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  • ESTIMATION OF OXIDATIVE STRESS AND ANTIOXIDANT STATUS IN TYPE II DIABETIC PATIENTS

    About Authors:
    Samudrala Lahari

    St.Peters Institute Of Pharmaceutical Sciences,
    Kakatiya University
    plushylahari@gmail.com

    Abstract
    Background: Diabetes mellitus is a group of metabolic disorders characterized by hyperglycemia and abnormalities in carbohydrate, fat and protein metabolism. It results from defects in insulin secretion, insulin sensitivity or both. Oxidative stress may play an important role in the itiology of diabetes and Diabetic complications. So, during Diabetes hyperglycemia causes increased production of free radical especially reactive oxygen species(ROS) for all tissues from glucose auto-oxidation and protein glycosylation.

  • FIBRODYSPLASIA OSSIFICANS PROGRESSIVA

    ABOUT AUTHOR:
    Akshay Rajgaria
    Kanak Manjari Institute of Pharmaceutical Sciences
    Rourkela, Orissa
    akshaykrish2007@gmail.com

  • EVIDENCE-BASED MEDICINE TO PERSONALIZED MEDICINE – A PROSPECTIVE

    About Author:
    Pritish Dash
    Institute of Bioinformatics and Applied Biotechnology (IBAB)
    Bangalore, India
    pr4evr@gmail.com

    Abstract:
    Evidence-based medicine (EBM) is the process of systematically reviewing, appraising and using clinical research findings to aid the delivery of optimum clinical care to patients. It is a method of healthcare decision-making that intends to combine the most reliable scientific information with individual expertise and patient preferences in order to offer the optimal diagnostic and therapeutic option for the patient. On the other hand, pharmacogenomics is a whole genome application that examines the single gene interactions with drugs. In recent years, the term personalized medicine has been introduced to represent an approach considering differences among individual patients. In modern medicine, the most important sources of evidence are clinical trials using epidemiological methods, and molecular biological and genetic methods characterizing individual patients.
    This paper tries to review the rapid transformation of modern medicine from the ‘evidence-based medicine’ to ‘personalized and genomic medicine’.

  • 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.

  • HERBAL PLANTS A RELIABLE SOURCE FOR DRUG DISCOVERY AND DEVELOPMENT

    About Authors:
    Enegide Chinedu*, David Arome, Solomon F. Ameh
    Department of Science Laboratory Technology (Physiology & Pharmacology Technology),
    University of Jos, Jos Nigeria.
    *chinex.snow@gmail.com

    Abstract
    Though remarkable success have been achieved in the discovery and development of various drugs for the treatment and management of several ailments, there is still need for more discoveries. This is due to the reason that some of the drugs currently in use posseses one or more of the following drawbacks (i) high toxicity level (ii) increase lose of effectiveness or low efficacy (iii) costly or (iv) inaccessable. Herbs have now become the main stream for drug discovery and development. Conservative estimate have revealed that there are over 250,000 higher plant species, and only a minute proportion have been screened exhaustively for their possible therapeutic properties. Atleast, over 120 unique pharmacological substances derived from plants are currently being used as drugs in various countries in the world. Apart from the direct use of plant derivatives as therapeutic agents, they can also serve as models for the design, synthesis or semisynthesis of other therpeutic agents. In conclusion, herbs are a reliable source for more discovery and development of new drugs. The scientific community should therefore harness this resource by improving research on it.

  • A REVIEW ARTICLE ON TRANSDERMAL DRUG DELIVERY SYSTEM

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

  • FORMULATION AND CHARACTERIZATION OF RALOXIFENE BETA-CYCLODEXTRINE INCLUSION COMPLEX FOR SOLUBILITY ENHANCEMENT

    ABOUT AUTHORS:
    Gazi Juned M.*1, Javia A.R1, Sheth A.K1, Sachinkumar P. Chauhan, Nirmal Shah
    1Department of Pharmacy, Sumandeep Vidyapeeth University,
    At & Po Pipariya, Ta.- Waghodia, Dist. Vadodara-391760.
    (Gujarat) India
    gaziriju89@gmail.com

  • DEVELOPMENT AND VALIDATION OF IR SPECTROPHOTOMETRIC METHOD FOR ESTIMATION OF AZELASTINE HYDROCHLORIDE IN NASAL SPRAY PREPARATIONS

    ABOUT AUTHORS:
    *1Patel Rina B., 2Patel Nilam K.
    1M.pharm(Q.A), Department of Pharmaceutical Sciences
    Hemchandracharya North Gujarat University,
    2Asst. Professor, Dept. of Pharmaceutical Sciences
    Department of Pharmaceutical Sciences, Hemchandracharya North Gujarat University, Patan. Gujarat-384265
    *rina_patel2003@yahoo.com

    ABSTRACT
    A simple, sensitive, rapid, accurate, precise and economical Fourier transform infrared (FTIR) spectrophotometric method has been developed for the determination of Azelastine Hydrochloride (AZH)   in nasal spray preparations. The IR spectrophotometric method was based on the determination of AZH by the measurement of the area of the infrared band corresponding to the carbonyl group centred at the band1636 cm-1. It was present in the AZH but not in Acetonitrile used as solvent and highest intensity was at the area 1701.08-1584.21 cm-1. The linearity of AZH was obtained in the concentration range of 5-100 μg/ml. The mean % recovery was 99.67 ± 0.57 %. The recovery studies confirmed accuracy of proposed method and low values of standard deviation confirmed precision of method.

  • A VISIT ON PHARMACEUTICAL INDUSTRIAL ORIENTATION

    About Authors:
    Dr. D.k. Sanghi, Rakesh Tiwle*, Puja Karanjekar, Priyanka Hemne, Dileshwari Madavi, Padma Tembhre
    Shri Laxmanrao Mankar Institute of Pharmacy,
    Amgoan, Gondia, Maharashtra, India- 441902.
    rakesh_tiwle@rediffmail.com

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