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  • ALCOHOL IS SAFE OR DANGEROUS, IS A BIG QUESTION MARK OR WE CAN SAY IT’S A ‘WH’ TYPE QUESTION

    Alcohol means ethyl alcohol are hydroxyl derivatives of aliphatic hydrocarbons. Production of alcohol needs only a few basic ingredients., these are sugar, water, yeast and a warm atmosphere. Alcohol is prepared by the fermentation process by means fermentation of sugar.

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  • ROLE OF PURPLE CORN IN TREATMENT OF TYPE 2 DIABETES AND KIDNEY DISEASE: A THERAPEUTIC REVIEW

    About Authors:
    Mr. Satyanand Tyagi
    President, Tyagi Pharmacy Association & Scientific Writer,
    Chattarpur, New Delhi, India.
    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 50 Publications (42 Review Articles and 08 Research Articles of Pharmaceutical, Medicinal and Clinical Importance, published in standard and reputed National and International Pharmacy journals; Out of 50 publications, 11 are International Publications).
    sntyagi9@yahoo.com,
    +91-9871111375 / 9582025220

    ABSTRACT:
    Diabetic nephropathy is one of the most serious complications related to diabetes, often leading to end-stage kidney disease. Purple corn grown in Peru and Chile is a relative of blue corn, which is readily available in the U.S. The maize is rich in anthocyanins (also known as flavonoids), which are reported to have anti-diabetic properties. Scientists from the Department of Food and Nutrition and Department of Biochemistry at Hallym University in Korea investigated the cellular and molecular activity of purple corn anthocyanins (PCA) to determine whether and how it affects the development of diabetic nephropathy (DN). Their findings suggest that PCA inhibits multiple pathways involved in the development of DN, which may help in developing therapies aimed at type 2 diabetes and kidney disease. The aim of present article is to provide in depth knowledge about Purple Corn, their clinical and biological utility as well as their role in treatments of type 2 diabetes and kidney disease. An attempt is also made to focus on compounds found in purple corn which may aid in developing future treatments for type 2 Diabetes as well as kidney disease.

  • SOLUBILITY ENHANCEMENT OF POORLY WATER SOLUBLE DRUG CELECOXIB

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    About Authors:
    Mr. Pranab Prakash Panigrahi1*, Mr. Ajit Kumar Acharya2
    1B.Pharm, ROYAL COLLEGE OF PHARMACY AND HEALTH SCIENCES, BERHAMPUR
    2Asst.Professor, ROYAL COLLEGE OF PHARMACY AND HEALTH SCIENCES, BERHAMPUR

    *pranab.panigrahi@rediffmail.com

    INTRODUCTION
    Poorly water-soluble drugs often require high doses in order to reach therapeutic plasma concentrations after oral administration. Improvement in the extent and rate of dissolution is highly desirable for such compounds, as this can lead to an increased and more re-producible oral bioavailability and subsequently to clinically relevant dose reduction and more reliable therapy. More than 40% of newly discovered drugs have little or no water solubility presents a serious challenge to the successful development and commercialization of new drugs in the pharmaceutical industry. Now a days, pharmaceutical technology provides many approaches to enhance the dissolution rate of poorly soluble drugs. Physical modifications often aim to increase the surface area, solubility and/or wet ability of the powder particles and are therefore focused on particle size reduction or generation of amorphous states [Hancock, 1997 & Grau, 2000]. Several methods have been employed to improve the solubility of poorly water soluble drugs. A solid dispersion technique has been used by various researchers who have reported encouraging results with different drugs. The first drug whose rate and extent of absorption was significantly enhanced using the solid dispersion technique was sulfathiazole by Sekiguchi and Obi (Sekiguchi, 1961)1.

  • FORMULATION AND INVITRO EVALUATION OF IMMEDIATE RELEASE FOR QUETIAPINE FUMARATE IN TABLET DOSAGE FORM

    About Authors:
    Ashokkumar.m*, M.Senthil kumar, Dinesh, Jenish, Marshel, Hariharan
    Annai veilankanni’s college of pharmacy
    Saidapet, Chennai-600015, Tamilnadu
    *mgashokkumar123@gmail.com

    ABSTRACT
    Atypical antipsychotic Quetiapine was used for the treatment of schizophrenia is a severe illness with substantial effects on individual and social functioning, Quetiapine and its active metabolite N-desalkyl-Quetiapine have affinities to dopaminergic D1-and D2receptors,5-HT2 receptors. To design of immediate release dosage form of quetiapine fumarate that will help in releasing drug with short period of time. The quetiapine fumarate tablets were successfully prepared by direct compression method. The physiochemical evaluation results for the powdered material of all trials pass the official limits in angle of repose, compressibility index and drug content. In the 9 trials, the optimized formulation was F3 trial which releases the quetiapine fumarate  immediately within an hour.

  • 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.

  • SCREENING OF DIURETIC AGENTS-AN OVERVIEW

    About Authors:
    *Nilesh Sovasia, Prof.Sanjeev Thacker, Arshad Hala
    Seth G.L.Bihani S.D.College Of Technical Education,
    Institute Of Pharmaceutical Science & Drug Research,
    Sri Ganganagar,Rajasthan,India
    *nilesh.sovasia@yahoo.com

    ABSTRACT
    Diuretic agents are very useful for several critical conditions like hypertension, heart failure, renal failure, nephrotic syndrome, and cirrhosis.The various methods for screening of Diuretic agents provides useful tool to evaluate the safety and effectiveness of the drugs.It is also useful for determining the dose lavel of particular class of diuretic agents.

  • UV- SPECTROPHOTOMETRIC METHOD DEVELOPMENT FOR THE DETERMENATION OF PARACETAMOL AND DROTAVERINE HYDROCHLORIDE IN COMBINATION TABLET DOSAGE FORM BY SIMULTANEOUS EQUATIONS METHOD

    About Authors:
    Rambabu.CH*, V. V. V. S. P. Apparao, Miss. M.  Muthulakshmi, V. Ananth.
    aPG-Student, Department Of Pharmaceutical Analysis,
    KMCH College of Pharmacy,
    Kalapatti Road, Coimbatore– 641 048, INDIA.
    *ramgepharma@gmail.com

    ABSTRACT:
    At present, simultaneous determination of drugs in the combination dosage forms has been enjoying renaissance in the field of pharmaceutical analysis. Paracetamol, a classical antipyretic in combination with a novel antispasmodic drug, drotaverine hydrochloride provides a synergistic effect in the treatment of spasms. From the reviewed literature, it was simultaneous uv-spectrophotometric methods have not yet been developed for the determination and quantification of paracetamol and drotaverine hydrochloride. The λmax of paracetamol is 257 nm and that of drotaverine hydrochloride were scanned and found to be 308 nm, 352 nm. Both paracetamol and drotaverine hydrochloride were found to have significant absorbance of the λmax   of each other and total absorbance was equal to the sum of the absorbance of paracetamol and drotaverine hydrochloride individually measured. So the present study involves the uv-spectrophotometric method development for the simultaneous determination of paracetamol and drotaverine hydrochloride by using simultaneous equations method. The mean % recoveries from this method were found to be 100.76% and 100.17% for paracetamol and drotaverine hydrochloride respectively proving that the method is accurate.

  • ESTIMATION OF TEMOZOLOMIDE BY USING RP-HPLC IN ITS PHARMACEUTICAL DOSAGE FORM

    About Authors:
    Segu Sairam*, Mulla Mahaboob Basha, S Ananda Thangadurai, V Kranthi kumar
    Swamy vivekanandha college of pharmacy, dept. Of pharmaceutical analysis,
    Elayampalayam, tiruchengode – 637205.
    *Sairampharma2020@gmail.com

    ABSTRACT
    A simple, sensitive and specific method reverse phase - high performance liquid chromatography (RP-HPLC) have been developed and validated for the estimation of Temozolomide in its Pharmaceutical dosage form.
    Estimation of Temozolomide by using RP-HPLC coupled with UV

    An isocraticREVERSE PHASE - HIGH PERFORMANCE LIQUID CHROMATOGRAPHY method was developed and validated for the estimation of Temozolomide in its Pharmaceutical dosage forms. The separation of the analytes was performed on aDevelosil ODS MG.5 (150×4.6mm),5µm, with mobile phase containing (0.5% w/v glacial acetic acid) named as Solution-A  :  Methanol  [90 : 10, v / v] was used. The flow rate was 1 ml min-1 and separation was monitored by UV detection at 254 nm. Chromatogram showed peak at a retention time of 7.306 ± 0.009 min. validation of the method for linearity and range, intra-day and inter-day precision, accuracy, specificity, recovery, ruggedness, robustness and limits of detection and quantification were obtained as 0.598 µg / ml and 1.81 µg / ml respectively. The calibration plot was linear from 20-60 µg ml-1 and the correlation coefficient was 0.999.The proposed method is fast, accurate and precise for the quantitative determination of Temozolomide capsules.

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  • ROLE OF ERLOTINIB IN NON-SMALL CELL LUNG CANCER AS WELL AS PANCREATIC CANCER: A REVIEW

    About Authors:
    Satyanand Tyagi*
    *President, Tyagi Pharmacy Association & Scientific Writer,
    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 49 Publications (41 Review Articles and 08 Research Articles of Pharmaceutical, Medicinal and Clinical Importance, published in standard and reputed National and International Pharmacy journals; Out of 49 publications, 11 are International Publications).
    *sntyagi9@yahoo.com
    , +91-9871111375 / 9582025220

    ABSTRACT:
    Erlotinib is a drug used to treat non-small cell lung cancer, pancreatic cancer and several other types of cancer. It is a reversible tyrosine kinase inhibitor, which acts on the epidermal growth factor receptor (EGFR). It is marketed in the United States by Genentech and OSI Pharmaceuticals and elsewhere by Roche. In lung cancer, it extends life by an average of 3.3 months at a cost of CDN $ 95,000. The hydrochloride salt of a quinazoline derivative of the drug shows antineoplastic properties. Competing with adenosine triphosphate, erlotinib reversibly binds to the intracellular catalytic domain of epidermal growth factor receptor (EGFR) tyrosine kinase, thereby reversibly inhibiting EGFR phosphorylation and blocking the signal transduction events and tumorigenic effects associated with EGFR activation. Erlotinib hydrochloride is approved to be used alone or with other drugs to treat:
    * Non-small cell lung cancer that is locally advanced or has metastasized (spread to other parts of the body). It is used in patients who have already been treated with other chemotherapy.
    * Pancreatic cancer. It is used with gemcitabine hydrochloride in patients whose disease cannot be removed by surgery or has metastasized.

    Erlotinib hydrochloride is also being studied in the treatment of other types of cancer. The aim of present article is to provide in depth knowledge about the drug Erlotinib as well as its role in treatment of non-small cell lung cancer as well as pancreatic cancer.The review has also focused about chemistry, pharmacology as well as clinical trial studies of the Erlotinib.

  • Pharmacological Screening of Ethanolic Extract of Plant Solanum XanthocarpumOn Nephrolithiasis Rats

    About Authors:
    Amar Patil*, Shraddha Kanase
    M.Pharm (Pharmacology)    
    Department Of Pharmacology, Tatyasaheb Kore College Of Pharmacy,
    Warananagar. Dist;Kolhapur, India .
    *appatil.tkcp@gmail.com

    Abstract:
    Solanum Xanthocarpumhas been known traditionally in Indian system of medicine for the treatment of various metabolic disease and disorders. Since, the present study was carried out to know its applicability in urolithiasis condition. In the present study, extracts of Solanum Xanthocarpumwas prepared with Ethanol and used for evaluation of antiurolithiatic activity. In this study we systematically evaluated its property by using Ethylene Glycol induced Albinorats. This study also involves state of the art animal model to elucidate its probable mechanism of industrial guidelines of FDA, USA for pre-clinical evaluation of anti-Nephrolithiasis drugs.

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