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  • ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS): A REVIEW

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    ABOUT AUTHOR
    Dr. (Mrs.) Anita Singh

    Department of Home Science,
    Kr. R.C.M. P.G College Mainpuri, U.P, India
    dranitasinghkrcm@gmail.com

    ABSTRACT
    Human immunodeficiency virus (HIV) is a lent virus (slowly-replicating retrovirus) that causes acquired immunodeficiency syndrome (AIDs). Infection with HIV occurs by the transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk. Within these bodily fluids, HIV is present as both free virus particles and virus within infected immune cells. HIV enters macrophages and CD4+ T cells by the adsorption of glycoproteins on its surface to receptors on the target cell followed by fusion of the viral envelope with the cell membrane and the release of the HIV capsid into the cell. There is no cure for HIV/AIDS, but a variety of drugs can be used in combination to control the virus.

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  • RECENT INDUSTRIAL DEVELOPMENT IN ORAL THIN FILM TECHNOLOGY: AN OVERVIEW

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    ABOUT AUTHORS
    Kh. Hussan Reza 1*, Pranabesh Chakraborty2
    1 Department of Pharmacy, Bengal School of Technology, Sugandha, Hooghly, West Bengal
    2 Director, Department of Pharmacy, Bengal School of Technology, Sugandha, Hooghly, West Bengal
    *hassan23pharma@gmail.com

    ABSTRACT
    Oral route of administration is most convenient route but often is disadvantageous for administering to geriatric and paediatric patients. Orally disintegrating film is found to be effective in delivering rapid drug action by dissolving the drug in buccal cavity. Since a decade oral thin films has got commercial importance in generic and non generic market projecting it as a multinational business asset. Current research in this field is found to be associated with industrialization and commercialization. Current article make an overview of not only technological changes in research and manufacturing but also gives an insight about growing market worldwide.

  • ADR MONITORING: AN ESSENTIAL NEED FOR BETTER HEALTH CARE AND SAFETY

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    ABOUT AUTHORS
    Annu*, Priyanka
    Department of Pharmaceutical Sciences,
    Maharshi Dayanand University, Rohtak, Haryana, India.
    *annu.gvm@gmail.com

    ABSTRACT
    Adverse drug reaction (ADR) is the noxious and unintended response that occurs at the dose of drug normally used for prophylaxis, diagnosis or therapy of disease. ADRs cause a huge burden on the modern society because of the increase incidence of the morbidity and mortality. ADRs can occur with any class of drugs and the availability of the more and more number of therapeutics increases the risk of ADRs consequently. It has been found that the maximum numbers of ADRs occur more among infants and children and also they are generally more severe as compared to adults. ADRs are of particular interest in today’s practice because clinical trials are done in the limited number of the subjects and therefore the drug which is found safer in the clinical trial may produces serious ADRs. The most common reason for this is that the clinical studies generally have limited sample size and have low statistical power. Therefore the ADRs monitoring is an essential need for the better health care and therefore the health care centre should promotes the spontaneous monitoring, reporting, documentation and prevention of ADRs.

  • A SHORT REVIEW ON ZIKA VIRUS PAST, PRESENT STRATAGIES AND FUTURE PROSPECTIVES

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    ABOUT AUTHORS
    M .Manasa Rekha1*, A. Bharath Kumar1, T.Mubeena1, C. Gopinath2
    1Department of Pharmacy Practice,

    Annamacharya college of Pharmacy, Rajampet, Andhra Pradesh, India.
    2Department of Phytopharmaceuticals and Pharmacognosy,
    Annamacharya college of Pharmacy, Rajampet, Andhra Pradesh, India.
    manasarekharoyal@gmail.com

    Zika virus(ZIKV) is a member of the virus family Flaviviridae and the genus Flavivirus and It is transmitted Aedes mosquitoes like A. aegypti and A. albopictus,which are active at day times[1,2].

  • REVIEW ON: INDIAN MEDICINAL PLANTS HAVING ANTICANCER PROPERTY

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    ABOUT AUTHORS
    Nandu Kayande*, Rakesh Patel
    Department of Pharmacy,
    OPJS University, Churu, Rajasthan, India
    * nandu_kayande@rediffmail.com

    ABSTRACT
    The traditional Indian medicine - Ayurveda, describes various herbs with anticancer as well as antioxidant properties. Various plant products have been used in treatment of cancer over the years. India is a peninsula of herbal hub, in which ayurvedics system of medicine has flourished as an enlightment in the field of Medicine. Currently medicinal plants have become the paramount source of drug discovery in research for treating diverse form of diseases including Cancer. In this review ayurvedas classical literature and evidence based research data were emphasized to explore the ayurvedic medicinal plants with potent anticancer activity.

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  • A REVIEW ON GASTRORETENTIVE DRUG DELIVERY SYSTEMS

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    ABOUT AUTHORS
    Hemendrasinh J. Rathod*, Dhruti P. Mehta, Jitendra singh Yadav
    Department of Pharmaceutics,
    Vidyabharti Trust College of Pharmacy,
    Umrakh, Gujarat, India.
    * hariomh.j.rathod@gmail.com

    ABSTRACT
    The purpose of writing the review on gastroretentive drug delivery systems (GRDDS) was to accumulate the current literature with a special emphasis on several gastroretentive approaches that have recently become important methodologies in the field of site-specific orally administered sustained/controlled release drug delivery. Technological efforts have been made in research and development of rate-controlled oral drug delivery systems to solve physiological difficulties, like short gastric residence times (GRT) and unpredictable gastric emptying times (GET). GRDDS are an approach to prolong the GRT, thereby targeting site-specific drug release in the upper gastrointestinal tract (GIT) for local or systemic effect. Conventional oral dosage forms pose low bioavailability problems because of their quick gastric transition from the stomach, particularly in case of drugs that are less soluble at an alkaline pH of the intestine. Also, drugs that produce their local action in the stomach get quickly emptied and don’t get sufficient residence time in the stomach. Several efforts have been made to extend the retention time of drug delivery system to reduce the frequency of dose administration. GRDFs not only prolong dosing intervals, but also increase patient compliance beyond the level of existing controlled release dosage forms. This article gives an overview on advantages, disadvantages and characterization of gastroretentive drug delivery systems. This review also includes commercially available gastroretentive products and patents.

  • CHROMATOGRAPHY BASED CHEMOMETRIC FINGERPRINTING, ISOLATION & QUALITY CONTROL OF PHYTOCHEMICALS

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    ABOUT AUTHOR
    Deepak chowrasia
    Institute of Pharmacy, CSJM University,
    Kanpur, Uttar Pradesh
    chowrasia.deepak@gmail.com

    ABSTRACT
    The present paper explores key consideration of different chromatographic procedures in phytochemical screening of natural products to investigate novel plant based therapeutically active compounds. Sophistication in instrumentation has sharpened the edges of chromatography making the technique an indispensable specialized laboratory as well as industrial tool for isolation, identification, and quality control of herbal products round the globe.

  • REGULATORY CANVAS OF INDIAN PHARMACEUTICAL INDUSTRY: CHALLENGES AND FUTURE

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    ABOUT AUTHORS
    Ayushi Srivastava*, Veena Gupta
    QC Department,
    Akums Drugs & Pharmaceuticals Ltd, Haridwar, India
    *ayushisr@gmail.com

    ABSTRACT
    This article undertakes a review and assessment of regulatory framework in the Indian pharmaceutical industry. Understanding the regulatory circumstances in this segment is extremely critical. The Pharmaceutical industry is one of the major industries in India and it contributes a large share in the overall macro level growth of the India. It is one of the most dynamic sectors in the country but its compliance structure is more complex. The pharmaceutical industry has always been a buoyant sector in the eyes of Investors. With increasing returns, lower risks and high growth, investors are more interested in this industry than ever before.

  • EXTRACTION AND PURIFICATION OF NUCLEIC ACID USING CBNP & PCIA TECHNIQUE

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    About Author
    Nirav Soni
    Department of Quality Assurance,
    A-One Pharmacy College,
    Anasan, Ahmedabad, Gujarat, India
    nirav_sonic@yahoo.com

    ABSTRACT
    Isolation of Nucleic acid easily by Solid Phase Extraction (SPE) and this approach, using commercially available Extraction of nucleic acid column-based kits, requires no toxic chemicals and is a rapid and consistent method for concomitant protein extraction. It is a modern technique useful for separation of Nucleic acid which is  most reliable, less time consuming and separation of  impurities and continuity of reactive products using listed techniques like column-based nucleic acid purification, Nucleic acid methods& ethanol precipitation, DNA separation by silica adsorption. Buffer choice is significant to completely solubilized all proteins in the sample. This technique provides a simple and effective way to analyze protein and nucleic acids simultaneously from the same sample not affecting yield and quality.

  • REVIEW: COMBINED CANDESARTAN CILEXETIL AND PIOGLITAZONE HYDROCHLORIDE THERAPY IN METABOLIC SYNDROME
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