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1.
Pharmazie ; 62(11): 858-63, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18065103

RESUMO

Halofantrine (HF) is a poorly water-soluble antimalarial drug with low bioavailability. Complex formation of HF.HCl and 2-hydroxypropyl-beta-cyclodextrin (HP-beta-CD) in aqueous solution and in solid state as well as the possibility of improving the solubility and dissolution rate of the drug though complexation with the cyclodextrin were investigated. Phase-solubility profile indicated that the solubility of the drug was significantly increased in the presence of HP-beta-CD and was classified as AL-type, indicating 1:1 stoichiometric inclusion complexes and an apparent stability constant value of 2300 M(-1). Solid inclusion complexes of HF, HCl and the cyclodextrin at 1:1 molar ratios were prepared by physical mixture, kneading, co-evaporation and freeze-drying methods and characterized by X-ray diffraction and Infra-red spectroscopy. The solubility and dissolution rates of HF.HCl from the complexes were determined and found to be dependent on the preparation method of the complexes. Dissolution profile of the drug was markedly enhanced by complex formation with the cyclodextrin and the product prepared by the freeze-drying method exhibited the most superior dissolution properties compared to the other methods used in this study. The results suggest that the complexation of HF.HCl with HP-beta-CD could improve therapeutic efficacy of the drug though enhanced absorption expected from increased drug dissolution.


Assuntos
Fenantrenos/química , beta-Ciclodextrinas/química , 2-Hidroxipropil-beta-Ciclodextrina , Cristalografia por Raios X , Liofilização , Indicadores e Reagentes , Cinética , Solubilidade , Espectrofotometria Infravermelho , Água/química
2.
Phytother Res ; 17(5): 555-7, 2003 May.
Artigo em Inglês | MEDLINE | ID: mdl-12748998

RESUMO

In an open non-comparative study to evaluate the efficacy and safety of Acalypha wilkesiana ointment in superficial fungal skin diseases, 32 Nigerian patients with clinical and mycological evidence of superficial mycoses were recruited. Twelve patients defaulted and were lost to follow up, while one patient withdrew because of intolerable excoriation at the site of the lesion. Of the 19 patients that completed the trial, clinical cure was achieved in 73.3% of the patients. The ointment was very efficacious in the treatment of Tinea pedis, Pityriasis versicolor and Candida intetrigo where the cure rate was 100% in each condition. It is recommended that Acalypha ointment can be used for the treatment of these superficial mycoses.


Assuntos
Dermatomicoses/tratamento farmacológico , Euphorbiaceae , Pomadas/uso terapêutico , Fitoterapia , Extratos Vegetais/uso terapêutico , Candidíase/tratamento farmacológico , Feminino , Humanos , Kwashiorkor/tratamento farmacológico , Masculino , Nigéria , Folhas de Planta/química , Tinha dos Pés/tratamento farmacológico , Tinha Versicolor/tratamento farmacológico , Resultado do Tratamento
3.
Int J Pharm ; 237(1-2): 241-9, 2002 Apr 26.
Artigo em Inglês | MEDLINE | ID: mdl-11955821

RESUMO

The required HLB values of eucalyptus, lippia and peppermint essential oils were determined using droplet size analysis and turbidimetric method on emulsions prepared with emulsifier blends of varying HLB values. The percentage increase in mean droplet diameter and the degree of dispersion of droplet sizes were determined before and after centrifugation of the emulsions. The HLB value of the emulsion with the least dispersion ratio or the least percentage increase in mean droplet diameter was taken as the required HLB of the respective essential oil. The turbidimetric method was validated by the existence of correlation (r=-0.958) between the mean droplet diameter and the turbidity of the emulsions. The turbidity curve went through a maximum at the HLB value where the mean droplet diameter was least. Based on these methods, the required HLB values of eucalyptus, lippia and peppermint oils were determined as 9.8, 12.1 and 12.3, respectively (P<0.05). Liquid paraffin was used as a reference standard and its required HLB fell within literature value.


Assuntos
Óleos Voláteis/química , Centrifugação , Emulsões , Microscopia , Nefelometria e Turbidimetria
4.
Afr J Med Med Sci ; 30(4): 275-80, 2001 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-14510103

RESUMO

Three leading and competitive commercial products of paracetamol tablets coded as brands A, B and C (A, being the innovator product) in the country were evaluated for their in vitro properties and in vivo comparative bioavailability. The studies included chemical equivalence, hardness, disintegration time, dissolution rate and systemic availability among eight healthy volunteers. The disintegration times were 2.1 min for brand A, 5.7 min for brand B and 36.2 min for brand C. The dissolution rate (T70) were 33.0 min, 74.5 min and 56.5 min for brands A, B and C, respectively. While brand A passed all the in vitro tests as specified in the official monograph, brand B failed only the dissolution rate test and brand C failed both the disintegration and dissolution tests. These significant differences observed among the products after in vitro tests were not reflected in the in vivo availability. While the absorption rate (indicated by tmax) of brand C was significantly faster (i.e. shorter) than those of Brands A and B, the extent of absorption (indicated by AUC) was comparable among the three brands. The relative bioavailabilities (with respect to brand A) were 92 and 91% for brands B and C, respectively indicating that the products were bioequivalent. Comparison of the in vitro and in vivo data suggest that the systemic absorption of paracetamol may not be dissolution--rate limited and that using in vitro dissolution rate studies alone to establish bioequivalency of paracetamol tablets should be done with caution.


Assuntos
Acetaminofen/química , Acetaminofen/farmacocinética , Analgésicos não Narcóticos/química , Analgésicos não Narcóticos/farmacocinética , Adulto , Disponibilidade Biológica , Humanos , Masculino , Solubilidade , Comprimidos
5.
J Ethnopharmacol ; 72(1-2): 305-11, 2000 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10967487

RESUMO

The essential oil from the leaves of Lippia multiflora Moldenke (Verbenaceae) was tested for its pediculocidal and scabicidal activites against bodylice, headlice and scabies' mites. The 'knockdown' times obtained for bodylice and headlice using lippia oil preparations were comparatively shorter than those obtained using benzyl benzoate and Delvap Super, a brand of dichlorvos. The lethal effect of the lippia oil on headlice was increased when applied in an enclosed system that prevented volatilization of the oil while allowing maximum contact of the vapour with the headlice. A 20% v/v preparation of lippia oil applied to scabietic subjects for 5 consecutive days gave 100% cure compared with 87.5% cure obtained for benzyl benzoate preparation of the same concentration. The GC-MS analysis of oil revealed, among others, the presence of terpineol, alpha- and beta-pinene which are known to be lethal to body and headlice.


Assuntos
Infestações por Piolhos/tratamento farmacológico , Óleos Voláteis/uso terapêutico , Óleos de Plantas/uso terapêutico , Plantas Medicinais/química , Escabiose/tratamento farmacológico , Adulto , Idoso , Animais , Cromatografia Gasosa , Método Duplo-Cego , Cromatografia Gasosa-Espectrometria de Massas , Humanos , Masculino , Pessoa de Meia-Idade , Nigéria , Óleos Voláteis/química , Pediculus , Óleos de Plantas/química
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