A topical microemulsion (ME)-based hydrogel was developed to enhance permeation of an antifungal drug, liranaftate (LRFE) for effective eradication of cutaneous fungal infection. Pseudo-ternary phase diagrams were used to determine the existence of MEs region. ME formulations were prepared with Di-isopropyl adaptate, Cremophore-EL, Ethanol and distilled water. Xanthan Gum (1.5% w/w) was used for preparation of hydrogel of LRFE microemulsion (HLM) and characterized. The in-vitro and ex-vivo evaluation of prepared HLM and saturated drug solution were compared. The viscosity, average droplet size and pH of HLM were 142.30±0.42 to 165.15±0.21Pas, 52.53-93.40nm and 6.6-7.1, respectively. Permeation rate of LRFE from optimized formulation (HLM-3), composed with Di-isopropyl adaptate (4.5% w/w), Cremophor-EL (30% w/w), Ethanol (10% w/w) and water (52% w/w) was observed higher in compare with other HLMs and saturated drug solution. HLM-3 was stable, six times higher drug deposition capacity in skin than saturated drug solution and did not caused any erythema based on skin sensitivity study on rat. The average zone of inhibition of HLM-3 (25.52±0.26mm) was higher in compare with saturated drug solution (13.44±0.40mm) against Candida albicans.
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http://dx.doi.org/10.1016/j.ijbiomac.2017.10.039 | DOI Listing |
Drug Dev Ind Pharm
January 2025
Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology (CHARUSAT), Changa - 388421, Anand, Gujarat, India.
Background: Tavaborole (TAV), a benzoxaborole derivative, is an FDA-approved antifungal agent for treating onychomycosis, a common and persistent fungal infection of the toenails.
Objective: This study aimed to develop a robust stability-indicating HPTLC method to determine TAV in nanostructured lipid carriers (NLC) using a comprehensive approach that includes risk assessment, and Analytical Quality by Design.
Methods: The critical method parameters influencing the HPTLC results were screened using a Placket-Burman screening design followed by its optimization using a central composite optimization design.
Elife
January 2025
State Key Laboratory of Biocontrol, School of Life Sciences, Guangdong Province Key Laboratory for Pharmaceutical Functional Genes, Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), Sun Yat-sen University, Guangzhou, China.
Non-inheritable antibiotic or phenotypic resistance ensures bacterial survival during antibiotic treatment. However, exogenous factors promoting phenotypic resistance are poorly defined. Here, we demonstrate that are recalcitrant to killing by a broad spectrum of antibiotics under high magnesium.
View Article and Find Full Text PDFFront Immunol
January 2025
University of Michigan, Department of Internal Medicine, Ann Arbor, MI, United States.
Introduction: Despite progress in systemic lupus erythematosus (SLE) treatment, challenges persist in medication adherence due to side effects and costs. Precision nutrition, particularly adjusting fatty acid intake, offers a cost-effective strategy for enhancing SLE management. Prior research, including our own, indicates that increased consumption of omega-3 polyunsaturated fatty acids (PUFAs) correlates with improved outcomes in SLE patients.
View Article and Find Full Text PDFTheranostics
January 2025
College of Pharmacy, Seoul National University, Seoul 08826, South Korea.
Hypoxia is a major obstacle in the treatment of solid tumors because it causes immune escape and therapeutic resistance. Drug penetration into the hypoxic regions of tumor microenvironment (TME) is extremely limited. This study proposes using the unidirectional fluid flow property of low-intensity pulsed ultrasound (LIPUS) to overcome drug penetration limitations in the TME.
View Article and Find Full Text PDFSci Rep
December 2024
Division of Musculoskeletal and Dermatological Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester and Northern Care Alliance NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, M13 9PT, UK.
Calcinosis cutis affects 20-40% of patients with systemic sclerosis. This study tests the hypothesis that calcium-chelating polycarboxylic acids can induce calcium dissolution without skin toxicity or irritancy. We compared citric acid (CA) and ethylenediaminetetraacetic acid (EDTA) to sodium thiosulfate (STS) for their ability to chelate calcium in vitro using a pharmaceutical dissolution model of calcinosis (hydroxyapatite (HAp) tablet), prior to evaluation of toxicity and irritancy in 2D in vitro skin models.
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