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  • REVIEW ON THE LEAD OPTIMIZATION TECHNIQUES (PHASE-I)

    About Authors:
    Kambham Venkateswarlu*, D.Z.Suhasini
    Department of Pharmacology,
    Sri Lakshmi Narasimha College of Pharmacy (JNTUA), Pallur,
    Chittoor, Andhra Pradesh, India.
    *k.v.reddy9441701016@gmail.com

    ABSTRACT:
    Lead optimization techniques are deals that new discovery is to choose the compounds with a known pharmacological action and proceed to modify the molecular structure of the compound systemically to get a drug with desired properties pharmacological action and pharmacokinetics. The compounds of the drugs are choosing for the study is called as lead.

    Generally the identification and synthesis of compounds which are structurally related to the lead compound and testing their pharmacological activity. In the process it is possible to find a better drug than the lead compound.

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  • STABILITY-INDICATING RP- HPLC METHOD FOR ANALYSIS OF SITAGLIPTIN IN THE BULK DRUG AND IT’S PHARMACEUTICAL DOSAGE FORM

    About Authors:
    V.DEEPTHI *, POORNIMA.Y, DR.G.DEVALA RAO, T.SANDEEP REDDY
    Department of Pharmaceutical Analysis,
    K.V.S.R.Siddharthacollege of pharmaceutical sciences,
    Vijayawada-520010, India.
    *deepthi759@gmail.com

    ABSTRACT
    A novel stability-indicating RP-HPLC method has been develop and validated for quantitative analysis of Sitagliptin in the bulk drug and in its pharmaceutical dosage forms using Hypersil–BDS- C18 column (250x4.6mmi.d, 5µ particle size) with 10mM Phosphate buffer (PH-3.5): ACN 60:40%v/v as isocratic mobile phase enabled separation of the drug from its degradation products. UV detection was performed at 260 nm. The method was validated for linearity, accuracy (recovery), precision, sensitivity, ruggedness and robustness. The linearity of the method was excellent over the range 10–60μg/ml (correlation coefficient 0.999). The limits of detection and quantification were 0.21 and 0.640μg/ml, respectively. Recovery of Sitagliptinfrom the pharmaceutical dosage form ranged from 99.99 to 100.05%.

    Sitagliptin was subjected to stress conditions (Hydrolysis (acid, base), oxidation,thermal and photo degradation) and the stressed samples were analysed by use of the method. Degradation was observed in acid, base, and 30% H2O2. The drug was stable under the other stress conditions investigated. The degradation products were well resolved from main peak. The forced degradation studies prove the stability indicating power of the method.

  • PYRROLE, FURAN, THIOPHENE DERIVATIVES & PHARMACOLOGICAL ACTIVITIES: A REVIEW

    About Authors:
    C.P.Meher*, S.P.Sethy, M.Madhavi
    *Asst. Professor
    Maheshwara Institute of  Pharmacy,
    Chitkul, Patancheru, Medak, A.P
    *chaitanyameher84@gmail.com

    ABSTRACT:
    Medicinal chemistry and pharmaceutical chemistry are disciplines at the intersection of chemistry, especially synthetic organic chemistry, and pharmacology and various other biological specialties, where they are involved with design, chemical synthesis and development for market of pharmaceutical agents, or bio-active molecules (drugs).Very important part of above is the heterocyclic-chemistry. Now a days so many investigation are carried out for developing new chemical entities having suitability for human life. A lot of research work is going on presently for development of new heterocyclic derivatives.The present review article is concern with the three, five-membered heterocyclic compound pyrrole, furan & thiophene  derivatives that show diverse pharmacological activities.

  • PHYSICAL STABILITY TESTING OF DRUGS AND DRUG PRODUCTS

    About Authors:
    L.D.Budania
    Seth G. L. Bihani S. D. College Of Technical Education,
    Institute Of Pharmaceutical Sciences & Drug Research, Gaganpath,
    Sri Ganganagar, Rajasthan 335001
    *ldbudania@gmail.com

    ABSTRACT:
    Stability is an essential quality attribute for drug products. If there is any functionally relevant quality attribute of a drug product that changes with time, this evaluation checked by pharmaceutical scientist and regulators who quantify drug product stability and shelf life. The rate at which drug products degrade varies dramatically. E.g. radiopharmaceutical products. Since the evaluation of the stability of drug is highly specialized and esoteric nature. Drug stability concerns about drug product safety, efficacy, and quality, found it to appropriate. Stability studies are done through the regulatory agencies such as FDA and HPB (health protection branch).

  • EFFECT OF PRUNUS AMYGDALUS (BATSCH) IN DIFFERENT MODELS OF ULCER

    About Authors:
    Devendra Kumar1,Pragya Seth2
    Department of Pharmaceutical technology,
    1Sri Satya Sai collage of Pharmacy Bhopal,
    2Lakshmi Narain College of Pharmacy, Bhopal
    *guptadevendra15@gmail.com

    Abstract
    The present work describes the effect of methanolic extract of Prunus amygdalus (batsch.) on pylorus ligation and Ethanol-induced gastric ulcer models in Wistar rats. The present study provides a strong evidence of antiulcer activity of Prunus amygdalus extract against gastric lesions. The antiulcer activity is recognized by a reduction in acid-secretary parameters like total and free acidity, gastric volume and ulcer score suggesting that acid inhibition accelerates ulcer healing, thereby strengthening of mucosal barrier. In this present study it shows significant protection for Hexosamine in all treated groups in comparison to negative control group. Inthe LPO results it was observed that there was significance level difference in negative control group and all other group that indicates that lipid peroxides enzyme was higher in vehicle treated group. Ulcer score was determined by the counting of spots and severity of damage in stomach part by any moiety such as ethanol. Single drug treatment (200 mg/kg and 400mg/kg of P.A.E.) was effective up to a significant level (P<0.05) in compare to negative control group.Volume of gastric juice indicate the secretions of gastric fluid and it is higher in negative control group and all drug treated group was effective in relation to negative control group in significance level (P <0.05).

  • MANUFACTURING DOCUMENTATION IN PHARMACEUTICAL INDUSTRY- DEVELOPMENT AND IMPLEMENTATION

    About Authors:
    Krunal Parikh1*, Mr. Maheshkumar Kataria2, Jatin Patel1
    2Assistant professor, Department of pharmaceutics,
    1Seth G.L. Bihani S.D. College of Technical Education,
    Institute of Pharmaceutical Sciences and Drug Research,
    Sri Ganganagar, Rajasthan, INDIA
    *Krunal_2922@yahoo.in

    ABSTRACT
    Documentation is an integral part of good manufacturing practices. It defines a system of information and control so that risks so inherent in misinterpretation and/or error in oral communication are minimized. It consequently strengthens the quality, and its consistency, of all goods and services, as those responsible for the specific operations have clear, unambiguous instructions to follow including active drug substances, is legally mandatory.

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  • NANOTECHNOLOGY IN MEDICINE

    About Authors:
    P.Ramanujaiah*, Dr M.Purushothaman, Hemalatha
    Vasavi institute of pharmaceutical sciences, Kadapa
    *rama.mpharm@gmail.com

    Abstract:
    The application of nanotechnology to drug delivery has currently more than 20 Nanoparticles therapeutics are in clinical use, validating the ability of Nanoparticles to improve the therapeutic index of drugs. In addition to the already approved Nanoparticles, numerous other Nanoparticles platforms are currently under various stages of preclinical and clinical development, including various liposomes, polymeric micelles, dendrimers, quantum dots, gold Nanoparticles, and ceramic Nanoparticles. With continued research and development efforts, nanotechnology is expected to have a tremendous impact on medicine for decades to come.

  • ROLE OF CHROMATOGRAPHY IN EVALUATION OF HERBAL DRUGS: A SHORT REVIEW

    About Author:
    Alimuddin Saifi
    N.K.B.R. College of Pharmacy & Research Centre,
    Meerut
    asaifi2005@gmail.com

    Abstract
    Herbal drugs are accepted as important therapeutic agents for the treatment of many diseases. The development of authentic analytical methods which can reliably profile the phytochemical composition, including quantitative analyses of marker/bioactive compounds and other major constituents, is a major challenge to scientists. Pharmacognostical analysis of medicinal herbs remain challenging issues for analytical chemists, as herbs are a complicated system of mixtures. Analytical separation techniques for example high performance liquid chromatography (HPLC), gas chromatography (GC) and mass spectrometry (MS), High Performance Thin Layer Chromatography (HPTLC) etc. among the most popular methods of choice used for quality control of raw material and finished herbal product.

  • MASTER PIECE FOR METABOLIC PATHWAYS : THE ENZYME

    About Authors:
    *C.P. Meher,  S.P.Sethy, B.Pochaiah
    Department of pharmaceutical Bio-Chemistry,
    Maheshwara college of Pharmacy, chitkul (V),
    Isnapur “X” Road,  patancheru, Hyderabad.
    *chaitanyameher84@gmail.com

    ABSTRACT :-
    “Enzyme are the catalyst of the living world ! protein in nature, and in action in specific ,rapid and accurate; huge in size but with small active centers; highly exploited for disease diagnosis in lab centers”[1] Enzyme promotes & control the conversion of the complex carbohydrates, fats & protein of our body into simple substances which the intestine can absorb & also the various reaction by which these simple substances are used in the body for building up new tissue  or producing energy. The enzyme are not broken down or changed in the process . they are as potent at the end of the reaction at the beginning & very small amounts can effect the conversion of large quantity of material . they are the true catalyst.[2] They are actively take part in every metabolic pathways that occur in our body. This review is concern with comparative study of the various enzyme related with various metabolic pathways as well as the drugs associated for inhibition to give respective pharmacological responses.

  • STUDIES ON THE THERAPEUTIC ROLE OF VITAMIN B12 AND FOLIC ACID AGAINST ARSENIC INDUCED HEPATIC DAMAGES AT CELLULAR AND DNA LEVEL BY REACTIVE OXYGEN SPECIES

    About Authors:
    Tamal maity
    Institute of pharmacy ,(govt.) ,
    Jalpaiguri and west bengal university of health sciences
    Vidyasagar University
    tamalpharma@gmail.com

    Abstract:
    In an attempt to develop new therapeutics, Vitamin B12 & Folic acid was used to screen the effect on arsenic-induced hepatic toxicity in female rat of Wistar strain. Sub chronic exposure to sodium arsenite (0.4 ppm/100 g body weight/day via drinking water for a period of 28 days) significantly increased activities of hepatic. A notable distortion of hepatocellular histoarchitecture was prominent with a concomitant increase in DNA fragmentation following arsenic exposure. A marked elevation of in hepatic tissue was also evident from the hepatic accumulation of antioxidant enzymes such as superoxide dismutase, Catalase, Xanthine Oxidase, DNA Fragmentation & Histological views. However, co-administration of Vitamin B12 & folic acid (200 µl/100 g body weight/day for a period of 28 days) was found to significantly prevent the arsenic-induced alteration of hepatic function. Moreover, the degeneration of histoarchitecture of liver found in arsenic-treated rats was protected along with partial but definite prevention against DNA fragmentation induction. Similarly, generation of reactive oxygen species and free radicals were found to be significantly less along with restored activities of antioxidant like Vitamin B12 & Folic acid co-administered group with comparison to arsenic alone treatment group. The present investigation offers strong evidence for the hepato-protective and antioxidative efficiencies of Vitamin B12 & Folic acid against oxidative stress induced by arsenic.

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