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Andhra Pradesh

 

Clinical courses

  • A REVIEW ON ANALYTICAL METHOD DEVELOPMENT AND VALIDATION OF PHARMACEUTICAL TECHNOLOGY

    ABOUT AUTHORS:
    Rajani Pathuri*, M.Muthukumaran, B.Krishnamoorthy, Amreen Nishat
    Montessori Siva Sivani Institute of Science & Technology-College of pharmacy
    Mylavaram, Vijayawada, Andhrapradesh-521230
    *rajani.prakash4@gmail.com

    ABSTRACT
    Analytical methods development and validation play important roles in the discovery, development and Manufacture of pharmaceuticals. Method development is the process of proving that an analytical method is acceptable for use to measure the concentration of an API in a specific compounded dosage form which allow simplified procedures to be employed to verify that an analysis procedure, accurately and consistently will deliver a reliable measurement of an active ingredient in a compounded preparation. The analytical method validation is essential for analytical method development and tested extensively for specificity, linearity, accuracy, precision, range, detection limit, quantization limit, and robustness. In summary, analytical method development and validation allows to confirm that an accurate and reliable potency measurement of a pharmaceutical preparation can be performed. 

  • THE ROLE OF NEW GENERATION PHYTO HORMONES: AN OVERVIEW

    ABOUT AUTHORS:
    Lohithasu Duppala*, Santhosh naidu Matsa, Manikumar Kothakota,

    GITAM Institute of Pharmacy, GITAM University, visakhapatnam, Andhra Pradesh, India-530045.

    lohithasu@gmail.com, +91-9491894432

    ABSTRACT:
    Generally, almost all communication in higher plants was thought to be mediated by the five classes of classical plant hormones  i.e. auxins, cytokinins,  gibberellins, abscisic acid and ethylene. The plant hormone action thus appeared to be basically different from that in animals. This article discusses the general role for new generation of plant hormones includes Brassinosteriods, Salicylic acid. Peptides,Polyaminesand Jasmonates.

  • A CRITICAL REVIEW ON CALIBRATION OF ANALYTICAL INSTRUMENTS

    About Authors:
    Manoranjan Thunuguntla*, B.Krishnamoorthy, M.Muthukumaran, Amreen Nishat, Vasu Naik
    Montessori Siva Sivani Institute Of Science & Technology College Of Pharmacy,
    Mylavaram, Krishna District,
    Andhra Pradesh

    * manozph@gmail.com

    Abstract1:
    Analytical instruments are used for specific analysis of drugs and pharmaceuticals. So, regular performance verification is made to ensure that instrument used in the analytical purpose should be properly calibrated and validated “to demonstrate that it is suitable for its intended purpose”. This article is prepared in the sense to get all the information on calibration of basic analytical instruments in laboratory and industrial scale of scientific institutions. The scope of this article is to get the procedures of calibration of analytical instruments at here. Calibration of instruments with their procedure and precautions of Thermometer, Ph Meter, Karl Fisher, Polarimeter, Conductivity Meter, Tablet Fraibilator, Hardness Tester, Disintegration Test Apparatus, Dissolution Test Apparatus, Potentiometer and U. V. Spectrophotometer are mentioned below.

  • DISCUSSION ON THE ROLE OF Rb PROTEIN AND P53 IN CELL CYCLE REGULATION

    About Authors:
    Lohithasu Duppala* , Manikumar Kothakota
    GITAM Institute of Pharmacy,
    GITAM University, visakhapatnam, Andhra Pradesh, India-530045.

    * lohithasu@gmail.com, +919491894432

    INTRODUCTION:
    Cell Theory:

    · All organisms consist of one  or more cells.
    · Cell is the smallest unit of life.
    · All cells come from pre-existing cells.

    Cell cycle:
    The dividing and non –dividing stages in the life of a cell are described by a series of events called the cell-cycle. The cell cycle  is the sequence of events by which a cell duplicates its genome and divides into daughter cells.Some cells, like skin cells ,divide continuously throught the life of the organism.Cardiac muscle cells are arrested in G2 phase.

  • Opening Sales Manager in Reputed Hyderabad based MNC

    26 years of successful presence in the pharmaceutical industry; Focused on manufacture of APIs, contract research and contract manufacturing
    2 US FDA inspected manufacturing facilities
    Over 400 DMFs worldwide; with a presence in over 85 countries
    40,000 sq. ft. state-of-the-art R&D facility at Hyderabad
    Over 1000 employees

    Post: Sales Manager

  • ETHYL CELLULOSE BASED GLIBEMCLAMIDE CONTROLLED RELEASE MATRIX TABLETS

    ABOUT AUTHORS:
    P.PRATHYUSHA*
    Department of Pharmaceutics,
    Raghavendra Institute of Pharmaceutical and Educational Research,
    Anantapur, A.P, India.
    * prathyusha2012@gmail.com

    ABSTRACT
    In the present investigation, an attempt was made to formulate the Oral Controlled Release Matrix Tablets of Glibenclamide in order to improve efficacy, reduce the frequency of administration, reduce dose related side effects and better patient compliance. Four formulations were prepared by wet granulation method using Ethyl cellulose and as a polymer in the ratio of 1:1, 1:2 and 1:4 and Conventional Tablets by using  Starch mucilage as a granulating agent. The formulated granules showed satisfactory flow properties. All the tablets formulation showed acceptable pharmaco technical properties and complied with pharmacopoeial standards. The tablets were evaluated for weight variation, hardness, friability, drug content and invitro dissolution studies. In- vitro release studies were carried out at pH1.2 for first 2 hrs followed by phosphate buffer at pH7.4 over a period of 12hrs using USP dissolution apparatus. F3 shows good initial release of 25.2% in 1 hr and may extend release of 96.8% in 12 hrs. Different release models like zero order, first order, higuchi, Hixson-Crowell and krosmeyer-peppas were applied to invitro drug release data in order to evaluate the drug release mechanisms and kinetics. Formulated matrix tablets were compared with conventional and marketed (diaonil 5mg) formulations. Matrix tablets with optimum concentration of Ethyl cellulose were successfully developed and evaluated.

  • Vacancy for Director - Cell Biology in United States Pharmacopeia

    The United States Pharmacopeia (USP) is a non–governmental, official public standards–setting authority for prescription and over–the–counter medicines and other healthcare products manufactured or sold in the United States. USP also sets widely recognized standards for food ingredients and dietary supplements.

  • Job as Assistant Manager- DQA in Mylan

    Mylan is one of the world’s leading generics and specialty pharmaceutical companies, providing products to customers in more than 150 countries and territories. The company maintains one of the industry’s broadest and highest quality product portfolios, which is regularly bolstered by an innovative and robust product pipeline.

  • Job as LAB HELPER / ATTENDANT in Centre for DNA Fingerprinting and Diagnostics

    The Centre for DNA Fingerprinting and Diagnostics (CDFD), Hyderabad is a premier autonomous R & D Institute under the Societies Act funded by the Department of Biotechnology, Ministry of Science and Technology, Government of India, that has been established to provide services and to undertake R & D in DNA Fingerprinting, DNA Diagnostics and other areas of modern biology.

  • Mylan invites M.Pharm, M.Sc as Officer / Executive - Pharmacovigilance

    Mylan is one of the world’s leading generics and specialty pharmaceutical companies, providing products to customers in more than 150 countries and territories. The company maintains one of the industry’s broadest and highest quality product portfolios, which is regularly bolstered by an innovative and robust product pipeline.

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