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1.
Eksp Klin Farmakol ; 72(3): 29-32, 2009.
Artigo em Russo | MEDLINE | ID: mdl-19642589

RESUMO

A comparative analysis of the concentrations of acetylsalicylic acid (ASA) and its metabolite, salicylic acid (SA), in the blood was performed and the other pharmacokinetic parameters were studied after conventional intragastric and transdermal administration in rabbits. It is established that the ASA concentration in the blood upon transdermal administration in a dose of 100 mg/kg is above the minimum therapeutic level during 24 h. Prolonged action of a transdermal therapeutic system (TTS) in comparison to intragastric administration was proved. After the transdermal administration via TTS, the ASA half-elimination time and the mean retention time increased in comparison to the values upon intragastric administration. The ASA bioavailability upon the transdermal administration increased by a factor of 4.5 in comparison to the case of peroral administration.


Assuntos
Aspirina/administração & dosagem , Inibidores da Agregação Plaquetária/administração & dosagem , Ácido Salicílico/metabolismo , Administração Cutânea , Animais , Aspirina/metabolismo , Aspirina/farmacocinética , Inibidores da Agregação Plaquetária/metabolismo , Inibidores da Agregação Plaquetária/farmacocinética , Coelhos
2.
Med Tekh ; (3): 33-5, 2008.
Artigo em Russo | MEDLINE | ID: mdl-18688942

RESUMO

The goal of this work was to develop and test transdermal therapeutic systems for caffeine delivery. In vitro experiments showed that the rate of caffeine diffusion through untreated rabbit skin from a transdermal therapeutic systems based on polymer compound containing 50 mg medicine was 67.2 (9.1 microg/cm2h; for a system based on emulsion compound it was 173 (19 microg/cm2h. Methods for studying the caffeine release rate and quantitative measurement of caffeine content in the emulsion-based transdermal therapeutic system were developed. These methods are required to obtain data for standard drug documentation. The results of in vivo experiments in rabbits showed the absence of irritating effect of the emulsion-based transdermal therapeutic system. The obtained data on the specific efficiency of the transdermal therapeutic systems for caffeine delivery (50 mg) in healthy volunteers showed that this medicine could be used as a nonnarcotic psychoactivator for improving mental and physical activities and attention concentration.


Assuntos
Cafeína/administração & dosagem , Benzoato de Sódio/administração & dosagem , Administração Cutânea , Adulto , Animais , Cafeína/efeitos adversos , Sistemas de Liberação de Medicamentos , Emulsões , Humanos , Técnicas In Vitro , Masculino , Polímeros , Coelhos , Absorção Cutânea , Benzoato de Sódio/efeitos adversos
3.
Med Tekh ; (2): 21-4, 2003.
Artigo em Russo | MEDLINE | ID: mdl-12924217

RESUMO

A possibility is studied of the transdermal delivery of insulin by using a mixture of synthetic analogues of phosphoglycerides (SAP), as a potential activator of hormone diffusion, through the skin. Experimentally in vitro, it was proven that the diffusion of insulin through the skin of two types of transdermal therapeutic form (TTF)--matrix-type and matrix-hydrogel-type--is possible only in presence of activator SAP-M-99. The detected optimal composition of insulin matrix TTF with the area of 40 sq cm enabled a trandermal hormone diffusion speed of 0.26 UNITS/h, which is compatible with the secretion of insulin by the pancreas of an adult (0.25-1.5 UNITS/h). A change-over for the matrix-hydrogel system of insulin delivery based on a 40 sq cm collagenous sponge enabled to increase the insulin diffusion up to 0.54 UNITS/h.


Assuntos
Sistemas de Liberação de Medicamentos/métodos , Glicerofosfolipídeos/farmacocinética , Insulina/administração & dosagem , Pele/metabolismo , Adesivos , Adjuvantes Farmacêuticos , Administração Cutânea , Animais , Difusão , Estudos de Viabilidade , Glicerofosfolipídeos/síntese química , Hidrogéis , Insulina/farmacocinética , Coelhos , Absorção Cutânea , Suínos
5.
ASAIO Trans ; 36(3): M181-4, 1990.
Artigo em Inglês | MEDLINE | ID: mdl-2252653

RESUMO

This report summarizes 1) features of the local redistribution of calcium ions and formation of complexes with calcium (Ca) in the presence of polymer samples; 2) the adsorption of Ca ions and Ca containing complexes onto biomaterial surfaces; 3) the character and composition of Ca containing deposits; and 4) the role of cellular and humoral factors in calcification. All experiments were done with three types of medical grade polymer material (from USSR): silicone rubber (SR), polyurethane "Vitur" (PU), and polyethylene (PE). Biochemical, radioisotopic, SEM, and EDAX methods were used in in vitro and in vivo experiments. The diffusion chamber model was used in animal experiments. SR was shown to induce greater changes in complex formation processes and to adsorb more Ca containing complexes than PE or PU. In addition to the degree of SR calcification seen after 21 days, implantation accentuated these findings. The possibility of calcification of polymer materials without direct contact of material and cells was observed. Combining the in vitro and in vivo experimental data, the authors propose a hypothetical scheme of biomaterial calcification.


Assuntos
Materiais Biocompatíveis , Calcinose/sangue , Cálcio/sangue , Reação a Corpo Estranho/sangue , Adsorção , Animais , Humanos , Polietilenos , Politetrafluoretileno , Poliuretanos , Coelhos , Elastômeros de Silicone
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