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In-vitro drug diffusion

DESIGN AND IN VITRO EVALUATION OF TENOXICAM NANOGEL CONTAINING NOVEON POLYMER

DESIGN AND IN VITRO EVALUATION OF TENOXICAM NANOGEL CONTAINING NOVEON POLYMER

... high drug loading capacity, biocompatibility, and biodegradability which are the key points to design a drug delivery system ...nanogel drug delivery system concerning drug loading and ...

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Formulation and Evaluation of Tacrolimus Transdermal Gel

Formulation and Evaluation of Tacrolimus Transdermal Gel

... anti-psoriasis drug, to circumvent the first pass effect and to improve its bioavailability with reduction in dosing frequency and dose related side ...pH, drug Content uniformity, in-vitro ...

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DESIGN OF TRAMADOL HYDROCHLORIDE LOADED SOLID LIPID NANOPARTICLES BASED GELS FOR PAIN MANAGEMENT

DESIGN OF TRAMADOL HYDROCHLORIDE LOADED SOLID LIPID NANOPARTICLES BASED GELS FOR PAIN MANAGEMENT

... in vitro drug diffusion profile and evaluate the developed formulations for topical application for pain ...method. Drug release followed diffusion controlled kinetics and released the ...

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RESEARCH ON FORMULATION AND EVALUATION OF INSITU MUCOADHESIVE NASAL GELS OF METOCLOPRAMIDE HYDROCHLORIDE

RESEARCH ON FORMULATION AND EVALUATION OF INSITU MUCOADHESIVE NASAL GELS OF METOCLOPRAMIDE HYDROCHLORIDE

... of drug formulation in the nasal cavity is of utmost importance for intranasal drug ...antiemetic drug, Metoclopramide ...and drug release enhancement were modulated via the use of sodium ...

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Volume 3 | Issue 3 - 2013

Volume 3 | Issue 3 - 2013

... anti-inflammatory drug, to circumvent the first pass effect and to improve its bioavailability with reduction in dosing frequency and dose related side ...pH, drug Content uniformity, in-vitro ...

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PROLONG RELEASE BIOADHESIVE VAGINAL FILM OF ANTI HIV DRUG (ZIDOVUDINE): FORMULATION AND IN  VITRO EVALUATION

PROLONG RELEASE BIOADHESIVE VAGINAL FILM OF ANTI HIV DRUG (ZIDOVUDINE): FORMULATION AND IN VITRO EVALUATION

... In vitro drug release and release kinetics of VFs: In vitro drug diffusion studies were carried out by using ...The drug was estimated by using UV-Visible spectrophotometer at ...

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Formulation and evaluation of Lornoxicam loaded Lyotropic liquid crystalline gel

Formulation and evaluation of Lornoxicam loaded Lyotropic liquid crystalline gel

... in vitro drug release of the Lornoxicam loaded lyotropic liquid crystalline gel was performed to investigate the amount of drug released from a ...

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 FORMULATION AND EVALUATION OF EMULGEL OF FLURBIPROFEN

 FORMULATION AND EVALUATION OF EMULGEL OF FLURBIPROFEN

... Topical drug delivery has been used for the treatment of local skin ...the drug offer the potential advantages of delivering the drug directly to the site of action and secondly delivering the ...

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DESIGN OF OCULAR CONTROLLED RELEASE OCUSERTS OF BRINZOLAMIDE

DESIGN OF OCULAR CONTROLLED RELEASE OCUSERTS OF BRINZOLAMIDE

... release drug delivery system like ocuserts of Brinzolamide, an anti-glaucoma ...as drug reservoir membrane and controlled release polymers like Eudragit as the rate limiting ...of drug content, in ...

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Ion-activated In Situ Gelling Ophthalmic Delivery Systems of Azithromycin

Ion-activated In Situ Gelling Ophthalmic Delivery Systems of Azithromycin

... in vitro drug release studies by diffusion through dialysis membrane on the three formulations HLP3, HKP3 and CP2 are given in the ...of drug diffusion correlates well with the gel ...

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Journal of Applied Pharmaceutical Science

Journal of Applied Pharmaceutical Science

... anti-inflammatory drug is widely used in the treatment of rheumatoid arthritis, ankylosing spondulytis and ...potential drug for prevention and treatment of colorectal ...this drug is its low ...

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WOUND- HEALING ACTIVITY OF A PREPARED LONG ACTING GEL  LOADED WITH CIPROFLOXACILIIN HCL MICROSPHERES  IN ALBINO RATS

WOUND- HEALING ACTIVITY OF A PREPARED LONG ACTING GEL LOADED WITH CIPROFLOXACILIIN HCL MICROSPHERES IN ALBINO RATS

... The drug-loaded microspheres were prepared by solvent evaporation technique 1, 2 and loaded into 1%, 2% and 3% carbopol gel ...for drug content and viscosity .The in vitro diffusion studies ...

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SYNTHESIS, ANTIBACTERIAL ACTIVITY AND MOLECULAR PROPERTIES PREDICTION OF SOME PYRIDAZIN 3 ONE DERIVATIVES

SYNTHESIS, ANTIBACTERIAL ACTIVITY AND MOLECULAR PROPERTIES PREDICTION OF SOME PYRIDAZIN 3 ONE DERIVATIVES

... Likeness: Drug likeliness is a qualitative means of analysis to check whether the given molecule is a drug or not and it is defined as a complex balance of various molecular properties and structural ...

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... In-vitro drug release study: The in-vitro diffusion studies were carried out using Franz diffusion cell apparatus and semi-permeable cellophane ...Franz diffusion cell with a ...

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Papaverine hydrochloride containing nanostructured lyotropic liquid crystal formulation as a potential drug delivery system for the treatment of erectile dysfunction

Papaverine hydrochloride containing nanostructured lyotropic liquid crystal formulation as a potential drug delivery system for the treatment of erectile dysfunction

... Franz diffusion cell (Hanson Microette TM Topical & Transdermal Diffusion Cell System, Hanson Research Corporation, Chatsworth, CA USA) was used to model the drug liberation from the LLCs and ...

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Design and evaluation of matrix type and membrane controlled transdermal delivery systems of nicotine suitable for use in smoking cessation

Design and evaluation of matrix type and membrane controlled transdermal delivery systems of nicotine suitable for use in smoking cessation

... The drug content was found to be uniform in the patches. In vitro release studies of transdermal patches showed a biphasic release pattern, with diffusion as the dominating mechanism of drug ...

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FORMULATION DEVELOPMENT AND EVALUATION OF CLOPIDOGREL BISULFATE TRANSDERMAL PATCHES

FORMULATION DEVELOPMENT AND EVALUATION OF CLOPIDOGREL BISULFATE TRANSDERMAL PATCHES

... a drug used in inhibiting the platelet aggregation and also used in the treatment of cardiovascular ...of drug is excreted in urine and 40% in feces. The plasma half life of drug is about 8 hours ...

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LYOTROPIC LIQUID CRYSTALLINE SYSTEM FOR EFFECTIVE TOPICAL DELIVERY OF TOLNAFTATE

LYOTROPIC LIQUID CRYSTALLINE SYSTEM FOR EFFECTIVE TOPICAL DELIVERY OF TOLNAFTATE

... dermal drug delivery system. The liquid crystalline system enhance the diffusion of water insoluble drug Tolnaftate through the skin for effective ...the drug in liquid crystal increased its ...

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Enhanced Topical Formulation of Minoxidil Gel

Enhanced Topical Formulation of Minoxidil Gel

... of drug release ...in drug release rate is observed. The drug release from the Natrosol, Carbopol 974 and HPMC K100 formulations were controlled by polymer swelling and diffusion and followed ...

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FORMULATION AND EVALUATION OF FLUCONAZOLE OCULAR INSERTS

FORMULATION AND EVALUATION OF FLUCONAZOLE OCULAR INSERTS

... variation, drug content, surface pH, swelling index, folding endurance, percentage moisture loss, and moisture absorption ...In vitro diffusion studies of formulated ocular inserts were performed by ...

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