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  • DEVELOPMENT & EVALUATION OF TRANSDERMAL DRUG DELIVERY

    ABOUT AUTHOR:
    Rakesh Kumar Sati
    M.Pharm D.I.T Faculty of Pharmacy
    Dehradun Uttarakhand
    rakeshsatiq.a@gmail.com

  • EXPERIMENTAL DESIGN

    ABOUT AUTHORS:
    *Rakesh Gupta, Hemant Kumar Sharma, Manvendra Jaiswal, Rajeev Sharma, Narendra Nyola, Dr. Rajesh Yadav
    Alwar Pharmacy College, M.I.A. Alwar,
    Rajasthan, India 301001
    rakeshapcpharma@gmail.com

  • FORMULATION AND EVALUATION OF QUETIAPINE FUMARATE SUSTAINED RELEASE MATRIX TABLET

    ABOUT AUTHORS:
    Pranita T. Gaikwad*, Reshma R.Patil, Mr M.M.Nitalikar, Dr.S.S.Patil, Dr.S.K.Mohite
    Rajarambapu college of pharmacy,
    kasegaon-415404. MH
    *pranitatgaikwad@gmail.com

  • THE ROLE OF SECONDARY MESSENGER SYSTEM IN SIGNAL TRANSDUCTION

    About Authors:
    Mr. Salahuddin Mohammed
    Associate Professor of Pharmacology, College of Health Sciences,
    Department of Pharmacy, Mizan Tepi University,
    Mizan Teferi, Ethiopia.
    salahuddin_pharma48@yahoo.com

  • FORMULATION AND EVALUATION OF ESOMEPRAZOLE MAGNESIUM DELAYED RELEASE TABLETS 40 MG

    ABOUT AUTHORS:
    *1MR.B.Ashok, 2Dr.K.S.Manjunatha Shetty, 3Dr. Manikanta kumar, Chandra Shekar
    1Master of Pharmacy in Pharmaceutics
    2Ph.D Professor and Principal
    3Ph.D, Associate Professor
    Jawaharlal Nehru Technological University, Hyderabad
    Srinivasa Pharmaceutical Institute And Center For Research Burugupally, Vikarabad, R.R Dist, A.P.
    ashok.belde@gmail.com

    ABSTRACT
    The present study was an attempt to formulate and evaluate enteric coated tablets for esomeprazole magnesium dihydrate. Different core tablets were prepared and formulation was selected for further enteric coating, based on the disintegration time. Seal coating was applied to achieve 3% weight gain. Enteric coating was carried out using different polymers like hydroxyl propyl methylcellulose phthalate to achieve 5% weight gain. Disintegration studies showed that the formulations failed in 0.1 N HCl media. Hence the quantity of enteric coating was increased to 8% w/w. In vitro analysis of the developed tablets was carried out. Results from disintegration time and dissolution rate studies indicate that all the esomeprazole enteric tablets prepared possess good integrity, desirable for enteric coated tablets.

  • TRANSDERMAL A NOVEL DRUG DELIVERY SYSTEM

    About Author:
    Dheeraj Fulara
    DIT Faculty of Pharmacy, Mussoorie Diversion Road, Dehradun 248009,
    Uttarakhand, India.
    fularadheerajmpharm@yahoo.com

  • LIPOSOMES AN OVERVIEW– A NOVEL TREND IN THE DRUG DELIVERY

    ABOUT AUTHORS:
    *Sambhara Gayatri Deepti1, Aruna Ragidi1, A.M.S.Sudhakar Babu1, P.Venkateswara Rao2
    1Department of Pharmaceutics
    2Department of Pharmaceutical Analysis
    A.M.Reddy Memorial college of Pharmacy, Narasaraopet, Guntur Dist., Andhra Pradesh, India.
    gayatri.dpt11@gmail.com

  • A REVIEW ON IMPLANTABLE DRUG DELIVERY SYSTEM

    ABOUT AUTHORS:
    Jyoti Malik
    Hindu College of Pharmacy,
    Sonepat, Haryana
    jyotimalik127@gmail.com

    ABSTRACT:
    There was a need for delivery systems that could maintain a steady release of drug to the specific site of action. Therefore, drug delivery systems were developed to optimize the  therapeutic properties of drug products and render them more safe, effective, and reliable. In comparison with many of the other drug delivery systems, implantable pumps and implants for variable rate delivery are at a crude stage of development. Although the typical implantable pump consists of different mechanisms to regulate drug delivery. The benefits most often provided by the dosage form are expected to be 1) Implantable devices allow site specific drug administration where the drug is needed most. Examples include implants used in the treatment of brain tumors or prostate cancer. This may also allow for significantly lower doses of the drug, which can minimize potential side effects. 2)Implantable devices allow for sustained releaseby the zero-order release rate of a therapeutic agent. The major advantages of these systems contain targeted local delivery of drugs at a constant rate, fewer drugs required to treat the disease state, minimization of probable side effects, and better efficacy of treatment. Due to the development of such sustained release formulations, it is now possible to administer unstable drugs once a week to once a year that in the past required frequent daily dosing.

  • A REVIEW ARTICLE ON TRANSDERMAL DRUG DELIVERY SYSTEM

    About Author:
    Mohit Dangwal
    DIT Faculty of Pharmacy
    Dehradun, Uttarakhand
    dangwal_mohit@yahoo.in

  • FORMULATION AND DEVELOPMENT OF VENLAFAXINE HYDROCHLORIDE EXTENDED RELEASE TABLET USING COMPRESSION COATING TECHNIQUE

    About Authors:
    K.Venkatakrishna
    Department of Pharmaceutics; Koringa college of pharmacy,
    Korangi (Andhra Pradesh) India.
    venky5019@gmail.com

    Abstract:
    Venlafaxine HCl is an anti depressent drug which is used in depreesion. It is available both as immediate release tablet as well as modified release product. The innovator modified release product available in international market is Effexor ER tablets. Effexor ER is based on erosion matrix system. The core tablet is coated with Ethyl Cellulose using PVP as a core former. This coating is solvent based coating. The aim of  present investigation was to prepare a ER tablet of Venlafaxine HCl  with similar dissolution profile matching to  Effexor ER  using  swelling  matrix system. The platform developed for this product was compression coating.  An immediate release  core tablet of 100mg  was prepared and it was compression coated using HPMC  matrix system. HPMC of three viscosity grades was selected and the concentration and the   viscosity grade were optimised. Similarity factor ( F2 values) with innovator product were calculated for in vitro dissolution profile.  The  rank order correlation for similarity factor was as under HPMC K15M 15% > HPMC K100M 15% > HPMC k15M 35% > HPMC k100M 35% > HPMCK 4M 15% > HPMC k45 45%. In this review, current and recent developments of venlafaxine hydrochloride extended release products are discussed.

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