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  • CLEANING VALIDATION IN PHARMACEUTICAL INDUSTRY: A COMPREHENSIVE APPROACH

    ABOUT AUTHORS:
    Sharma A*, Vaghela J.S, Sharma P, Sharma B, Agrawal M, Jagiwala S
    Department of Quality Assurance, Bhupal Nobles’ College of Pharmacy,
    Udaipur- 313002, Rajasthan, India
    *life4abhishek@gmail.com

  • BUTEA MONOSPERMA A TRADITIONAL MEDICINAL PLANT: - AN OVERVIEW

    About Authors:
    Sunil Roshan1, Prabhakar Sharma*1, Ramchandra Gupta1, Sudhakar Sharma2
    1Department of Pharmacognosy, GRKIST (Pharmacy)
    2Takshashila Institute Of Science And Technology
    Jabalpur, M.P.
    *prabhakar.sharma071026@gmail.com

    Abstract
    The traditional systems of medicine together with homoeopathy and folklore medicine continue to play a significant role largely in the health care system of the population. Butea monosperma(palas) belonging to the family leguminosae grown wildly in many parts of India. The plant is highly uses by the rural and tribal people in curing various disorders. Flowers are used as drug in many ailments like eye disease, chronic fever, enlargement of spleen, leucorrhoea, epilepsy, leprosy, antifungal activity, anti-inflammatory activity, liver disorders antifertility activity and gout etc. The plant parts are used in the form of extract, juice, infusion, powder and gum. The present paper enumerates various pharmacognostic and pharmacological aspects of the plant. This review also summaries the therapeutic potential of this plant.This is a moderate sized deciduous tree which is widely distributed throughout India, Burma and Ceylon, popularly known as 'dhak' or 'palas', commonly known as ‘flame of forest’. In this review an attempt has been done to highlight the work on Butea monosperma having pharmacological potential.

  • A REVIEW ON RECENT TRENDS IN ORAL DRUG DELIVERY- MOUTH DISSOLVING FORMULATION

    ABOUT AUTHORS:
    Manish Goswami, U.K.Singh, Rajat Kumar
    Kharvel subharti college of pharmacy (swami Vivekanandsubharti University) Subhartipuram,
    N.H-58, Meerut By Pass Road,
    Meerut, uttarpradesh- 250001, India.
    *manish.revosys88@gmail.com

    ABSTRACT:
    The desire of improved palatability in orally administered products has prompted thedevelopment of numerous formulations with improved performance and acceptability. Mouth dissolving tablets (MDTs) have received ever-increasing demand during the last fewdecades, and the field has become a rapidly growing area in the pharmaceutical industry. Theunique property of mouth dissolving tablet is that they are rapidly disintegrating and/ordissolving and release the drug as soon as they come in contact with saliva, thus obviate therequirement of water during administration. this review also provides the detailed concept of some unique patents; technologiesdeveloped and marketed formulations of Mouth Dissolving Tablets(MDTs).The present investigation was undertaken with a view to develop mouth-dissolving tablets which offer a new range of product having desired characteristics and intended benefits. Mouth dissolving tablets are advantageous particularly for pediatric, geriatric and mentally ill patients who have difficulty in swallowing conventional tablets and capsules. The basic approach used in development of MDT is the use of super disintegrants like Crosslinked carboxymethyl cellulose (Croscarmellose), Sodium starch glycolate (Primogel, Explotab). Polyvinylpyrrolidone (Polyplasdone) etc. whichprovide instantaneous disintegration of tablet after putting on tongue, thereby releasing the drug in saliva.

  • AN OVERVIEW: ON SUPERDISINTEGRANTS

    ABOUT AUTHORS:
    Rahul Tiwari*1, R.C. Jat1, Narendra Sharma1, Arvind Singh Rathore1
    1Shri Ram College Of Pharmacy,
    1Banmore, Morena, India -476444
    *rt30022@gmail.com, arvindsingh.rathore21@gmail.com

    ABSTRACT
    Disintegrants are substances or mixture of substances added to the drug formulation that facilitates the breakup or disintegration of tablet or capsule content into smaller particles that dissolve more rapidly than in the absence of disintegrants. In dosage forms, solid orals gain maximum popularities, about 85%, because of many advantages over others. The therapeutic activity of these formulations is obtained through a typical manner like disintegration followed by dissolution. Hence disintegration has major role for facilitating drug activity and thus gain popularity among other dosage forms. Superdisintegrants are generally used at a low level in the solid dosage form, typically 1-  10 % by weight relative to the total weight of the dosage unit. The present study comprises the various kinds of superdisintegrants which are being used in the formulation to provide the safer, effective drug delivery with patient's compliance. In this review article, more emphasis is given on application and usage of various superdisintegrants comparing with other disintegrants in reference to available scientific studies. The various sources of superdisintegrants and their modification to improve disintegration property are also high-lighted.

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  • miRNAs A NOVEL TARGET FOR ANTICANCER THERAPY

    ABOUT AUTHORS:
    Ketan M. Parmar*, Ritesh N. Sharma
    S.K.Patel College of Pharmaceutical Education & research,
    Department of Pharmaceutical chemistry, GANPAT UNIVERSITY.
    *brave_student_90@yahoo.com

    ABSTRACT
    With the development of technologies to look at the expression levels of hundreds of miRNAs at a time and the clear role of miRNAs in cancers, groups began looking at miRNAs profiles of different cancers,especially the circulating miRNAs. We intended to make sure whether circulating miRNAs could be a promising biomarker of human cancers. Method: We comprehensively searched the Cochrane Library, Medline and EMbase from 1966 to Nov 2009 for the following terms: (“miRNA” or “microRNA”) and (“tumor” or “carcinoma”) and (“plasma” or “serum” or “circulating”). Detailed information was extracted from studies that met the inclusion criteria: blood-based miRNAs in human cancers and studies published in the English literature. Results: The current review show that different researches use different measurement methods which might impact the results;Cancers treatment might have an effect on circulating miRNAs; some miRNAs are multi-faceted RNA; small sample size might produce selection bias. Furthermore, because of the lack of randomized controlled trials and the heterogeneous nature of the available data, no attempt was made to perform quantitativemeta-analyses.
    In this review, based on those researches, circulating miRNAs are promising and difficulties for their future application for diagnosing human cancers.

  • REVIEW: SUSTAINED RELEASE DOSAGE FORMS

    ABOUT AUTHOR:
    Abhijeet Welankiwar.
    Govt. College of pharmacy
    kathora naka Amravati (Maharashtra) 444604.
    abhi123welankiwar@gmail.com

    ABSTRACT:
    The oral route of drug delivery is typically considered the preferred and most patient-convenient means of drug administration. With many drugs the basic Goal of therapy is to achieve a steady-state blood or tissue level that is therapeutically effective and nontoxic for an extended period of time. Sustain release system are considered a wiser approach for the drugs with short half-lives and which require repeated dosing, they are easy to formulate and are irrespective of absorption process from gastrointestinal tract after oral administration. The basic objective of these dosage forms is to optimize the delivery of medications so as to achieve a measure of control on therapeutic effect in the face of uncertain fluctuations in the in vivo environment in which drug release takes place. The advances in the formulation technology of modified release dosage form with sustained release oral dosage form has been widely accepted approach as compared to conventional immediate release formulations of the same drug, over which it provides a prolong release of the drug over extended period of time there by giving the better patient compliance and enhanced bioavailability and resulting blood concentration-time profiles of drugs that otherwise suffer from few limitations.

  • Antimicrobial activity of Cymbopogon Species against Human Pathogens

    ABOUT AUTHOR
    Rudra Sharan Dwivedi *
    Bhopal University,
    Working in RMS Regrow, Pune
    * rudsd1987@gmail.com

  • REVIEW ON ONCOLYTIC VIRUS

    ABOUT AUTHORS
    Ashwini Dhusiya, Ritu Mahajan,
    Mahakal Inatitute of Pharmaceutical Studies, ujjain
    Madhya Pradesh
    .
    *ashwinidhusiya@gmail.com

    ABSTRACT
    Oncolytic virus is a wonderful discovery of 21st century. The basic concept of Oncolytic virus was developed since 1946 but it was not produce its effect properly. Now latest technology and modern biotechnology introduce a very efficient Oncolytic virus. This is a genetically modified virus that can treat various type of cancer with fewer side effects than other treatment of cancer. It follows different mechanism of killing tumor by specifically replication; induction of tissue necrosis factor; activation of immunity and treat incurable cancer even in metastatic stage of cancer so it is also effective in leukemia. Oncolytic virus therapy is undergoing in clinical trial and shows better results.
    This article covers brief knowledge of cancer, Virus and Oncolytic virus. It is helpful to understand history, mechanism, benefits and clinical data of Oncolytic virus. And a summary of marketed product ready to launch in near future.

  • A REVIEW ON MÖSSBAUER SPECTROSCOPY

    About Authors
    Deepak Kumar Shukla*, Nazia Shahid, Vikas Kumar Alaria
    Rajasthan Pharmacy College, Bhankrota, Jaipur (Raj.)
    *deepakshukla.pharma@gmail.com

    Abstract
    Over the past several years spectroscopy has become the preeminent technique for determining the structure of organic compounds. The study of recoilless nuclear resonant absorption or fluorescence is more commonly known as Mossbauer spectroscopy. From its first origins in 1957, it has grown rapidly to become one of the most important research methods in solid-state physics and chemistry. Mossbauer spectroscopy uses the nuclear properties to get information regarding the environment surrounding the nucleus. This technique is now valid application in diverse fields, such as solid state physics, metallurgy, chemistry and biochemistry. For example, it is possible to use this method for estimating the iron or tin content in ores, alloys and wasters in a non-destructive manner to concentration down to 0.03 percent in a short time of  the order of 10 minutes. The technique can also detect the relative percentage of  different charged states of the same atom, for example fe2+ and Fe3+ present in the material. This is somewhat difficult to get from any other technique.

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  • SURFACTANTS AND ITS APPLICATION IN PHARMACEUTICALS: AN OVERVIEW

    About Author:
    Dhananjay S Jadhav*
    M.Tech (Pharmaceutical Technology), Division of Pharmaceutical Technology,
    Institute of Chemical Technology, North Maharashtra University, Jalgaon -425001.
    Maharashtra, India
    * dhananjaysjadhav@hotmail.com

    Abstract
    Recently, surfactants have become one of the most important chemical products. They have become a subject of research, and their production and their use are on the increase. This wide range of properties, uses for surfactants in pharmaceutical products and systems is to try and introduce and explain in the subject of this article. Wetting of Solids, Solubilization, Emulsification, Dispersion of solid in solution, Micellization & Detergency all these are properties of surfactant. Surfactants are classified according to their polar head group, the charged head referred as Ionic surfactants and uncharged surfactants are generally referred to as nonionic surfactant. Because of their unique functional properties, surfactants find a wide range of uses in pharmaceutical preparations. These include, depending on the type of product, improving the solubility or stability of a drug in a liquid preparation, stabilizing and modifying the texture of a semisolid preparation, or altering the flow properties of a granulate, thus aiding in the processing of the final tablet dosage form. In addition to their use as excipients to improve the physical and chemical characteristics of the formulation, surfactants may be included to improve the efficacy or bioperformance of the product. The properties of surfactants are such that they can alter the thermodynamic activity, solubility, diffusion, disintegration, and dissolution rate of a drug. Each of these parameters influences the rate and extent of drug absorption. Furthermore, surfactants can exert direct effects on biological membranes thus altering drug transport across the membrane. The overall effect of inclusion of a surfactant in a pharmaceutical formulation is complex and may be beyond those initially intended. Surfactants may reduce the effectiveness of antimicrobials or preservatives included in a formulation.

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