Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Mucoadhesive patches containing 10mg miconazole nitrate were evaluated. The patches were prepared with ionic polymers, sodium carboxymethyl cellulose (SCMC) and chitosan, or non-ionic polymers, polyvinyl alcohol (PVA), hydroxyethyl cellulose (HEC) and hydroxypropylmethyl cellulose (HPMC). Convenient bioadhesion, acceptable elasticity, swelling and surface pH were obtained. Patches exhibited sustained release over more than 5h and the addition of polyvinyl pyrrolidone (PVP) generally enhanced the release rate. Optimum release behaviour was shown with patches containing 10% w/v PVA and 5% w/v PVP. Study of the in vivo release from this formulation revealed uniform and effective salivary levels with adequate comfort and compliance during at least 6h. On the contrary, in vivo release of the commercial oral gel product resulted in a burst and transient release of miconazole, which diminished sharply after the first hour of application. Storage of these patches for 6 months did not affect the elastic properties, however, enhanced release rates were observed due to marked changes in the crystal habit of the drug.

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0378-5173(03)00371-5DOI Listing

Publication Analysis

Top Keywords

miconazole nitrate
8
enhanced release
8
vivo release
8
release
7
patches
6
mucoadhesive buccal
4
buccal patches
4
patches miconazole
4
nitrate vitro/in
4
vitro/in vivo
4

Similar Publications

Background: Normal hydration of the canine epidermis is imperative for cutaneous homeostasis. Xerosis may be encountered in canine atopic dermatitis and is aggravated by topical antiseptics.

Hypothesis And Objectives: To evaluate the hydrating properties and the safety of a spray (Sensiderm spray; MP Labo) when applied after shampooing healthy dogs with a chlorhexidine 2%/miconazole 2% product.

View Article and Find Full Text PDF

During pregnancy there is an increased risk of vulvovaginal candidiasis that if left untreated is associated with pregnancy complications. First choice of treatment are over-the-counter azole antifungal drugs (AADs): miconazole, and clotrimazole, or prescription drug: fluconazole, which are suspected endocrine disruptive compounds. To investigate foetal exposure and endocrine disrupting effects of AADs on the human placenta, we added R-miconazole, S-miconazole, clotrimazole and fluconazole to the maternal reservoir of a dually recirculating ex vivo human term placental perfusion model.

View Article and Find Full Text PDF

Long-term antifungal drug-delivery denture materials with plasma-initiated surface functionalization.

Colloids Surf B Biointerfaces

December 2025

Chemistry Department, University of Massachusetts Lowell, One University Ave, Lowell, MA 01854-2874, USA. Electronic address:

Conventional polymethylmethacrylate (PMMA)-based denture materials are susceptible to colonization and biofilm-formation by Candida species, leading to Candida-associated denture stomatitis (CADS), a recurring fungal infection that affects a large patient population. In this report, we developed a two-step, plasma-initiated surface functionalization approach to covalently bond poly (methacrylic acid) (PMAA) onto denture resins. Various reaction conditions were investigated and the effects of PMAA grafting yields on the physical properties of the resulting denture materials were determined.

View Article and Find Full Text PDF

Background: Vulvovaginal candidiasis (VVC) is a common fungal infection primarily caused by Candida albicans. It is associated with significant morbidity, especially in recurrent cases. Antifungal resistance, particularly to azole drugs, poses a growing challenge in treatment.

View Article and Find Full Text PDF

Miconazole attenuates LPS-induced lung inflammation by modulating alveolar macrophage polarization via promoting lipid metabolic reprogramming.

Inflamm Res

August 2025

Perioperative and Systems Medicine Laboratory, Department of Pulmonology, Laboratory Animal Center, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, 310052, China.

Objective: Pulmonary inflammation is closely associated with macrophage polarization and lipid metabolic reprogramming. Miconazole (MCZ), traditionally used as an antifungal agent, exhibits emerging anti-inflammatory potential, yet its underlying mechanisms remain unclear.

Methods: A mouse model of lipopolysaccharide (LPS)-induced lung inflammation was employed to evaluate MCZ's anti-inflammatory efficacy.

View Article and Find Full Text PDF