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Oral candidiasis is an opportunistic infection that affects mainly individuals with weakened immune system. Devices used in the oral area to treat this condition include buccal films, which present advantages over both oral tablets and gels. Since candidiasis causes pain, burning, and itching, the purpose of this work was to develop buccal films loaded with both lidocaine (anesthetic) and miconazole nitrate (MN, antifungal) to treat this pathology topically. MN was loaded in microparticles based on different natural polymers, and then, these microparticles were loaded in hydroxypropyl methylcellulose-gelatin-based films containing lidocaine. All developed films showed adequate adhesiveness and thickness. DSC and XRD tests suggested that the drugs were in an amorphous state in the therapeutic systems. Microparticles based on chitosan-alginate showed the highest MN encapsulation. Among the films, those containing the mentioned microparticles presented the highest tensile strength and the lowest elongation at break, possibly due to the strong interactions between both polymers. These films allowed a fast release of lidocaine and a controlled release of MN. Due to the latter, these systems showed antifungal activity for 24 h. Therefore, the treatment of oropharyngeal candidiasis with these films could reduce the number of daily applications with respect to conventional treatments.
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http://dx.doi.org/10.3390/ma16093586 | DOI Listing |
Vet Dermatol
September 2025
Clinic of Medicine, Faculty of Veterinary Science, University of Thessaly, Karditsa, Greece.
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.
Pharmacol Res
August 2025
Toxicology and Drug Metabolism Group, Department of Pharmacy, University of Copenhagen, Copenhagen, Denmark.
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 PDFColloids Surf B Biointerfaces
August 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 PDFBMC Microbiol
August 2025
Centre for Biotechnology, Siksha 'O' Anusandhan (Deemed to be University), Kalinganagar, Bhubaneswar, Odisha, 751003, India.
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 PDFInflamm 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.