Results 31 to 40 of about 37,692 (229)
Evaluation of Itraconazole and in Combination in the Treatment of Resistant and Recurrent Tinea Corporis and Cruris (Comparative Study) [PDF]
Background: One of the most prevalent dermatological disorders in the world is tinea infection. Itraconazole is still a crucial medication for treating and preventing fungal infections. Because of its wide range of action, terbinafine (TBF) is frequently
Mohammed Ewaiss +2 more
doaj +1 more source
Combining derivative and synchronous approaches for simultaneous spectrofluorimetric determination of terbinafine and itraconazole [PDF]
In this study, determination of terbinafine and itraconazole down to biological concentration level has been carried out. The determination is based on increasing the selectivity of the spectrofluorimetric technique by combining both derivative and ...
Heba Elmansi +3 more
doaj +1 more source
Scedosporium and Lomentospora infections in humans are generally chronic and stubborn. The use of azoles alone cannot usually inhibit the growth of these fungi.
Zikuo Wang +5 more
doaj +1 more source
Background: Few studies have examined the effect of seborrheic dermatitis (SD) and/or its consequent therapy on a patient’s quality of life. Itraconazole has been suggested as an effective therapy for severe SD but its impact on Quality of Life (QoL) in ...
Zaheer Abbas +2 more
doaj +1 more source
Bioavailability of single-dose SUBA-itraconazole compared to conventional itraconazole under fasted and fed conditions [PDF]
Conventional itraconazole (C-ITZ) suffers from absorption variability. SUBA-itraconazole (S-ITZ) is more bioavailable than C-ITZ at steady state in a fed condition, but there are no data comparing the two under a fasted state. An open-label, single-dose,
Rauseo, Adriana M +11 more
core +1 more source
Itraconazole and fluconazole have been reported to induce hepatotoxicity in patients. The present study was designed to investigate the role of cytochrome P450 inhibitors, SKF 525A, and curcumin pretreatment on the cytotoxicity of antifungal drugs ...
Nhareet Somchit +4 more
doaj +1 more source
Itraconazole is a triazole analogue with a broad spectrum of antifungal activity, which covers yeasts and moulds. It is active against dermatophytes, candidal and pityrosporum yeasts, as well as a number of fungi which cause subcutaneous and systemic infection. It is well absorbed and has significantly fewer side-effects than systemic imidazoles. It is
openaire +2 more sources
Yueyue Liu, Qian Zhang, Chao Lu, Wei Hu Department of Clinical Pharmacology, The Second Hospital of Anhui Medical University, Hefei, 230601, People’s Republic of ChinaCorrespondence: Chao Lu; Wei HuDepartment of Clinical Pharmacology, The Second ...
Liu Y, Hu W, Lu C, Zhang Q
core
Short-Course Itraconazole in the Treatment of Candida Vulvovaginitis: A Multicentre Canadian Study
OBJECTIVE: To determine the clinical and mycological effectiveness of oral itraconazole in the treatment of acute candida ...
Thomas W Austin +7 more
core +1 more source
This review critically evaluates clotrimazole as a potential antifungal for finfish aquaculture, highlighting strong mechanistic and in vitro efficacy against aquatic mycoses alongside major gaps in in vivo evidence, toxicokinetics, residue safety, and environmental risk, outlining priorities for responsible therapeutic development and regulatory ...
Arya Sen +2 more
wiley +1 more source

