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  • LYOPHILIZATION PROCESS - AN OVERVIEW

    ABOUT AUTHORS:
    *Naveen Kamboj1, Sadanand Maurya2, Sonia Kamboj3, Gaurav kumar Singh2
    1Chandigarh College of Pharmacy, Landran, Mohali, Panjab
    2Transalam Institute of Pharmaceutical Education and Reaserch, Meerut, Uttar Pradesh
    3ISF college of pharmacy moga, Punjab
    *kamboj.naveen21@gmail.com

    ABSTRACT
    The most important method for developing the very stable and suitable formulation for thermolabile as well as thermostable drug is lyophilization which works on the principle of sublimation of ice crystal from frozen material. Principle of the process through the basis of formulation, freezing, primary drying and secondary drying . In order to design optimum lyophilization process, process development scientific need to the critical properties of the formulation and how to apply to this information to process design. Lyophilized formulation not only has the advantage of better stability, but also provide easy handling i.e. shipping and storage. This article present an overview of lyophilization process, its advantage and pharmaceutical application.

  • DEVELOPMENT AND VALIDATION OF ANALYTICAL METHOD FOR METRONIDAZOLE AND NORFLOXACIN IN TABLETS DOSAGE FORM

    ABOUT AUTHORS:
    Yogesh Kumar Jain*, Dr. R.P.S. Rathore, Udaibhan Singh Rathore, Dharmendra Singh sisodiya,  Vijendra Singh Chauhan
    Bhupal Nobles’ College of Pharmacy,
    Udaipur – 313002, Rajasthan, India.
    *jain.yogesh1987@gmail.com

  • SUPERDISINTEGRANTS: A REVIEW

    About Authors:
    Hemant Rathod*, M.P.Khinchi, Dilip Agrawal, Natasha Sharma

    *Department of Pharmaceutics
    Kota College of Pharmacy,
    Kota, Rajasthan, India
    *hemant2787@gmail.com

    Abstract
    Fast dissolving, fast melting, chewable and orally dissolving or disintegrating tablets are solid dosage forms that disintegrate rapidly and dissolve in the mouth without water. These products have staying power in the marketplace because they appeal to consumers and support increased compliance among users as well as provide effective life-cycle management. The principle challenge with orally disintegrating tablets (ODTs) is to develop tablet formulations that deliver rapid disintegration, pleasant mouth feel and high breaking force for tablet robustness. Superdisintegrants affect a range of formulation parameters; including the rate of disintegration, tablet breaking force, and mouth feel i.e. Polyplasdone XL-10 superdisintegrant provides optimal performance in ODT formulations.

  • AN OVERVIEW: MELT-IN-MOUTH TABLETS

    About Authors:
    Hemant Rathod*, Shakti Shekhawat, Jimit Shah, Parth Gandhi
    Department of Pharmaceutics,
    Kota College of Pharmacy, Kota, Rajasthan.
    *hemant2787@gmail.com

  • NANOROBOTICS - AN EMERGING TREND FOR CANCER TREATMENT

    About Authors:
    Prabhakar Sharma*1, Prakash Pandey1, Ramchandra Gupta1, Ashish Garg2, Prateek Jain3
    1Department of Pharmacognosy
    2Department of Pharmaceutics
    3Department of Pharmacy
    Guru Ramdas Khalsa Institute of Science and Technology (Pharmacy) Jabalpur, M.P.
    *mr.pks19@gmail.com

    Abstract
    Size reduction is one of most fundamental unit operation which is of prime importance in pharmacy. It helps in improving stability and bioavailability, reducing toxicity, enhancing release and providing better formulation opportunities for drug. Nanotechnology involves the engineering of molecularly precise structures and,ultimately, molecular machines. This paper presents the study of nanorobotscontrol activation for stenosed coronary occlusion, with thepractical use of chemical and thermal gradients for biomedicalproblems. This review paper describes all the information about pharmaceutical nano-robots, their types, components mechanismetc.

  • NANOPARTICLE TECHNOLOGY IN DRUG DELIVERY SYSTEM

    ABOUT AUTHORS:
    Vishwa Deepak Kumar*, Abhishek Sharma, Rajneesh Mishra, Kanchan Sharma
    B.Pharmacy, 2nd year
    Department of Pharmacy, IEC group of institutions,
    Greater Noida (U.P) INDIA, Pin- 201301
    *vdkumar.iec@gmail.com

    ABSTRACT
    For the past few decades, there has been a considerable research interest in the area of drug delivery using particulate delivery systems as carriers for small and large molecules. Particulate systems like nanoparticles have been used as a physical approach to alter and improve the pharmacokinetic and pharmacodynamic properties of various types of drug molecules. They have been used in vivo to protect the drug entity in the systemic circulation; various polymers have been used in the formulation of nanoparticles for drug delivery research to increase therapeutic benefit, while minimizing side effects. Here, we review various aspects of nanoparticle formulation, characterization, effect of their characteristics and their applications in delivery of drug molecules and therapeutic genes. Nanoparticles are the preparations having size in nanometers.

  • FORMULATION AND CHARACTERIZATION OF MELOXICAM LOADED MICROEMULSION FOR THE TREATMENT OF RHEUMATOID ARTHRITIS

    ABOUT AUTHOR:
    Verma Siddharth
    Sri Ram Institute of Technology,
    ITI Jabalpur M.P. 482003
    luckyverma84@gmail.com

    ABSTRACT
    Rheumatoid arthritis (RA) is a chronic, systemic inflammatory disorder that may affect many tissues and organs, but principally attacks synovial joints. The process produces an inflammatory response of the synovium (synovitis) secondary to hyperplasia of synovial cells, excess synovial fluid and the development of pannus in the synovium. Various treatments are available. Non-pharmacological treatment includes physical therapy, orthoses, occupational therapy and nutritional therapy. Analgesia (painkillers) and anti-inflammatory drugs including steroids are used to suppress the symptoms, while disease-modifying antirheumatic drugs (DMARDs) are often required to inhibit or halt the underlying immune process and prevent long-term damage. In recent times, the newer group of biologics has increased treatment options.

  • OFFERING FLEXIBILITY OF EXPRESSION TO MEDICINE DESIGNERS

    About Authors:
    Madhulika Kabra1, Pramod Khatri2*, Neerja Gupta3
    1 Professor of Pediatrics,
    2,3 Department of Pediatrics,
    AIIMS Hospital, India
    *pramodsinghkhatri@gmail.com

  • PRESENT REVIEW- TRANSDERMAL DRUG DELIVERY SYSTEM

    About Author:
    Akshay Rajgaria

    Kanak Manjari Institute of Pharmaceutical Sciences
    akshaykrish2007@gmail.com

    ABSTRACT
    Transdermal drug delivery system (TDDS) provides a means to sustain drug release as well as reduce the intensity of action and thus reduce the side effects associated with its oral therapy. Transdermal drugs are self contained, discrete dosage form. Transdermal Drug Delivery System is the system in which the delivery of the active ingredients of the drug occurs by the means of skin. Skin is an effective medium from which absorption of the drug takes place and enters the circulatory system. Various types of transdermal patches are used to incorporate the active ingredients into the circulatory system via skin. The patches have been proved effective because of its large advantages over other controlled drug delivery systems.

  • STRUCTURE AND APPLICATION OF DENDRIMER IN NOVEL DRUG DELIVERY SYSTEM: A REVIEW ARTICLE

    About Authros:
    Khushbu Singh*1, Chandana Majee2
    1 M.Pharm ( department of pharmaceutics)
    2 Assistant Professor, department of pharmaceutical chemistry.
    Noida institute of engineering and technology, noida
    *khushbu1991singh@gmail.com

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