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Gupta, Shiv Kumar
- Development and Validation of a RP-HPLC Method for Estimation of Thalidomide in Solid Dosage form
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Authors
Affiliations
1 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.), ID
2 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.), IN
3 School of Pharmacy, Galghotia University, Greater Noida, G B Nagar, (U. P.), IN
1 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.), ID
2 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.), IN
3 School of Pharmacy, Galghotia University, Greater Noida, G B Nagar, (U. P.), IN
Source
Asian Journal of Pharmaceutical Analysis, Vol 3, No 1 (2013), Pagination: 17-19Abstract
A simple, rapid and precise isocratic reverse phase High Performance Liquid Chromatographic method has been developed for the determination of Thalidomide capsule. The separation was achieved with 150×4.6mm C18 column using mobile phase as Acetonitrile: Dimethyl Formamide : Water (60:10:30 v/v) at a flow rate of 1.0ml/min with UV detection at 297nm. The retention time of Thalidomide was found to be 2.17min. The linearity range of Thalidomide is 25mg to 200mg with coefficient of correlation 0.9986. The method is found to be accurate, precise and useful in quality control of dosage form.Keywords
RP–HPLC, Thalidomide, Method Development and ValidationReferences
- Mellin GW, Katzenstoin M The Saga of Thalidomide- Neuropathy to Embryopathy, with Case Reports of Congenital Anomalies. New English Journal of Medicine. 267 (23); 1962: 1184-1193.
- Czejka MJ anf Koch HP Determination of thalidomide and its major metabolites by high-performance liquid chromatography. Journal of Chromatography B: Biomedical Sciences and Applications. 413; 1987: 181–187
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- Gorin I Vilette B Gehanno P and Escande JP Thalidomide in hyperalgic pharyngeal ulceration of AIDS. Lancet 335 (8701); 1990: 1343.
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- Radeff B Kuffer R Samson J. Recurrent aphthous ulcer in patient infected with human immunodeficiency virus: successful treatment with thalidomide. Journal of American Acadamy of Dermatol. 23; 1990:523-525.
- Li J Jaworsky MS and Stirling DI The determination of a potential impurity in Thalidomide drug substance and product by HPLC with indirect UV detection. Journal of Pharmaceutical and Bioedical Analysis. 31(1); 2003: 19-27.
- Toraño JS Verbon A Guchelaa HJ Quantitative determination of thalidomide in human serum with high-performance liquid chromatography using protein precipitation with trichloroacetic acid and ultraviolet detection. Journal of Chromatography B: Biomedical Sciences and Applications. 734(2); 1999: 203-210.
- Singh RM Shivraj Mathur SC Singh GN Sharma PK and Gupta SK Method development and its validation of Drug Thalidomide in API usinf RP-HPLC method. Journal of Indian Council of Chemist. 22(2); 2006: 25-27.
- Singh S Singh UK Singh RM Singh GN Mathur SC Saini PK Yadav A Gupta V and Duggal D Development and validation of a RP-HPLC method for estimation of prulifloxacin in tablet dosage form. Indian Journal of Pharmaceutical Science. 73(5); 2011: 557.
- Chen TL Vogelsang GB Petty BG Brundrett RB Noe DA Santos GW and Colvin OM Plasma pharmacokinetics and urinary excretion of thalidomide after oral dosing in healthy male volunteers.Drug Metabolism Disposition 17; 1989: 402-405
- Shabir GA (2003) Validation of HPLC methods for pharmaceutical analysis: Understanding the differences and similarities between validation requirements of the U.S. Food and Drug Administration, the U.S. Pharmacopoeia and the International Conference on Harmonization. J Chromatogr A. 987; 57.
- International Conference on Harmonisation, (1996) Guidance for Industry In: Q2B Validation on Analytical Procedures. Methodology Switzerland IFPMA, 1.
- Development and Validation of a Spectrophometric Method for Estimation of Triamcinolone in Solid Dosage form
Abstract Views :429 |
PDF Views:0
Authors
Affiliations
1 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.), IN
2 School of Pharmacy, Galghotia University, Greater Noida, G B Nagar, (U. P.), IN
1 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.), IN
2 School of Pharmacy, Galghotia University, Greater Noida, G B Nagar, (U. P.), IN
Source
Asian Journal of Pharmaceutical Analysis, Vol 3, No 2 (2013), Pagination: 42-43Abstract
The new simple, sensitive, accurate, precise, rapid and economical method was developed for the estimation of Triamicinolone in solid dosage form. Method is based on the absorbance. Triamcinolone maximum is found at 238 nm in methanol water solvent. The linearity was obtained in the concentration range of 3-9 mcg/ml with coefficient of correlation 0.9998. The value of ruggedness and robustness was found to be 0.2182 and 0.43 respectively. The method is found to be accurate, precise and useful in quality control of dosage form.Keywords
Triamcinolone, Spectrophotometric and ValidationReferences
- Paganelli F Cardillo JA Oliveira AG Melo Jr LAS Skaf M Costa RA A single intraoperative sub–Tenon’s capsule triamcinolone acetonide injection for the treatment of post– cataract surgery inflammation. Ophthalmology 111;2004:2102-8.
- Cardillo JA Melo Jr LAS Costa RA Skaf M Belfort Jr R Souza- Filho AA Farah ME Kuppermann BD Comparison of intravitreal versus posterior sub-tenon’s capsule injection of triamcinolone acetonide for diffuse diabetic macular edema. Ophthalmology 112; 2005:1557-63.
- Magalhães E Nehemy P Santos DVV Fujji G Nehemy MB Avaliação clínica e incidência de endoftalmite infecciosa e nãoinfecciosa após injeção intravítrea de acetonida de triancinolona. Arq Bras Oftalmol. 69; 2006:791-4.
- Paganelli F, Cardillo JA, Melo Junior LA, Lucena DR, Silva- Júnior AA, Hofling AL, Nguye QD, Kuppermann BD, Belfort Junior R, Oliveira AG, A Single Intraoperative Sub-Tenons Capsule Injection of Triamcinolone and Ciprofloxacin in a Controlled-Release System for Cataract Surgery. Invest Ophthalmol Vis Sci. 50; 2009:3041-7.
- Smith RG Burtner AP Oral side effects of the most frequently prescribed drug. Special Care in Dentistry. 14(3); 1994: 96- 102.
- Aquino GDA Stopilha RT Pedrosa, MFF Santos KSCR Egito EST Oliveira AG Silva-Junior AA Validation of quantitative analysis method for triamcinolone in ternary complexes by UVVis spectrophotometry. Rev Ciênc Farm Básica Application. 32(1); 2011: 35-40
- El-Saharty YS Hassan NY Metwally FH Simultaneous determination of terbinafine HCL and triamcinolone acetonide by UV derivative spectrophotometry and spectrodensitometry. Journal of Pharmacological and Biomedical Analysis 28(3- 4); 2002:569-80.
- Gupta SK Kumar B and Sharma PK Development and validation of a RP-HPLC method for estimation of Thalidomide in solid dosage form. Asian Journal of Pharmaceutical Analysis. 3(1); 2013: 17-19.
- Singh RM Shivraj Mathur SC Singh GN Sharma PK and Gupta SK Method development and its validation of Drug Thalidomide in API using RP-HPLC method. Journal of Indian Council of Chemist. 22(2); 2006: 25-27.
- Singh S Singh UK Singh RM Singh GN Mathur SC Saini PK Yadav A Gupta V and Duggal D Development and validation of a RP-HPLC method for estimation of prulifloxacin in tablet dosage form. Indian Journal of Pharmaceutical Science. 73(5); 2011: 557.
- International Conference on Harmonisation, (1996) Guidance for Industry in: Q2B Validation on Analytical Procedures. Methodology Switzerland IFPMA, 1.
- Spectrophotometric Estimation of Dextromethorphan in Bulk Drug using Hydrotropic Solubilization Technique
Abstract Views :945 |
PDF Views:1
Authors
Affiliations
1 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.), IN
1 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.), IN
Source
Asian Journal of Pharmaceutical Analysis, Vol 3, No 3 (2013), Pagination: 90-93Abstract
A simple, rapid and precise spectrophotometric method has been developed for determining the enhancement in the aqueous solubility Dextromethorphan. Method is based on the absorbance. Dextromethorphan maximum is found at 278nm with hydrotrope dextromethorphan in double distilled water as solvent. The linearity was obtained in the concentration range of 10-120μg/ml with coefficient of correlation 0.9993.The % RSD in case of intra-day and inter day was found to be 0.8182 and 0.9438 respectively. The value of LOD and LOQ was found to be 3.76 and 1.141 respectively. The method is found to be accurate, precise and useful in quality control of API Drug and also to enhance the aqueous solubility of Dextromethorphan.Keywords
Dextromethorphan, Hydrotropic Study, Enhancement of Solubility, Method Development and ValidationReferences
- Li P Zhao L, Developing early formulations: Practice and perspective. International Journal of Pharmaceutics 341(1-2); 2007:1-19.
- C. Neuberg, Biochem Z., 1916, 76: 107.
- Cui Y Parallel stacking of caffeine with riboflavin in aqueous solutions: The potential mechanism for hydrotropic solubilization of riboflavin. International Journal of Pharmaceutics 15 397(1-2); 2010:36-43.
- Jain N Jain R Jain A Pandey SP Jain DK Spectrophotometric quantitative estimation of amlodipine besylate in bulk drug and their dosage forms by using hydrotropic agent. Eurasian J. Anal. Chem. 5; 2010: 212-217.
- Pandey S Maheshwari RK A novel Spectroscopic Method for the estimation of Ketoprofen in tablet dosage form using hydrotropic solubilization phenomenon. World Applied Sciences Journal 11; 2010:1524 - 1527.
- Maheshwari RK Indurkhya A Novel application of mixed hydrotropic solubilization technique in the formulation and evaluation of hydrotropic solid dispersion of aceclofenac. Asian Journal of Pharmaceutics 4; 2010: 235 - 238.
- Vemula VR Lagishetty V Lingala S Solubility enhancement techniques. Int. J. Pharm. Sci., Review and Research 5 (1); 2010: 41-51.
- Saravanakumar G Choi KY Yoon HY Kim K Park JH Kwon IC Park K Hydrotropic hyaluronic acid conjugates: Synthesis, characterization, and implications as a carrier of paclitaxel. International Journal of Pharmaceutics 394; 2010: 154-161.
- Baghel US Dhiman V. Exploring the Application of Hydrotropic Solubilization Phenomenon for Estimating Diacerein in Capsule Dosage Form by Spectrophotometry Methods. Asian Pacific Journal of Tropical Biomedicine. 2010: S1720-S1727.
- Maheshwari RK, Lakkadwala S, Vyas R, Ghode P. Spectrophotometric determination of naproxen tablets using niacinamide as hydrotropic solubilizing additive. Journal of Current Pharmaceutical Research4; 2010: 11-14.
- Maheshwari RK Bishnoi SR Kumar D Murali K. Digest Journal of Nanomaterials and Biostructures.5; 2010:97-100.
- Maheswari RK Chandrawashi H, Gupta N, Quantitative estimation of aspirin in tablets and bulk sample using metformin hydrochloride as hydrotropic agent. International Journal of Pharmacy and Pharmaceutical Sciences 2010, 2, 21-23.
- Maheshwari RK Archana A, Amit R, Megha A. Ecofriendly spectrophotometric estimation of atenolol tablets using metformin hydrochloride as hydrotropic solubilizing agent. Journal of Global Pharma Technology. 2; 2010: 93-96
- Jayakumar C, Kumar DK, Nesakumar D, Gandhi NN. Quantitative analysis of theophylline bulk sample using sodium salicylate hydrotrope. International Journal of Pharmacy and Pharmaceutical Sciences 2; 2010:124-125.
- Sherje AP, Anand R, Sriram W, Vanshiv SD. Mixed hydrotropy in spectrophotometric analysis of nitazoxanide. International Journal of Chem. Tech. Research 2; 2010: 1966-1969.
- Maheshwari RK, Rajput MS, Sinha S. New quantitative estimation of benzoic acid bulk sample using calcium disodium edetate as hydrotropic solubilizing agent. Asian Journal of Pharmaceutical and Clinical Research 3; 2010: 43-45.
- Sharma MC, Sharma S. Spectrophotometric determination of Lamivudine in Bulk and Pharmaceutical Formulation using hydrotropic Solubilization. Int. J. Pharm Tech Research3; 2011:988-991.
- Fabregas JL, Margalet A. GLC trace analysis of Dextromethorphan and bromhexine salts in pharmaceutical preparations. Journal of Pharmaceutical Sciences. 64(6); 1975: 1005-1006
- International Conference on Harmonization, (2005) Guidance for Industry in: Q2B Validation on Analytical Procedures. Methodology Switzerland IFPMA, 1.
- Study on Taste Masking of Ranitidine HCl Using Ion Exchange Resin
Abstract Views :401 |
PDF Views:2
Authors
Affiliations
1 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.), IN
2 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.) India, IN
3 School of Pharmacy, Galghotia University, Greater Noida, G B Nagar, (U. P.), IN
1 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.), IN
2 College of Pharmacy, Shree Ganpati Institute of Technology, NH-24, Opp. Jindal Pipes Ltd, Ghaziabad, (U.P.) India, IN
3 School of Pharmacy, Galghotia University, Greater Noida, G B Nagar, (U. P.), IN
Source
Asian Journal of Pharmacy and Technology, Vol 3, No 2 (2013), Pagination: 60-62Abstract
The taste of a drug plays an important role in patient compliance. Ranitidine HCl is a Histamine blocker drug with bitter taste. The drug Ranitidine HCl was treated with a cation exchange resin, which forms complex with the drug and mask the bitterness of Ranitidine HCl. The loading process was optimized for the resin type, pH of loading solution and drug:resin ratio. The resin-drug complex was evaluated for taste by panel method. The rate of dissolution was studied and the drug had showed good release. These findings can be utilized to formulate a non bitter dosage form for Ranitidine HCl with good bioavailability.Keywords
Ranitidine HCl, Ion Exchange Resin, Taste Masking, ResinatesReferences
- Dorfner K, Ion Excahanger properties and applications, 3rd edition, Ann Arbor Science Publisher 1972.
- Borodkin S and Sandberg DP, Chewable tablets including coated particles of pseudo-ephedrine-weak cation exchange resin, Patent US, , 3, 594; 1972: 740.
- Long C, Biochemist Hand book, D. Van Nostrand, Princeton, N J, 1961: 909.
- Honeysett RA (GB), Taste masked buflomedil preparations, European Patent Appl, EP, 1992: 0501763.
- Lange, Preparation and use of ion exchange resins loaded with quinolonecarboxylic acid derivatives, Patent US, 3, 152; 1992: 986.
- Avari JG and Bhalekar M, Cation exchange resins for taste masking and rapid dissolution of Sparfloxacin, Indian Drugs, 41(1); 2004:19-23.
- Borodkin S Encyclopedia of Pharmaceutical Technology, 12th edition, Marcel Decker Inc., N. Y., 1996: 207.
- Borodkin S and Sandberg DP Polycarboxylic acid ion-exchange resin adsorbates for taste coverage in chewable tablets. Journal of Pharmaceutical Sciences, 60; 1971: 1523.
- A Comparative Study of Mobile Wireless Networks
Abstract Views :283 |
PDF Views:2
Authors
Affiliations
1 School of Engineering and Technology, Jaipur National University, Jaipur, IN
2 Department of Computer Science and Electronics, Bansthali University, Rajasthan, IN
1 School of Engineering and Technology, Jaipur National University, Jaipur, IN
2 Department of Computer Science and Electronics, Bansthali University, Rajasthan, IN
Source
Oriental Journal of Computer Science and Technology, Vol 4, No 2 (2011), Pagination: 387-392Abstract
As the coming generation is going to be the mobile communication technology Generation. If we talk about the communication, at present we are fully equipped with 2G and have started using 3G. But time is not so far when we deal with 4G and it's beyond mobile communication technology. In this paper we have just tried to present the brief overview and limitations of existing systems and how generation next mobile communication technology is going to start new evolution. The G Next revolution, we call it 4G. In this I have discuss the overview, features of 4G, its future vision and scope. This paper will help the new scholars to enhance their knowledge about the different mobile communication existing and G Next systems.Keywords
FDMA, TDMA, CDMA, GSM, OFDM, WiMax.- Role of Metadata in Data Warehousing for Effective Business Support
Abstract Views :137 |
PDF Views:2
Authors
Affiliations
1 School of Engineering and Technology, Jaipur National University, Jaipur, IN
2 Department of Computer Science and Electronics, Banasthali University, Rajasthan, IN
1 School of Engineering and Technology, Jaipur National University, Jaipur, IN
2 Department of Computer Science and Electronics, Banasthali University, Rajasthan, IN
Source
Oriental Journal of Computer Science and Technology, Vol 4, No 2 (2011), Pagination: 435-438Abstract
Today large organizations are being served by different types of area processing and information systems. It is important to create an integrated repository of what these system contain and do it in order to use them collectively and effectively. The repository contains metadata of source systems effectively. The repository contains metadata of source systems data warehouse and also business data. Metadata, usually called data about data, is an important part. Metadata is supposed to be a helping hand to all co-workers in an organization that work directly or indirectly with the data warehouse. The main purpose of this paper is to determine through feedback from the business end user.
Keywords
Metadata, DSS, DW, ETL, OLAP.- Chemical Analysis Case Study of Underground Water in Hapur (West)
Abstract Views :280 |
PDF Views:5
Authors
Affiliations
1 Sanskar College of Pharmacy and Research, Opp. Jindal Pipes Ltd., NH-24, Ghaziabad (U.P.) 201302, IN
1 Sanskar College of Pharmacy and Research, Opp. Jindal Pipes Ltd., NH-24, Ghaziabad (U.P.) 201302, IN
Source
Asian Journal of Pharmaceutical Analysis, Vol 7, No 2 (2017), Pagination: 113-116Abstract
Underground water contamination is a kind of water pollution or water destruction, in which various contaminants unify together to degrade quality and nature of water. Present scenario most probably support the water contamination by the humans and up to less extent by the natural disasters. The major ions which are responsible to maintain the quality of ground water are carbonate (CO3 2-) and bicarbonate (HCO3 -), Chloride (Cl), Sulphate (SO4 --), Nitrate (NO3 --), Phosphate (PO4 3-), and Fluoride (F-). The above ions are present in the form of anions. These anions are in general maintain by the cations as Ca++,Cu++, Mg++, Na+, and K+. Among the above briefed ions Ca++ and Mg++ are the ones which are responsible for the hardness of the water. These are found abundantly in the area, where manufacturing of chalk and limestone works take place. Water's hardness is determined by the concentration of multivalent cations in the water. This hard water if consumed by animals or humans lead to the terrific pathological conditions. Three water samples are collected from different locations of Pilkhuwa, District Hapur near to the location of the industry with limestone works, during summer. The ionic concentrations are expressed in mg/L.Keywords
Ground Water Quality, Total Alkalinity, Total Hardness, Electrical Conductivity, TDS.- Chemical Analysis of Underground Drinking Water Quality in Ghaziabad
Abstract Views :253 |
PDF Views:1
Authors
Affiliations
1 Sanskar College of Pharmacy and Research, Opp. Jindal Pipes Ltd., NH-24, Ghaziabad (U.P.) 201302, IN
1 Sanskar College of Pharmacy and Research, Opp. Jindal Pipes Ltd., NH-24, Ghaziabad (U.P.) 201302, IN