Gotowe bibliografie tematyczne / Colon targeted tablets

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Gotowa bibliografia na temat „Colon targeted tablets”

Autor: Grafiati
Data publikacji: 2 czerwca 2025
Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Colon targeted tablets"

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Dr.Shaikh, Siraj N* Mo. Irfan Mo.Hasnain Dr.G. J. Khan Shoaib Ahmad. "FORMULATION, OPTIMIZATION AND EVALUATION COLON TARGATED DRUG DELIVERY SYSTEM FOR ORNIADAZOLE." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 04 (2018): 3168–76. https://doi.org/10.5281/zenodo.1238402.

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The colon is a site where both local and systemic delivery of drugs can take place. The present investigation concerns with formulation and evaluation of Colon Targeted dip coated tablets of Ornidazole by using HPMCK4 M, Xanthan gum polymers .Initially core tablets were prepared and then coated by using Eudragit S100 as a enteric coating polymer with the help of Isopropyl alcohol, acetone (1:1) by deep coating. Optimization of colon targeted tablet of Ornidazole was carried out by using design expert software considering combination of HPMC K 4 M & Xanthan gum as independent variable &
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Jaiswal, Anamika, Ashok Koshta, Sapna Malviya, and Anil Kharia. "Formulation and Evaluation of Colon Targeted Matrix Tablets of Mesalazine." American Journal Of Pharmacy And Health Research 10, no. 12 (2022): 23–36. https://doi.org/10.5281/zenodo.7479322.

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ABSTRACT The present work involves the formulation of colon targeted matrix tablet of Mesalazine by using direct compression method. Excipients including in the formulation are Eudragit S100, Ethyl cellulose, Lactose, Talc, Magnesium stearate. Preformulation studies have also been performed to study the nature of API and compatibility of API with excipients by physical observation and TLC studies. The result showed that API was compatible with all the excipients selected. The tablets were formulated by direct compression method using the selected excipient quantities. The formulated tablets we
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K. Sunil kumar, R. G. Chandrakala, A. R. Sravanthi, P. Swarna latha, D. peeravali, and A. Vamsi. "Formulation and evaluation of colon targeted matrix tablet of ibuprofen." World Journal of Advanced Research and Reviews 18, no. 2 (2023): 519–35. http://dx.doi.org/10.30574/wjarr.2023.18.2.0562.

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The present work involves the formulation of colon targeted matrix tablet of Ibuprofen by using direct compression method. Literatures regarding, Ibuprofen tablet dosage form preparation, excipients selection, manufacturing method etc., has been collected and reviewed. In this work, selection of excipients was done based on a literature review. Excipients include Eudragit S100, Ethyl cellulose, Lactose, Talc, Magnesium stearate. Quantities of the excipients were selected performing FT-IR method which is an HIS of Fourrts India Laboratory. Preformulation studies have also been performed to stud
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K., Sunil kumar, G. Chandrakala R., R. Sravanthi A., Swarna latha P., peeravali D., and Vamsi A. "Formulation and evaluation of colon targeted matrix tablet of ibuprofen." World Journal of Advanced Research and Reviews 18, no. 2 (2023): 519–35. https://doi.org/10.5281/zenodo.8404828.

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The present work involves the formulation of colon targeted matrix tablet of Ibuprofen by using direct compression method. Literatures regarding, Ibuprofen tablet dosage form preparation, excipients selection, manufacturing method etc., has been collected and reviewed. In this work, selection of excipients was done based on a literature review. Excipients include Eudragit S100, Ethyl cellulose, Lactose, Talc, Magnesium stearate. Quantities of the excipients were selected performing FT-IR method which is an HIS of Fourrts India Laboratory. Preformulation studies have also been performed to stud
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Vemula, Sateesh Kumar, and Vijaya Kumar Bontha. "Colon Targeted Guar Gum Compression Coated Tablets of Flurbiprofen: Formulation, Development, and Pharmacokinetics." BioMed Research International 2013 (2013): 1–8. http://dx.doi.org/10.1155/2013/287919.

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The rationale of the present study is to formulate flurbiprofen colon targeted compression coated tablets using guar gum to improve the therapeutic efficacy by increasing drug levels in colon, and also to reduce the side effects in upper gastrointestinal tract. Direct compression method was used to prepare flurbiprofen core tablets, and they were compression coated with guar gum. Then the tablets were optimized with the support ofin vitrodissolution studies, and further it was proved by pharmacokinetic studies. The optimized formulation (F4) showed almost complete drug release in the colon (99
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N, Audinarayana, Anala Srinivasulu, Vellore Sruthikumari, Likitha, and Ananda Deepak V. "Colon targeting oral matrix tablets of mesalamine: Design, development and invitro evaluation." International Journal of Novel Trends in Pharmaceutical Sciences 10, no. 1 (2020): 18–27. http://dx.doi.org/10.26452/ijntps.v10i1.1144.

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The principle in this present research is to formulate Mesalamine containing colon targeted tablets by using different polymers and evaluate the effect of different polymers in drug release pattern. The matrix tablets of Mesalamine are formulated by polysaccharides based polymers like Cellulose acetate phthalate (CAP), Ethyl cellulose (EC), Guar gum (GG) and Xanthan gum (XG) which protects the drug to release in Stomach and Small Intestine. The invitro drug dissolution investigation of F2 (GG and XG) Matrix tablet was controlled by swelling into a viscous gel in colonic pH, which have been acc
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MD, Rawoof, Rajnarayana K, and Ajitha M. "Development and In Vivo Evaluation of Mesalazine Colon Targeted Tablets." International Journal of Pharmaceutical Sciences and Nanotechnology 12, no. 3 (2019): 4552–58. http://dx.doi.org/10.37285/ijpsn.2019.12.3.6.

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The main objective of the present study was to develop colon-targeted tablets of mesalazine by wet granulation method using 33 Response surface method with design of experiment software and HPMC K4M, Eudragit RL100, Ethyl cellulose and PVP K-30 used as pH dependent polymers. All the formulations (F1 to F27) were evaluated for the physicochemical parameters and were subjected to in vitro drug release studies. The amount of Mesalazine released from tablets at different time intervals was estimated by UV spectrophotometer. The formulation F26 released 98.16 % of mesalazine after 24 h, whereas mar
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Godge, GR, and SN Hiremath. "Development and evaluation of colon targeted drug delivery system by using natural Polysaccharides/Polymers." Dhaka University Journal of Pharmaceutical Sciences 13, no. 1 (2015): 105–13. http://dx.doi.org/10.3329/dujps.v13i1.21874.

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Colon is being extensively investigated as a drug delivery site. This study contains comparison of the usual enteric coating polymers viz. xanthan gum, guar gum, chitosan and ethyl cellulose, as carriers for colon specific drug delivery. Lactose based metoprolol succinate tablets were prepared. These were coated with one of the coating polymers to a varying coat thickness. Tablets were prepared using polysaccharides or synthetic polymer as binders. These included xanthan gum, guar gum, chitosan and ethyl cellulose. Metoprolol Succinate was used as a model drug. The prepared tablets were enteri
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Mobarak, Hussain, Das Biswajit, and Chakraborty Jashabir. "Formulation, Optimization and Evaluation of Capecitabine Tablet for Colon Specific Drug Delivery System." INTERNATIONAL JOURNAL OF PHARMACEUTICAL AND CLINICAL RESEARCH 09, no. 07 (2017): 539–49. https://doi.org/10.25258/ijpcr.v9i7.8788.

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Aim: The present research is focused on development and optimization of colon specific, fast disintegrating Capecitabine tablet for the treatment of Colon cancer. Methods: Colon targeted core tablet of Capecitabine was prepared by using CCS (Croscarmellose sodium) as a super disintegrating agent by direct compression method and coating was done over the core tablets by using pectin in different ratios by compression coating method. The colon targeted coating was done on the compression coated tablets by using ES100 and CAP (Cellulose acetate phthalate) in different ratios by dip coating method
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Vivekanandan, K. 1. *. Dr. Gunasekaran V. 2. "FORMULATION AND EVALUATION OF COLON TARGETED MATRIX FORMULATIONS OF BUDESONIDE OF PREDNISOLONE." Journal of Scientific Research in Pharmacy 7, no. 9 (2018): 96–101. https://doi.org/10.5281/zenodo.1421246.

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<strong><em>ABSTARCT</em></strong> <strong><em>I</em></strong><em>n the present research work sustained release matrix formulation of Budesonide targeted to colon by using various polymers developed. </em><em>Budesonide is a selective cyclooxygenase-2 inhibitor with pH-dependent solubility. To achieve pH-independent drug release of budesonide, pH modifying agents (buffering agents) were used. Colon targeted tablets were prepared in two steps. Initially core tablets were prepared and then the tablets were coated by using different pH dependent polymers. Ethyl cellulose, Eudragit L100 and S100 w
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Części książek na temat "Colon targeted tablets"

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Enoki, Toshiaki, Morinobu Endo, and Masatsugu Suzuki. "Synthesis and Intercalation Chemistry." In Graphite Intercalation Compounds and Applications. Oxford University Press, 2003. http://dx.doi.org/10.1093/oso/9780195128277.003.0004.

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Alkali metal GICs are the best known donor type GICs, since they are easily prepared and their brilliant gold color for stage-1 GICs has attracted scientists working in intercalation chemistry. They have therefore been targets of intensive and detailed studies of their solid-state properties on the basis of the employment of highly oriented pyrolytic graphite (HOPG). There are several intercalation methods, which are classified basically into vapor-phase reaction, reaction of the mixture of graphite and alkali metal, high pressure reaction, electrochemical reaction, and reaction in a solvent.
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Streszczenia konferencji na temat "Colon targeted tablets"

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Abdullah, A. "Machine Learning and Deep Learning for Digitizing Scanned Images of Seismic Reflection Data." In Indonesian Petroleum Association - 46th Annual Convention & Exhibition 2022. Indonesian Petroleum Association, 2022. http://dx.doi.org/10.29118/ipa22-g-99.

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We present the use of Machine Learning algorithm of K-Nearest Neighbors (KNN) and Deep Learning algorithm of Artificial Neural Network for converting scanned images of seismic reflection data into digital seismic format. Digital seismic data format provides more flexibility for users to implement seismic processing algorithms like de-noising, enhancement and converting it into standard format, namely SEGY for further analysis such as seismic interpretation and seismic attributes generation. Varieties of seismic image in color density representation with different color maps and conventional wi
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Wang, Lihua, Wanming Liu, and Wenying Tian. "Target Search Algorithms Based on the Dynamic Window and Color Index Table Combination." In 2012 4th International Conference on Intelligent Human-Machine Systems and Cybernetics (IHMSC). IEEE, 2012. http://dx.doi.org/10.1109/ihmsc.2012.64.

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Nevoso, Isabella, Niccolò Casiddu, Annapaola Vacanti, Claudia Porfirione, Isabel Leggiero, and Francesco Burlando. "HCD methodologies and simulation for visual rehabilitator’s education in oMERO project." In 9th International Conference on Human Interaction and Emerging Technologies - Artificial Intelligence and Future Applications. AHFE International, 2023. http://dx.doi.org/10.54941/ahfe1002923.

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Objectives:The presented work arises in the context of designing for individuals with visual impairment, specifically we refer to a target group of children from two to seven years of age. The study was conducted with the contribution of the XXX research group within the XXX project funded by the European Community (2020-2023), with the aim of creating a specific curriculum for training the profession of a visual rehabilitator for children. In this perspective, the paper shows a practical case study carried out through the simulation technique at XXX.The approach that would be applied to this
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Raporty organizacyjne na temat "Colon targeted tablets"

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Ley, Matt, Tom Baldvins, David Jones, Hanna Pilkington, and Kelly Anderson. Vegetation classification and mapping: Gulf Islands National Seashore. National Park Service, 2023. http://dx.doi.org/10.36967/2299028.

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The Gulf Islands National Seashore (GUIS) vegetation inventory project classified and mapped vegetation on park-owned lands within the administrative boundary and estimated thematic map accuracy quantitatively. The project began in June 2016. National Park Service (NPS) Vegetation Mapping Inventory Program provided technical guidance. The overall process included initial planning and scoping, imagery procurement, field data collection, data analysis, imagery interpretation/classification, accuracy assessment (AA), and report writing and database development. Initial planning and scoping meetin
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Ley, Matt, Tom Baldvins, Hannah Pilkington, David Jones, and Kelly Anderson. Vegetation classification and mapping project: Big Thicket National Preserve. National Park Service, 2024. http://dx.doi.org/10.36967/2299254.

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The Big Thicket National Preserve (BITH) vegetation inventory project classified and mapped vegetation within the administrative boundary and estimated thematic map accuracy quantitatively. National Park Service (NPS) Vegetation Mapping Inventory Program provided technical guidance. The overall process included initial planning and scoping, imagery procurement, vegetation classification field data collection, data analysis, imagery interpretation/classification, accuracy assessment (AA), and report writing and database development. Initial planning and scoping meetings took place during May, 2
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