Formulation and evaluation of itraconazole gel

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  • Preformulation studies Selection and collection of raw materials
  • 89 IF6 6
  • 3 IF6 95
  • The main
  • The preparation of niosomes
  • FORMULATION AND EVALUATION OF ITRACONAZOLE OPTHALMIC IN SITU GELS M
  • 67 % for ITZG-2
  • Article
  • 57, 19
  • 20
  • 78% in 72 hrs, which contains carbopol 934p
  • The gel formulation had a release rate of 69
  • 88 Formulation Drug content (%) IF1 98

    Pharmacy, Department of Pharmaceutics, Sri Padmavathi School of Pharmacy, Jawaharlal Nehru Technological

    Formulation and Evaluation of Itraconazole Novel Nanosuspension-Based In Situ Gelling System for Vaginal Candidiasis Using 2 Table 7 Results of ANOVA study for

    Arora View Show The present research work deals with the formulation and evaluation of in-situ gelling system based on sol-to-gel transition for ophthalmic delivery of an antibacterial agent

    Itraconazole niosomal gel was prepared using Carbopol 940, glycerol, triethanolamine and distilled water

    Topical and Cosmetic Sci

    Evaluation of niosomal gel was determined by physical appearance, pH

    It was concluded that formulation F3 was the best formulation among this formulation of Itraconazole and should be further developed for scale-up to industrial production

    edu Itraconazole is a broad spectrum Imidazole derivative useful in the treatment of superfacial and systemic fungal infection

    Results indicate that F exhibits maximum antifungal activity after 24 h

    Purpose This study aimed to produce lipid complex-ITR (CL-ITR) to enhance the

    22159/ijcpr

    & Res

    Liquid crystal systems are used to tailor drug delivery from topical delivery system

    Formulation and Evaluation of Itraconazole Niosomal Gel

    Liquid crystalline gel formulations were prepared by using glyceryl mono-oleate GMO, water and other

    No

    However, some studies have The high value of firmness indicates that Based Gel the formulation will be adhered to the skin appreciably The pH of the microemulsion based hydrogels was and for longer period which would help to deliver the be- tween 5

    This slow release may be due to release from nanovesicles and diffusion of the drug through the network structures of the itraconazole-loaded nanosuspension, and a 24 complete factorial experimental design was used

    The present study was to formulate and evaluate the Itraconazole niosomal gel using surfactant span 40, 60 and tween 60 for the preparation of niosomes

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  • Formulation and evaluation of itraconazole gel
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