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1.
Indian J Pharmacol ; 48(5): 531-536, 2016.
Article in English | MEDLINE | ID: mdl-27721539

ABSTRACT

OBJECTIVES: The aim of this study was to investigate the antipsoriatic activity of ethanolic extract of Woodfordia fruticosa flowers (EEWF) using a novel in vivo screening model. MATERIALS AND METHODS: For induction of psoriasis, 0.1 ml of prepared complete Freund's adjuvant (CFA) and formaldehyde mixture (1:10 ratio) was topically applied for 7 days on the dorsum surface of the skin of Swiss albino mice. Psoriasis severity index (PSI) was evaluated by phenotypic (redness, erythema, and scales) and histological features (epidermal thickness). Therapeutic effect of 0.05% and 0.1% (w/w) ointments of EEWF was evaluated after the induction of psoriasis. Ointments of EEWF flowers were applied once daily for 3 weeks, and antipsoriatic activity was evaluated by scoring the PSI and histological examination. RESULTS: We observed the phenotypic and histological features and found a progressive reduction (P < 0.05) in the severity of psoriatic lesions (redness, erythema, and scales) from day 7 to 21st day and decreased epidermal thickness in animals treated with 0.05% and 0.1% (w/w) ointments of EEWF. CONCLUSIONS: The results showed that 0.05% and 0.1% (w/w) ointments of EEWF have dose-dependent beneficial effects in CFA and formaldehyde-induced psoriasis. The present investigation revealed that W. fruticosa flowers possess potent antipsoriatic activity and can be used for psoriasis treatment.


Subject(s)
Dermatologic Agents/therapeutic use , Disease Models, Animal , Plant Extracts/therapeutic use , Psoriasis/drug therapy , Woodfordia , Animals , Dermatologic Agents/chemistry , Dermatologic Agents/toxicity , Ethanol , Female , Flavonoids/analysis , Flowers/chemistry , Formaldehyde , Freund's Adjuvant , Male , Mice , Phenols/analysis , Phytotherapy , Plant Extracts/chemistry , Plant Extracts/toxicity , Psoriasis/chemically induced , Psoriasis/pathology , Skin/drug effects , Skin/pathology , Solvents , Toxicity Tests, Acute , Woodfordia/chemistry
2.
J Pharm (Cairo) ; 2016: 9249040, 2016.
Article in English | MEDLINE | ID: mdl-27018126

ABSTRACT

Objectives. The present study was aimed at investigating the wound healing effect of ethanolic extract of Cestrum nocturnum (L.) leaves (EECN) using excision and incision wound model. Methods. Wistar albino rats were divided into five groups each consisting of six animals; group I (left untreated) considered as control, group II (ointment base treated) considered as negative control, group III treated with 5% (w/w) povidone iodine ointment (Intadine USP), which served as standard, group IV treated with EECN 2% (w/w) ointment, and group V treated with EECN 5% (w/w) ointment were considered as test groups. All the treatments were given once daily. The wound healing effect was assessed by percentage wound contraction, epithelialization period, and histoarchitecture studies in excision wound model while breaking strength and hydroxyproline content in the incision wound model. Result. Different concentration of EECN (2% and 5% w/w) ointment promoted the wound healing activity significantly in both the models studied. The high rate of wound contraction (P < 0.001), decrease in the period for epithelialization (P < 0.01), high skin breaking strength (P < 0.001), and elevated hydroxyproline content were observed in animal treated with EECN ointments when compared to the control and negative control group of animals. Histopathological studies of the EECN ointments treated groups also revealed the effectiveness in improved wound healing. Conclusions. Ethanolic extract of Cestrum nocturnum (EECN) leaves possesses a concentration dependent wound healing effect.

3.
Eur J Med Chem ; 45(7): 2938-42, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20413186

ABSTRACT

As benzothiazole has proven to be good antimicrobial agent, a novel series of Schiff bases of benzothiazole derivatives were synthesized. Thus condensation of 5-[2-(1,3-benzothiazol-2-yl-amino) ethyl]-4-amino-3-mercapto-(4H)-1,2,4-triazole 5 with appropriate aromatic aldehydes afforded 5-[2-(1,3-benzothiazol-2-yl-amino)ethyl]-4-(arylideneamino)-3-mercapto-(4H)-1,2,4-triazoles 6a-g. Structures of the synthesized compounds were elucidated on the basis of elemental analyses and spectral data. All the synthesized compounds were screened for their antimicrobial activity.


Subject(s)
Anti-Infective Agents/chemical synthesis , Anti-Infective Agents/pharmacology , Benzothiazoles/chemical synthesis , Benzothiazoles/pharmacology , Anti-Infective Agents/chemistry , Azo Compounds/chemistry , Bacteria/drug effects , Benzothiazoles/chemistry , Fungi/drug effects , Thiosemicarbazones/chemistry
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