoplasias Intestinais/diagnóstico por imagem , Fenolftaleína/farmacocinética , Neoplasias da Bexiga Urinária/diagnóstico por imagem , Compostos de Anilina/síntese química , Animais , Cromatografia Líquida , Glucuronídeos/química , Glucuronídeos/farmacocinética , Intestino Delgado/diagnóstico por imagem , Intestino Delgado/patologia , Radioisótopos do Iodo/química , Radioisótopos do Iodo/farmacocinética , Masculino , Espectrometria de Massas , Fenolftaleína/química , Coelhos , Cintilografia , Compostos Radiofarmacêuticos/síntese química , Compostos Radiofarmacêuticos/farmacocinética , Espectrofotometria , Distribuição Tecidual , Bexiga Urinária/diagnóstico por imagem , Bexiga Urinária/patologia
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