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1.
Eur Psychiatry ; 17(8): 425-33, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12504258

RESUMO

In the case of a first episode of psychosis among members of different associations of families of mentally ill people, little is known about their priorities and how satisfied they are with the help provided to them. A survey was conducted in five European family associations. Respondents emphasized the need for early (ambulant) intervention through outreach with very practical goals directed at creating stability and social functioning. About one-third of the respondents are unsatisfied or very unsatisfied. The highest percentage of unsatisfied respondents was in the following five areas of care: advice on how to handle specific problems; help with preserving or regaining social functioning; help with regaining structure and routine; information; prompt assistance preferably in patients own environment. The agreement of these findings with findings from earlier studies underlines the importance of suggesting specific changes in the delivery of care.


Assuntos
Serviços Comunitários de Saúde Mental/provisão & distribuição , Saúde da Família , Prioridades em Saúde , Necessidades e Demandas de Serviços de Saúde , Satisfação do Paciente/estatística & dados numéricos , Transtornos Psicóticos/terapia , Adulto , Áustria/epidemiologia , Serviços Comunitários de Saúde Mental/economia , Custos de Cuidados de Saúde , Humanos , Irlanda/epidemiologia , Masculino , Pessoa de Meia-Idade , Transtornos Psicóticos/economia , Transtornos Psicóticos/epidemiologia , Escócia/epidemiologia , Espanha/epidemiologia , Inquéritos e Questionários , Suécia/epidemiologia , Fatores de Tempo
2.
Drug Deliv ; 9(1): 55-62, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-11839209

RESUMO

Bacopasaponin C, an indigenous glycoside, was isolated from Indian medicinal plant Bacopa monniera (b. brahmi) and was tested for antileishmanial properties both in free and in various delivery modes, e.g., niosomes, microspheres, and nanoparticles that are used now as alternatives to more commonly used liposomes. The different vesicles were prepared by published protocols. The percent intercalation of Bacopasaponin C in liposomes, niosomes, and micropspheres determined at its absorption maximal (lambda(max) = 238 nm, epsilon = 8.6 x 10(3) M(-1) x cm(-1)) was found to be 30; for nanoparticles it was 50. At equivalent dose of 1.75 mg/kg body weight, every third day for a total of 6 doses in 15 days, Bacopasaponin C in all the vesicular forms was found to be very active. An inverse linear relationship between the efficacy and the size of the vesicles was established. As analyzed from tissue histology, blood pathology, and specific tests related to normal liver and kidney functions, Bacopasaponin C in each of the four vesicular forms was found to be without any side effects. Thus, because of its indigenous origin and non-toxic nature, Bacopasaponin C could very well be considered for application in the clinic through these alternative delivery modes.


Assuntos
Antiprotozoários/administração & dosagem , Antiprotozoários/farmacologia , Glicosídeos/administração & dosagem , Glicosídeos/farmacologia , Leishmania donovani/efeitos dos fármacos , Triterpenos , Animais , Antiprotozoários/toxicidade , Cricetinae , Portadores de Fármacos , Glicosídeos/toxicidade , Técnicas In Vitro , Lipossomos , Fígado/efeitos dos fármacos , Macrófagos Peritoneais/efeitos dos fármacos , Mesocricetus , Camundongos , Camundongos Endogâmicos BALB C , Baço/parasitologia
3.
Indian J Biochem Biophys ; 36(4): 248-51, 1999 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10650726

RESUMO

The leishmanicidal property of piperine intercalated in liposomes and in mannose-coated liposomes was tested in experimental visceral leishmaniasis in hamsters. Mannose-coated liposomal piperine eliminated intracellular amastigotes of Leishmania donovani in splenic macrophages much more efficiently than did the liposomal piperine or free piperine. At a dose equivalent to 6 mg/kg body wt every 4th day for a total of 4 doses in 12 days, the mannose-coated liposomal piperine was found to reduce spleen parasite load to the extent of 90% in comparison to that achieved by liposomal piperine (77%) or free piperine (29%). Histological examination of spleen and liver function tests showed that the toxicity of piperine was reduced when mannosylated liposomal piperine was administered.


Assuntos
Alcaloides , Antiprotozoários/administração & dosagem , Leishmaniose Visceral/tratamento farmacológico , Piperidinas/administração & dosagem , Animais , Antiprotozoários/uso terapêutico , Benzodioxóis , Cricetinae , Portadores de Fármacos , Leishmaniose Visceral/fisiopatologia , Lipossomos , Testes de Função Hepática , Macrófagos/parasitologia , Manose/administração & dosagem , Mesocricetus , Piperidinas/uso terapêutico , Alcamidas Poli-Insaturadas , Baço/parasitologia , Baço/fisiopatologia
4.
Indian J Exp Biol ; 37(9): 871-5, 1999 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10687281

RESUMO

Studies have been performed to assess the possibility of using small unilamellar liposomes as therapeutic carriers to the brain of hypertensive rats. Rats were made temporal hypertensive by the infusion of angiotensin II (AII; 15 micrograms in 1 ml) through their right common carotid artery. Another control group was infused with physiological saline. Free 125iodine-BSA (125I-BSA) and 125I-BSA encapsulated liposomes (average diameter approximately equal to 100 nm) were injected in the tail vein 2 min after the infusion of AII or saline. Plasma radioactivity was monitored at different times up to 15 min when the cerebral uptake of 125I-BSA was determined. While a little variation in plasma clearance pattern of liposomes in hypertensive and control group was noticed, the uptake by cerebral tissues was markedly higher in hypertensive group. Analysis of pharmacokinetic parameters in relation to cerebral uptake indicated AII induced a short term opening of the blood-brain barrier (BBB) resulting in an increased cerebral uptake. Positively charged liposomes was found to be most effective in hypertensive state.


Assuntos
Angiotensina II/farmacologia , Encéfalo/efeitos dos fármacos , Angiotensina II/farmacocinética , Angiotensina II/uso terapêutico , Animais , Área Sob a Curva , Barreira Hematoencefálica , Encéfalo/metabolismo , Modelos Animais de Doenças , Portadores de Fármacos , Hipertensão/tratamento farmacológico , Lipossomos , Ratos
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