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Pharma Courses
  • INTRODUCTION TO STEM CELL CRYOPRESERVATION – A NEWER PHENOMENON OF ENSURING THE LONGEVITY OF CHILD HEALTH: A CLINICAL REVIEW

    About Authors:
    Mr. Satyanand Tyagi*, Raghvendra1, Amlan Mishra2, Patel Chirag J3, Asheesh Singh4
    *President, Tyagi Pharmacy Association & Scientific Writer (pharmacy), Chattarpur, New Delhi, India-110074.
    Prof. Satyanand Tyagi is a life time member of various pharmacy professional bodies like IPA, APTI and IPGA. He has published various research papers and review articles. His academic works include 51 Publications (43 Review Articles and 08 Research Articles of Pharmaceutical, Medicinal and Clinical Importance, published in standard and reputed National and International Pharmacy journals; Out of 51 publications, 11 are International Publications).
    He has published his papers almost in different specialization of Pharmacy field...His research topics of interest are neurodegenerative disorders, diabetes mellitus, cancer, rare genetic disorders as well as epilepsy.
    1
    Department of Pharmaceutics, Aligarh College of Pharmacy, Aligarh, U.P, India-202001.
    2Department of Pharmacology, Smt. Vidyawati College of Pharmacy, Jhansi, U.P, India-284128.
    3Department of Pharmaceutics, Maharishi Arvind Institute of Pharmacy, Mansarovar, Jaipur, Rajasthan, India-302020.
    4Research Associate, Center for Research and Development, Ipca Laboratories Ltd Ratlam, Madhya Pradesh, India-457114.

    *sntyagi9@yahoo.com,
    +91-9871111375 / 9582025220

    ABSTRACT:
    The umbilical blood cord being rich in stem cells needs to be preserved by means of a new technique called cryopreservation. The Process whereby whole tissues or cells are preserved by cooling at very low temperatures is known as Cryopreservation. Stem cell cryopreservation is a relatively new phenomenon; it is one way of ensuring the longevity of child’s health. This is done by banking the baby’s umbilical cord blood affluent with stem cells. Stem cells are important as they can grow into tissues, even organs like the heart or liver. What is more, they have the awesome potential to revamp damaged tissues.

    Till date, over seventy diseases have been successfully treated with the help of stem cell stored in the cord blood. Research on stem cells has, by no means, abated. Scientists realizing their potential and worth are carrying out intensive research on their uses as well as ways preservation. Before preserving stem cells, a biological test is carried out to eschew the possibility of deadly diseases like various types of Hepatitis or HIV. That done, the cord blood cells are now stored by means of the technique under discussion- Cryopreservation. This technique involves adding a cryopreservant that lets the blood freeze gradually. The blood is frozen to sub-zero degree temperatures so that biochemical reactions or any other dangerous biological that could cause cell death may be arrested. Typically, the cells are stored at temperatures as low as -196, – 156, or – 120 degrees centigrade. Freezing stem cells through cryopreservation at such low temperatures is supposed to ensure their longevity. Let it be known, however, that scientists are still divided over the optimum temperatures as well as the efficacy of the cryopreservation technique itself. The aim of present article is to provide in depth knowledge about this technique of preserving stem cells of child i.e. the technique so called “Cryopreservation”. An attempt is also made to focus how this technique ensures the longevity of child’s health.

  • NANOTECHNOLOGY: NANOCRYSTALS

    About Authors:
    Patel Chirag J*, Asija Rajesh, Asija Sangeeta
    Maharishi Arvind Institute of Pharmacy, Department of Pharmaceutics, Jaipur.
    *chirag.bangalore@gmail.com

    ABSTRACT
    Oral delivery of drugs with poor aqueous solubility and poor enzymatic and/or metabolic stability is very challenging. However, the advent of nanotechnology has revolutionized the field of oral drug delivery. Development of poorly soluble and/or permeable drug molecules using nanocrystal formulations has proven to be highly successful due to the greater surface/volume ratio, resulting in improvements in dissolution and bioavailability as well as enhanced permeability.The industrially relevant bottom up (precipitation) and top down production technologies (pearl milling, high pressure homogenization, and combination technologies) are presented. This review discusses drug loading among various nanoparticles, method of preparation, evaluation and success of nanocrystals compared to other nanotechnologies.

  • GATE PY – 1993 Question Paper

    PART – A

    SECTION – I

  • GATE PY – 1992 Question Paper

    PART-A

    SECTION – I

  • ANALYSIS BY INSTRUMENTAL ANALYTICAL METHODS

    About Authors:
    Kapil Sharma*1, Subhash Gupta2
    1Yaresun Pharmaceutical Pvt. Ltd.,India.
    2Oasis test house ltd.jaipur-302006,rajasthan,india.
    *pharma_kapil@rediffmail.com

    INTRODUCTION
    Most of the manufacturing industries rely upon both qualitative and quantitative chemical analysis to ensure that the raw material used meet certain specification, and also to check quality of the final product. The unwanted compound may be harmful to manufacturing process or may appear as a harmful impurity in the final product.1

    A quantitative analysis is performed to establish the proportion of the essential component in the raw material. The final manufactured product is analyzed to ensure that its essential component is present within a predetermined range of composition and impurities do not exceed certain specified limit.

  • DIFFERENT METHODS OF ENHANCEMENT OF SOLUBILIZATION AND BIOAVAILABILITY OF POORLY SOLUBLE DRUGS: A RECENT REVIEW

    About Authors:
    Patel Chirag J*, Asija Rajesh, Asija Sangeeta
    Maharishi Arvind Institute of Pharmacy, Department of Pharmaceutics,
    Jaipur, Rajasthan.
    *chirag.bangalore@gmail.com

    ABSTRACT
    Solubility, the phenomenon of dissolution of solute in solvent to give a homogenous system, is one of the important parameters to achieve desired concentration of drug in systemic circulation for desired pharmacological response. Low aqueous solubility is the major problem encountered with formulation development of new chemical entities as well as for the generic development. The insufficient dissolution rate of the drug is the limiting factor in the oral bioavailability of poorly water soluble compounds. This review discusses BCS classification, carriers for solubility enhancement and different techniques for solubility enhancement.Various techniques are used for the enhancement of the solubility of poorly soluble drugs which include micronization, nanonization, sonocrystallization, supercritical fluid method, spray freezing into liquid and lyophilization, evaporative precipitation into aqueous solution, use of surfactant, use of co-solvent, hydrotropy method, use of salt forms, solvent deposition, solubilizing agents, modification of the crystal habit, co-crystallisation, complexation and drug dispersion in carriers.Selection of solubility improving method depends on drug property, site of absorption, and required dosage form characteristics.With the advent of combinatorial chemistry and a high throughput screening, the number of poorly water soluble compounds has increased solubility. A success of formulation depends on how efficiently it makes the drug available at the site of action.The purpose of this review article is to describe the techniques of solubilization for the attainment of effective absorption with improved bioavailability.

  • 3 Day National Level Workshop On Computer Aided Drug Designing & Chemoinformatics, 28-30th Sept 2012

    RASA Life Science Informatics

    Invites you to 3 Day Workshop in In-Silico Drug Discovery and Advance Chemoinformatics (28th-30th Sept. 2012).
    Space is limited, so be sure to enroll now!

    [adsense:336x280:8701650588]

    Salient Features of the Workshop
    Workshop groups will study problems with hands-on examples using computational chemistry methods and discuss issues highlighted by examples and Case Studies in drug discovery presented by instructors. A Case Study set with a focus on chemical database creation and filtering drug like compounds will be used to link all workshop activities throughout the workshop.

    On completion of this workshop you will be expertise in :
    * Hands on training on commercial softwares of Drug discovery
    * Application  of Chemoinformatics in drug discovery
    * Interaction and guidance from eminent scientist & professionals  from industry & research labs
    * Training from industry expertsfrom Chemoinformatics & drug discovery  informatics domain.
    * Analyzing chemical fingerprint
    * Pharmacophore based Virtual Screening of compounds
    * Screening of library compound against selected target
    * Analyzing Docking Results
    * Molecular Modeling &Dynamics
    * Steps involved from Lead Optimization to Final Candidate Drug.
    * Generating Knowledge from structure and different chemical databases
    * Using various chemical structure drawing and visualization tools
    * Digitizing your chemical Data.
    * Storing molecules in wide array of format
    * Awards for top 2 groups

    Speakers:

    Mr.Sameer Chaudhary, MD, RASA Life Science Informatics

    Mr. Rajeev Gangal, Associate Director, Medical Chemistry, Sai Advantium Pharma Ltd

    Mr. Jakir Pinari, Associate Director –DMPK, Sai Advantium Pharma Ltd

    Mr. Priyadarshini Waman Gadade, Sai Advantium Pharma Ltd

    Dr. K.V. Swamy, HOD, Dr.D.Y. Patil Biotech and Bioinformatics

    Audience
    Graduate/ post-graduate students, professionals, faculties from Organic chemistry, Pharmacy, Bioinformatics, Biotechnology, Agrochemical, Microbiology, Chemical ,life sciences etc from  Industries and institutions will benefit the most from getting hands-on experience

    Venue:
    Alard Charitable Trust
    Alard school of Pharmacy, Survey No. 50, Marunje,
    Near Rajiv Gandhi IT Park, Hinjewadi, Pune - 411 057,
    Maharashtra, India
    Tel:  02065600408, 07875692349/7875793891

    For any queries contact us at
    RASA Life Science Informatics

    301, 3rd Floor, Dhanashree Apartment,
    Opposite Chittaranjan Vatika, Model Colony,
    Shivaji Nagar, Pune - 411016.
    Tel:  02065600408, 07875692349/7875793891/8411927535
    or email us at workshop@rasalsi.com

  • METHOD DEVELOPMENT AND ITS VALIDATION FOR ESTIMATION OF DEFLAZACORT IN TABLET DOSAGE FORM BY UV SPECTROPHOTOMETRY

    About Authors:
    Kapil Sharma*1, Subhash Gupta2, Priyanka Sharma1
    1Yaresun Pharmaceutical Pvt. Ltd.,India.
    2Oasis test house ltd.
    jaipur-302006,rajasthan,india.
    *pharma_kapil@rediffmail.com

    ABSTRACT
    This paper describe a simple, precise and economical spectrophotometric method for the quantitative determination of Deflazacort(DFCT) in tablet dosage form. Method is based on the estimation of DFCT in aqueous acetonitrileat 246 nm. Beer’s law was obeyed in the concentration range of 4-14 µg/ml. The accuracy of the method was assessed by recovery studies and was found to be 99.38±0.15 for DFCT. Results of the analysis were validated statistically so that it can be used for routine analysis of DFCT in tablet dosage form.

  • Vertigo Management – Mapping prevalence and treatment. Understanding once a day preparation usage and place in therapy.

    About Authors:
    Indraneel sinha*, Mr. Sanjay sahai, Mr. Sunil jajoo, Mr. Abhijeet bhatkar
    Post graduate diploma in pharmaceutical management,
    Indian institute of health management research,
    jaipur
    *indraneel.sinha.999@gmail.com

    COMPANY PROFILE
    Sun Pharmaceuticals was set up in 1983 and the company started off with only 5 products to cure psychiatric illness.  Sun Pharma is best known worldwide as the manufacture of specialty Active Pharmaceuticals Ingredients (API) and formulations.

    However, the company is also concerned with chronic treatments such as cardiology, psychiatry, neurology, gastroenterology, diabetology and   respiratory ailments. Active Pharmaceuticals Ingredients (API) includes peptides, steroids, hormones, and anti?cancer drugs and their quality is internationally approved. Mr. Dilip S. Shanghvi is the Executive Chairman and Managing Director of Sun Pharma and Mr. Kamalesh H. Shah is the secretary.

  • SIMULTANEOUS ESTIMATION OF ATORVASTATIN AND AMLODIPINE IN RAW MATERIAL AND IN COMBINED TABLET DOSAGE FORM BY RP-HPLC

    About Authors:
    Kapil Sharma*1, Subhash Gupta 2
    1 Yaresun Pharmaceutical Pvt. Ltd.,India.
    2 Oasis test house ltd. Jaipur-302006, Rajasthan, India.

    *pharma_kapil@rediffmail.com

    ABSTRACT
    A method for simultaneous estimation of Atorvastatin (ATVS) and Amlodipine (AMLD) in raw material and in combined tablet dosage form has been developed. The method employs the application of RP-HPLC. Chromatgraphy was carried out on a nucleosil C-18,250 x 4.6 mm column using a mixture of phosphate buffer and methanol  (50:50 v/v)  as the mobile phase at a flow rate of 1.3 ml/min.  Run time was 15 min.  Detection was done at 245 nm and retention time of ATVS was 6.97 min and 3.96 min of AMLD.3  This method produced linear responses in the concentration range 20-140 µg/ml and 10-70 µg/ml for ATVS and AMLD respectively. The accuracy of the method was assessed by recovery studies and was found to be 100.54± 0.19 and 100.08±0.80 for ATVS and AMLD respectively.The procedure was successfully applied for the simultaneous determination of both drugs in laboratory prepared mixture of raw material and in market available tablet dosage form. Results of the analysis were validated statistically so that it can be used for routine analysis of ATVS and AMLD in combined tablet dosage form.4-6

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