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  • FORMULATION AND EVALUATION OF SUSTAINED RELEASE TABLETS FROM SOLID DISPERSIONS OF LOVASTATIN

    About Authors:
    Khayyam Shaikh*, Patwekar Shailesh, Santosh Payghan, John Disouza
    Department of Pharmaceutics,
    Tatyasaheb Kore College of Pharmacy,
    Warananagar, Kolhapur, Maharashtra, India 416113.
    *ramzanshek0587@gmail.com

    ABSTRACT
    During the last two decades there has been a remarkable increase in interest in sustained release drug delivery system. This has been due to various factors viz. the extensive cost of developing new drug entities, expiration of existing international patents, discovery of new polymeric materials suitable for prolonging the drug release, and improvement in therapeutic efficacy and safety achieved by this delivery system. A number of design options are available for the preparation of controlled release formulations to modify oral absorption. Formulation approaches are being explored to enhance bioavailability of poorly water-soluble drugs. One such approach that has been shown significantly enhanced absorption of such drugs is to formulate solid dispersionand then formulate its tablets. Solid dispersion technology can be used to improve the in- vitro and in- vivo dissolution properties of slightly water soluble drugs and to control their dissolution rate. In this current study attempts have been made to formulate sustained release tablets of solid dispersions.

  • FORMULATION AND CHARACTERIZATION OF THEOPHYLLINE MICROSPHERE

    About Authors:
    Sofiya Verma*, Dipak V, Ashok A, Neha C, Jagruti R, Ashutosh. M
    Shri ram institute of pharmacy
    Jabalpur M.P
    *sofiyavermamph@gmail.com

    ABSTRACT:
    The purpose of this research was to prepare and characterize theophylline microsphere of guar gum polymer for the application of nocturnal asthma. The microsphere were prepared by using emulsification method using sodium borate as a cross linking agent and coating was done by solvent evaporation method with the pH sensitive eudragit S-100 polymers. The prepared microsphere were white, free flowing and spherical in shape. The drug-loaded microsphere showed entrapment efficiency and   drug release was extended upto 6 to 8 h. The infrared spectra, differential scanning calorimetry thermographs and XRD spectra all showed the stable character of both the drugs in the drug-loaded microspheres and revealed the absence of drug-polymer interactions. Scanning electron microscopy study revealed that the microspheres were spherical and porous in nature. The prepared theopylline microsphere has the potential for delaying the release of drug.

  • Biosensor for HIV Diagnosis at All Stages of Infection- A Nano Idea

    About Authors:
    Dhanya V C
    Kasturba medical college, Manipal University
    Indian Veterinary Research Institute
    dhanya285@gmail.com

    INTRODUCTION:
    A biosensor is a device that uses specific biochemical reactions mediated by isolated enzymes, immunosystems, tissues, organelles or whole cells to detect chemical compounds usually by electrical, thermal or optical signals (1). Or in other words, Sensor that integrates a biological element with a physiochemical transducer to produce an electronic signal proportional to a single analyte which is then conveyed to a detector.

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  • QUALITY CONTROL TESTING OF PACKAGING MATERIALS

    About Author:
    Sahil Jasuja1*, Mahesh Kumar Kataria2
    1Department of Quality Assurance,
    2Assistant Professor
    Seth G.L. Bihani S.D. College of Technical education (Institute of Pharmaceutical Sciences & Drug Research),
    Sri Ganganagar, (Raj.), India.
    *sahiljasuja@rediffmail.com

  • SMEDDS A NOVEL APPROACH TO IMPROVE BIOAVAILABILITY: A REVIEW

    About Authors:
    Anoop Patel*1, Anoop Kumar1, Neha Sharma1, Monika Prajapati2
    1Department of Pharmaceutical Technology, Meerut Institute of Engineering and Technology, Meerut, U.P., India
    2Raj Kumar Goel institute of technology, 5th K.M. Stone Delhi Meerut Road, Ghaziabad, Uttar Pradesh- 201003
    *anoop.p.2007@gmail.com

    ABSTRACT:
    Oral route still remains the favorite route of drug administration in many diseases because it is very suitable for drug delivery and non invasive. Till today it attracts to many researchers for investigation in the development of new dosage forms. The major problem in oral drug formulations is low and erratic bio-availability due to less water solubility and permeability of the drug across the biological membrane. This may arise high inter and intra subject variability due to lack of dose proportionality and therapeutic failure. It is estimated that 40% of new active constituents which are investigated recently show poor water solubility due to their lipophilic nature. The improvement of bio-availability of these drugs with such properties presents one of the greatest challenges in drug formulations. Several technologies are used for overcome these problems including micronization, solid dispersions, cyclodextrins complex formation and different lipid based drug delivery systems. Self-emulsifying drug delivery system is one the most important and advanced technology for enhancing the oral bio-availability as well reducing in dose. This system also gained attraction for enabling more consistent drug absorption, selective targeting of drugs in GIT, and protection of drugs from the inner environment of gut.

  • BIOPHARMACEUTICAL ANALYSIS NEED AND PROCESS INVOLVED IN PRELIMINARY TREATMENT OF BIOLOGICAL SAMPLES FOR USING LIQUID CHROMATOGRAPHY COUPLED WITH TANDEM MASS SPECTROSCOPY(LC-MS/MS): A REVIEW

    About Authors:
    *S.B.Muthu Vadivel, R.Suresh Kumar1, A.Tamil Selvan2, R.Suthakaran3
    Department of Pharmaceutical Analysis and Quality Assurance
    Teegala Ram Reddy College of Pharmacy

  • DISCUSSION ON NOVEL VAGINAL DRUG DELIVERY SYSTEMS – A RECENT REVIEW

    About Authors:
    Lohithasu Duppala1*, Anil kumar vadda2
    1GITAM Institute of Pharmacy, GITAM University, Pharmaceutics, visakhapatnam, Andhra Pradesh, India-530045.
    2AVANTHI Institute of pharmaceutical sciences, pharmacology, visakhapatnam, Andhra Pradesh, India-530045.
    1lohithasu@gmail.com, 2anilkumar.vadda@gmail.com

    INTRODUCTION:
    Commonly, the olden days ,vaginal drug delivery systems are used to deliver vaginal infections treatment drugs  and contraceptives.1
    The advantage of intra-vaginal controlled drug administration over conventional/traditional oral administration is the drug absorbed systemically because due to the presence of dense network of blood vessels in vaginal wall The vaginal cavity is also an effective site for the uterine targeting of various therapeutic agents such as terbutaline, progesterone and danazol.2   But now-a-days ,the poorly absorbed oral drugs to be formulated as targeted vaginal drug delivery system to treat vaginal infections. In 1970, the first vaginal ring was used for delivery of medroxyprogesterone acetate for contraception.3 Vaginal drug delivery systems are traditionally used to deliver contraceptive and drugs to treat vaginal infections.

  • REVIEW ON PROSTATE CANCER THERAPY

    About Authors:
    Kambham Venkateswarlu1*, G.Sujatha2
    1Graduate Student
    2Department of Pharmaceutical Chemistry
    Sri Lakshmi Narasimha College of Pharmacy, Palluru,
    Chittoor District, Andhra Pradesh-517132, India.
    *k.v.reddy9441701016@gmail.com

    I. INTRODUCTION
    1.1. WHAT IS PROSTATE CANCER?
    Prostate cancer is the most common type of cancer in men and is the second leading cause of cancer-related deaths in men worldwide. It is a disease of the prostate gland in which malignant cells form in the tissues of the prostate and multiply out of control. These cells often metastasize to other parts of the body, like the rectum, the bladder and especially, the bones and the lymph nodes. It generally arises near the surface of the gland so that it can be diagnosed easily by digital rectal examination (DRE). Depending on the extent of metastasis, the prostate cancer tissue has been graded using the Gleason System into a score of 2 to 10 or into four stages I-IV (or, A-D), indicating the likelihood of spreading of the disease to other parts of the body.


    Although several types of cells are found in the prostate, over 99% of the cancers occur in the gland cells only (cells which make the prostate fluid which is added to the semen). Such type of cancer is termed as adenocarcinoma. The region of prostate gland where the adenocarcinoma is most common is the peripheral zone.  Other types of cancer can also start in the prostate gland, including sarcomas (like leiomyosarcoma and rhabdomyosarcoma), small cell carcinomas, and transitional cell carcinomas, although they are extremely rare. Generally, the cancer grows and spreads very slowly. Early prostate cancer most often causes no symptoms. Sometimes, however there are signs and symptoms very close to those of benign prostatic hyperplasia (BPH).

  • BRUGADA SYNDROME: DIAGNOSIS, ORIGIN, RELATION WITH OTHER SYNDROMES

    About Author:
    Kambham venkateswarlu
    Graduate student
    Sri Lakshmi Narasimha College of Pharmacy, Palluru,
    Chittoor District, Andhra Pradesh-517132, India.
    k.v.reddy9441701016@gmail.com

    ABSTRACT:
    Brugada syndrome is a genetic cause of sudden cardiac arrest characterized by abnormal electrocardiographic (ECG) pattern in the right precordial leads either at rest or after provocation. In this condition, sudden death may occur due to polymorphic ventricular tachycardia or ventricular fibrillation. In approximately 30% of patients, sudden cardiac arrest is the initial clinical manifestation of Brugada syndrome.

  • CROSSOVER DESIGNS AND BIOAVAILABILITY STUDY WITH STATISTICAL ANALYSIS: A REVIEW

    About Authors:
    Bhupender Kumar*, Prof. Sudeep Bhardwaj, Monish Sharma, Ramchandra
    Seth G.L. Bihani S.D. College of Technical Education (Institute Of Pharmaceutical Sciences
    And Drug Research), Sri Ganganagar, Rajasthan, 335001
    *bhupendra.nimiwal@gmail.com

    ABSTRACT:
    In a typical crossover design, each subject takes each of the treatments under investigation on different occasions. Comparative bioavailability or bioequivalence studies, in which two or more formulations of the same drug are compared, are usually designed as crossover studies. Perhaps the greatest appeal of the crossover design is that each patient acts as his or her own control. This feature allows for the direct comparison of treatments, and is particularly efficient in the presence of large inter individual variation. However, caution should be used when considering this design in studies where carryover effects or other interactions are anticipated. Under these circumstances, a parallel design may be more appropriate.

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